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||||||||||| ReadSeq supported formats (revised 30Dec92)
--------------------------------------------------------
-f[ormat=]Name Format name for output:
1. IG/Stanford 10. Olsen (in-only)
2. GenBank/GB 11. Phylip3.2
3. NBRF 12. Phylip
4. EMBL 13. Plain/Raw
5. GCG 14. PIR/CODATA
6. DNAStrider 15. MSF
7. Fitch 16. ASN.1
8. Pearson/Fasta 17. PAUP
9. Zuker (in-only) 18. Pretty (out-only)
In general, output supports only minimal subsets of each format
needed for sequence data exchanges. Features, descriptions
and other format-unique information is discarded.
Users of Olsen multi sequence editor (VMS). The Olsen format
here is produced with the print command:
print/out=some.file
Use Genbank output from readseq to produce a format that this
editor can read, and use the command
load/genbank some.file
Dan Davison has a VMS program that will convert to/from the
Olsen native binary data format. E-mail davison@uh.edu
Warning: Phylip format input is now supported (30Dec92), however the
auto-detection of Phylip format is very probabilistic and messy,
especially distinguishing sequential from interleaved versions. It
is not recommended that one use readseq to convert files from Phylip
format to others unless essential.
||||||||||| ReadSeq usage (revised 11Nov91)
--------------------------------------------------------
A. determine file format:
short skiplines; /* result: number of header lines to skip (or 0) */
short error; /* error result or 0 */
short format; /* resulting format code, see ureadseq.h */
char *filename = "Mysequence.file"
format = seqFileFormat( filename, &skiplines, &error);
if (error!=0) fail;
B. read number and list of sequences (optional)
short numseqs; /* resulting number of sequences found in file */
char *seqlist; /* list of sequence names, newline separated, 0 terminated */
seqlist = listSeqs( filename, skiplines, format, &numseqs, &error);
if (error!=0) display (seqlist);
free( seqlist);
C. read individual sequences as desired
short seqIndex; /* sequence index #, or == kListSeqs for listSeqs equivalent */
long seqlen; /* length of seq */
char seqid[256]; /* sequence name */
char *seq; /* sequence, 0 terminated, free when done */
seq = readSeq( seqIndex, filename, skiplines, format,
&seqlen, &numseqs, &error, seqid);
if (error!=0) manipulate(seq);
free(seq);
D. write sequences as desired
int nlines; /* number of lines of sequence written */
FILE* fout; /* open file pointer (stdout or other) */
short outform; /* output format, see ureadseq.h */
nlines = writeSeq( fout, seq, seqlen, format, outform, seqid);
Note (30Dec92): There is various processing done by the main program (in readseq.c),
rather than just in the subroutines (in ureadseq.c). Especially for interleaved
output formats, the writeSeq subroutine does not handle interleaving, nor some of
the formatting at the top and end of output files. While seqFileFormat, listSeqs,
and readSeq subroutines are fairly self-contained, the writeSeq depends a lot on
auxilliary processing. At some point, this may be revised so writeSeq is self-
contained.
Note 2: The NCBI toolkit (ftp from ncbi.nlm.nih.gov) is needed for the ASN.1 format
reading (see ureadasn.c). A bastard (but workable I hope) ASN.1 format is written
by writeSeq alone.
||||||||||| sequence formats....
---------------------------------------------------
stanford/IG
;comments
;...
seq1 info
abcd...
efgh1 (or 2 = terminator)
;another seq
;....
seq2 info
abcd...1
--- for e.g. ----
; Dro5s-T.Seq Length: 120 April 6, 1989 21:22 Check: 9487 ..
dro5stseq
GCCAACGACCAUACCACGCUGAAUACAUCGGUUCUCGUCCGAUCACCGAAAUUAAGCAGCGUCGCGGGCG
GUUAGUACUUAGAUGGGGGACCGCUUGGGAACACCGCGUGUUGUUGGCCU1
; TOIG of: Dro5srna.Seq check: 9487 from: 1 to: 120
---------------------------------------------------
Genbank:
LOCUS seq1 ID..
...
ORIGIN ...
123456789abcdefg....(1st 9 columns are formatting)
hijkl...
// (end of sequence)
LOCUS seq2 ID ..
...
ORIGIN
abcd...
//
---------------------------------------------------
NBRF format: (from uwgcg ToNBRF)
>DL;DRO5SRNA
Iubio$Dua0:[Gilbertd.Gcg]Dro5srna.Seq;2 => DRO5SRNA
51 AAUUAAGCAG CGUCGCGGGC GGUUAGUACU UAGAUGGGGG ACCGCUUGGG
101 AACACCGCGU GUUGUUGGCC U
---------------------------------------------------
EMBL format
ID345 seq1 id (the 345 are spaces)
... other info
SQ345Sequence (the 3,4,5 are spaces)
abcd...
hijk...
// (! this is proper end string: 12Oct90)
ID seq2 id
...
SQ Sequence
abcd...
...
//
---------------------------------------------------
UW GCG Format:
comments of any form, up to ".." signal
signal line has seq id, and " Check: #### .."
only 1 seq/file
-- e.g. --- (GCG from GenBank)
LOCUS DROEST6 1819 bp ss-mRNA INV 31-AUG-1987
... much more ...
ORIGIN 1 bp upstream of EcoRI site; chromosome BK9 region 69A1.
INVERTEBRATE:DROEST6 Length: 1819 January 9, 1989 16:48 Check: 8008 ..
1 GAATTCGCCG GAGTGAGGAG CAACATGAAC TACGTGGGAC TGGGACTTAT
51 CATTGTGCTG AGCTGCCTTT GGCTCGGTTC GAACGCGAGT GATACAGATG
---------------------------------------------------
DNAStrider (Mac) = modified Stanford:
; ### from DNA Strider Friday, April 7, 1989 11:04:24 PM
; DNA sequence pBR322 4363 b.p. complete sequence
;
abcd...
efgh
// (end of sequence)
---------------------------------------------------
Fitch format:
Dro5srna.Seq
GCC AAC GAC CAU ACC ACG CUG AAU ACA UCG GUU CUC GUC CGA UCA CCG AAA UUA AGC AGC
GUC GCG GGC GGU UAG UAC UUA GAU GGG GGA CCG CUU GGG AAC ACC GCG UGU UGU UGG CCU
Droest6.Seq
GAA TTC GCC GGA GTG AGG AGC AAC ATG AAC TAC GTG GGA CTG GGA CTT ATC ATT GTG CTG
AGC TGC CTT TGG CTC GGT TCG AAC GCG AGT GAT ACA GAT GAC CCT CTG TTG GTG CAG CTG
---------------------------------------------------
W.Pearson/Fasta format:
>BOVPRL GenBank entry BOVPRL from omam file. 907 nucleotides.
TGCTTGGCTGAGGAGCCATAGGACGAGAGCTTCCTGGTGAAGTGTGTTTCTTGAAATCAT
---------------------------------------------------
Phylip version 3.2 format (e.g., DNAML):
5 13 YF (# seqs, #bases, YF)
Alpha AACGTGGCCAAAT
aaaagggccc... (continued sp. alpha)
Beta AAGGTCGCCAAAC
aaaagggccc... (continued sp. beta)
Gamma CATTTCGTCACAA
aaaagggccc... (continued sp. Gamma)
1234567890^-- bases must start in col 11, and run 'til #bases
(spaces & newlines are okay)
---------------------------------------------------
Phylip version 3.3 format (e.g., DNAML):
5 42 YF (# seqs, #bases, YF)
Turkey AAGCTNGGGC ATTTCAGGGT
Salmo gairAAGCCTTGGC AGTGCAGGGT
H. SapiensACCGGTTGGC CGTTCAGGGT
Chimp AAACCCTTGC CGTTACGCTT
Gorilla AAACCCTTGC CGGTACGCTT
1234567890^-- bases must start in col 11
!! this version interleaves the species -- contrary to
all other output formats.
GAGCCCGGGC AATACAGGGT AT
GAGCCGTGGC CGGGCACGGT AT
ACAGGTTGGC CGTTCAGGGT AA
AAACCGAGGC CGGGACACTC AT
AAACCATTGC CGGTACGCTT AA
---------------------------------------------------
Phylip version 3.4 format (e.g., DNAML)
-- Both Interleaved and sequential are permitted
5 13 (# seqs, #bases)
Alpha AACGTGGCCAAAT
aaaagggccc... (continued sp. alpha)
Beta AAGGTCGCCAAAC
aaaagggccc... (continued sp. beta)
Gamma CATTTCGTCACAA
aaaagggccc... (continued sp. Gamma)
1234567890^-- bases must start in col 11, and run 'til #bases
(spaces, newlines and numbers are are ignored)
---------------------------------------------------
Gary Olsen (multiple) sequence editor /print format:
!---------------------
!17Oct91 -- error in original copy of olsen /print format, shifted right 1 space
! here is correct copy:
301 40 Tb.thiop CGCAGCGAAA----------GCUNUGCUAAUACCGCAUA-CGnCCUG----------------------------------------------------- Tb.thiop
123456789012345678901
301 42 Rhc.purp CGUAGCGAAA----------GUUACGCUAAUACCGCAUA-UUCUGUG----------------------------------------------------- Rhc.purp
301 44 Rhc.gela nnngnCGAAA----------GCCGGAUUAAUACCGCAUA-CGACCUA----------------------------------------------------- Rhc.gela
!---------------------
RNase P RNA components. on 20-FEB-90 17:23:58
1 (E.c. pr ): Base pairing in Escherichia coli RNase P RNA.
2 (chrom ): Chromatium
:
12 (B.brevis): Bacillus brevis RNase P RNA, B. James.
13 ( 90% con): 90% conserved
14 (100% con): 100% conserved
15 (gram+ pr): pairing
1
RNase P RNA components. on 20-FEB-90 17:23:58
Posi- Sequence
tion: identity: Data:
1 1 E.c. pr <<<<<<<<<< {{{{{{{{<<:<<<<<<<<<<^<<<<<<====>>>> E.c. pr
1 2 chrom GGAGUCGGCCAGACAGUCGCUUCCGUCCU------------------ chrom
:
1 12 B.brevis AUGCAGGAAAUGCGGGUAGCCGCUGCCGCAAUCGUCU------------- B.brevis
1234567890123456789012 <! this should be 21 not 22,
! this example must be inset on left by 1 space from olsen /print files !
1 13 90% con G C G A CGC GC - - 90% con
1 14 100% con G A CGC 100% con
1 15 gram+ pr <<<<<<<<<< {{{{{{{{<<<<<<<<<<<<<=============== gram+ pr
60 1 E.c. pr >>>>>>^>>^>>>>:>> <<<^<<<< {{{{{ E.c. pr
60 2 chrom -----GGUG-ACGGGGGAGGAAAGUCCGG-GCUCCAU------------- chrom
: :
60 10 B.stearo ----UU-CG-GCCGUAGAGGAAAGUCCAUGCUCGCACGGUGCUGAGAUGC B.stearo
---------------------------------------------------
GCG MSF format
Title line
picorna.msf MSF: 100 Type: P January 17, 1991 17:53 Check: 541
..
Name: Cb3 Len: 100 Check: 7009 Weight: 1.00
Name: E Len: 100 Check: 60 Weight: 1.00
//
1 50
Cb3 ...gpvedai .......t.. aaigr..vad tvgtgptnse aipaltaaet
E gvenae.kgv tentna.tad fvaqpvylpe .nqt...... kv.affynrs
51 100
Cb3 ghtsqvvpgd tmqtrhvkny hsrsestien flcrsacvyf teykn.....
E ...spi.gaf tvks...... gs.lesgfap .fsngtc.pn sviltpgpqf
---------------------------------------------------
PIR format
This is NBRF-PIR MAILSERVER version 1.45
Command-> get PIR3:A31391
\\\
ENTRY A31391 #Type Protein
TITLE *Esterase-6 - Fruit fly (Drosophila melanogaster)
DATE 03-Aug-1992 #Sequence 03-Aug-1992 #Text 03-Aug-1992
PLACEMENT 0.0 0.0 0.0 0.0 0.0
COMMENT *This entry is not verified.
SOURCE Drosophila melanogaster
REFERENCE
#Authors Cooke P.H., Oakeshott J.G.
#Citation submitted to GenBank, April 1989
#Reference-number A31391
#Accession A31391
#Cross-reference GB:J04167
SUMMARY #Molecular-weight 61125 #Length 544 #Checksum 1679
SEQUENCE
5 10 15 20 25 30
1 M N Y V G L G L I I V L S C L W L G S N A S D T D D P L L V
31 Q L P Q G K L R G R D N G S Y Y S Y E S I P Y A E P P T G D
61 L R F E A P E P Y K Q K W S D I F D A T K T P V A C L Q W D
91 Q F T P G A N K L V G E E D C L T V S V Y K P K N S K R N S
121 F P V V A H I H G G A F M F G A A W Q N G H E N V M R E G K
151 F I L V K I S Y R L G P L G F V S T G D R D L P G N Y G L K
181 D Q R L A L K W I K Q N I A S F G G E P Q N V L L V G H S A
211 G G A S V H L Q M L R E D F G Q L A R A A F S F S G N A L D
241 P W V I Q K G A R G R A F E L G R N V G C E S A E D S T S L
271 K K C L K S K P A S E L V T A V R K F L I F S Y V P F A P F
301 S P V L E P S D A P D A I I T Q D P R D V I K S G K F G Q V
331 P W A V S Y V T E D G G Y N A A L L L K E R K S G I V I D D
361 L N E R W L E L A P Y L L F Y R D T K T K K D M D D Y S R K
391 I K Q E Y I G N Q R F D I E S Y S E L Q R L F T D I L F K N
421 S T Q E S L D L H R K Y G K S P A Y A Y V Y D N P A E K G I
451 A Q V L A N R T D Y D F G T V H G D D Y F L I F E N F V R D
481 V E M R P D E Q I I S R N F I N M L A D F A S S D N G S L K
511 Y G E C D F K D N V G S E K F Q L L A I Y I D G C Q N R Q H
541 V E F P
///
\\\
---------------------------------------------------
PAUP format:
The NEXUS Format
Every block starts with "BEGIN blockname;" and ends with "END;".
Each block is composed of one or more statements, each
terminated by a semicolon (;).
Comments may be included in NEXUS files by enclosing them within
square brackets, as in "[This is a comment]."
NEXUS-conforming files are identified by a "#NEXUS" directive at
the very beginning of the file (line 1, column 1). If the
#NEXUS is omitted PAUP issues a warning but continues
processing.
NEXUS files are entirely free-format. Blanks, tabs, and
newlines may be placed anywhere in the file. Unless RESPECTCASE
is requested, commands and data may be entered in upper case,
lower case, or a mixture of upper and lower case.
The following conventions are used in the syntax descriptions of
the various blocks. Upper-case items are entered exactly as
shown. Lower-case items inside of angle brackets -- e.g., <x>
-- represent items to be substituted by the user. Items inside
of square brackets -- e.g., [X] -- are optional. Items inside
of curly braces and separated by vertical bars -- e.g., { X | Y
| Z } -- are mutually exclusive options.
The DATA Block
The DATA block contains the data matrix and other associated
information. Its syntax is:
BEGIN DATA;
DIMENSIONS NTAX=<number of taxa> NCHAR=<number of characters>;
[ FORMAT [ MISSING=<missing-symbol> ]
[ LABELPOS={ LEFT | RIGHT } ]
[ SYMBOLS="<symbols-list>" ]
[ INTERLEAVE ]
[ MATCHCHAR=<match-symbol> ]
[ EQUATE="<symbol>=<expansion> [<symbol>=<expansion>...]" ]
[ TRANSPOSE ]
[ RESPECTCASE ]
[ DATATYPE = { STANDARD | DNA | RNA | PROTEIN } ]; ]
[ OPTIONS [ IGNORE={ INVAR | UNINFORM } ]
[ MSTAXA = { UNCERTAIN | POLYMORPH | VARIABLE } ]
[ ZAP = "<list of zapped characters>" ] ; ]
[ CHARLABELS <label_1> label_2><3E><> <label_NCHAR> ; ]
[ TAXLABELS <label1_1> <label1_2> <label1_NTAX> ; ]
[ STATELABELS <currently ignored by PAUP> ; ]
MATRIX <data-matrix> ;
END;
--- example PAUP file
#NEXUS
[!Brown et al. (1982) primate mitochondrial DNA]
begin data;
dimensions ntax=5 nchar=896;
format datatype=dna matchchar=. interleave missing='-';
matrix
[ 2 4 6 8 ]
[ 1 1 1 1 1 ]
human aagcttcaccggcgcagtca ttctcataatcgcccacggR cttacatcctcattactatt ctgcctagcaaactcaaact acgaacgcactcacagtcgc
chimp ................a.t. .c.................a ...............t.... ..................t. .t........c.........
gorilla ..................tg ....t.....t........a ........a......t.... .................... .......a..c.....c...
orang ................ac.. cc.....g..t.....t..a ..c........cc....g.. .................... .......a..c.....c...
gibbon ......t..a..t...ac.g .c.................a ..a..c..t..cc.g..... ......t............. .......a........c...
[ 8 8 8 8 8 8 ]
[ 0 2 4 6 8 9 ]
[ 1 1 1 1 1 6 ]
human cttccccacaacaatattca tgtgcctagaccaagaagtt attatctcgaactgacactg agccacaacccaaacaaccc agctctccctaagctt
chimp t................... .a................c. ........a.....g..... ...a................ ................
gorilla ..................tc .a................c. ........a.g......... ...a.............tt. .a..............
orang ta....a...........t. .c.......ga......acc ..cg..a.a......tg... .a.a..c.....g...cta. .a.....a........
gibbon a..t.......t........ ....ac...........acc .....t..a........... .a.tg..........gctag .a..............
;
end;
---------------------------------------------------
||||||||||| Sample SMTP mail header
---------------------------------------------------
- - - - - - - - -
From GenBank-Retrieval-System@genbank.bio.net Sun Nov 10 17:28:56 1991
Received: from genbank.bio.net by sunflower.bio.indiana.edu
(4.1/9.5jsm) id AA19328; Sun, 10 Nov 91 17:28:55 EST
Received: by genbank.bio.net (5.65/IG-2.0)
id AA14458; Sun, 10 Nov 91 14:30:03 -0800
Date: Sun, 10 Nov 91 14:30:03 -0800
Message-Id: <9111102230.AA14458@genbank.bio.net>
From: Database Server <GenBank-Retrieval-System@genbank.bio.net>
To: gilbertd@sunflower.bio.indiana.edu
Subject: Results of Query for drorna
Status: R
No matches on drorna.
- - - - - -
From GenBank-Retrieval-System@genbank.bio.net Sun Nov 10 17:28:49 1991
Received: from genbank.bio.net by sunflower.bio.indiana.edu
(4.1/9.5jsm) id AA19323; Sun, 10 Nov 91 17:28:47 EST
Received: by genbank.bio.net (5.65/IG-2.0)
id AA14461; Sun, 10 Nov 91 14:30:03 -0800
Date: Sun, 10 Nov 91 14:30:03 -0800
Message-Id: <9111102230.AA14461@genbank.bio.net>
From: Database Server <GenBank-Retrieval-System@genbank.bio.net>
To: gilbertd@sunflower.bio.indiana.edu
Subject: Results of Query for droest6
Status: R
LOCUS DROEST6 1819 bp ss-mRNA INV 31-AUG-1987
DEFINITION D.melanogaster esterase-6 mRNA, complete cds.
ACCESSION M15961
||||||||||| GCG manual discussion of sequence symbols:
---------------------------------------------------
III_SEQUENCE_SYMBOLS
GCG programs allow all upper and lower case letters, periods (.),
asterisks (*), pluses (+), ampersands (&), and ats (@) as symbols in
biological sequences. Nucleotide symbols, their complements, and the
standard one-letter amino acid symbols are shown below in separate lists.
The meanings of the symbols +, &, and @ have not been assigned at this
writing (March, 1989).
GCG uses the letter codes for amino acid codes and nucleotide
ambiguity proposed by IUB (Nomenclature Committee, 1985,
Eur. J. Biochem. 150; 1-5). These codes are compatible with the codes
used by the EMBL, GenBank, and NBRF data libraries.
NUCLEOTIDES
The meaning of each symbol, its complement, and the Cambridge and
Stanford equivalents are shown below. Cambridge files can be converted
into GCG files and vice versa with the programs FROMSTADEN and TOSTADEN.
IntelliGenetics sequence files can be interconverted with the programs
FROMIG and TOIG.
IUB/GCG Meaning Complement Staden/Sanger Stanford
A A T A A
C C G C C
G G C G G
T/U T A T T/U
M A or C K 5 J
R A or G Y R R
W A or T W 7 L
S C or G S 8 M
Y C or T R Y Y
K G or T M 6 K
V A or C or G B not supported N
H A or C or T D not supported N
D A or G or T H not supported N
B C or G or T V not supported N
X/N G or A or T or C X -/X N
. not G or A or T or C . not supported ?
The frame ambiguity codes used by Staden are not supported by GCG
and are translated by FROMSTADEN as the lower case single base
equivalent.
Staden Code Meaning GCG
D C or CC c
V T or TT t
B A or AA a
H G or GG g
K C or CX c
L T or TX t
M A or AX a
N G or GX g
AMINO ACIDS
Here is a list of the standard one-letter amino acid codes and their
three-letter equivalents. The synonymous codons and their depiction in
the IUB codes are shown. You should recognize that the codons following
semicolons (;) are not sufficiently specific to define a single amino
acid even though they represent the best possible back translation into
the IUB codes! All of the relationships in this list can be redefined by
the user in a local data file described below.
IUB
Symbol 3-letter Meaning Codons Depiction
A Ala Alanine GCT,GCC,GCA,GCG !GCX
B Asp,Asn Aspartic,
Asparagine GAT,GAC,AAT,AAC !RAY
C Cys Cysteine TGT,TGC !TGY
D Asp Aspartic GAT,GAC !GAY
E Glu Glutamic GAA,GAG !GAR
F Phe Phenylalanine TTT,TTC !TTY
G Gly Glycine GGT,GGC,GGA,GGG !GGX
H His Histidine CAT,CAC !CAY
I Ile Isoleucine ATT,ATC,ATA !ATH
K Lys Lysine AAA,AAG !AAR
L Leu Leucine TTG,TTA,CTT,CTC,CTA,CTG
!TTR,CTX,YTR;YTX
M Met Methionine ATG !ATG
N Asn Asparagine AAT,AAC !AAY
P Pro Proline CCT,CCC,CCA,CCG !CCX
Q Gln Glutamine CAA,CAG !CAR
R Arg Arginine CGT,CGC,CGA,CGG,AGA,AGG
!CGX,AGR,MGR;MGX
S Ser Serine TCT,TCC,TCA,TCG,AGT,AGC !TCX,AGY;WSX
T Thr Threonine ACT,ACC,ACA,ACG !ACX
V Val Valine GTT,GTC,GTA,GTG !GTX
W Trp Tryptophan TGG !TGG
X Xxx Unknown !XXX
Y Tyr Tyrosine TAT, TAC !TAY
Z Glu,Gln Glutamic,
Glutamine GAA,GAG,CAA,CAG !SAR
* End Terminator TAA, TAG, TGA !TAR,TRA;TRR
||||||||||| docs from PSC on sequence formats:
---------------------------------------------------
Nucleic Acid and Protein Sequence File Formats
It will probably save you some time if you have your data in a usable
format before you send it to us. However, we do have the University of
Wisconsin Genetics Computing Group programs running on our VAXen and
this package includes several reformatting utilities. Our programs
usually recognize any of several standard formats, including GenBank,
EMBL, NBRF, and MolGen/Stanford. For the purposes of annotating an
analysis we find the GenBank and EMBL formats most useful, particularly
if you have already received an accession number from one of these
organizations for your sequence.
Our programs do not require that all of the line types available in
GenBank, EMBL, or NBRF file formats be present for the file format to
be recognized and processed. The following pages outline the essential
details required for correct processing of files by our programs.
Additional information may be present but will generally be ignored.
GenBank File Format
File Header
1. The first line in the file must have "GENETIC SEQUENCE DATA BANK"
in spaces 20 through 46 (see LINE 1, below).
2. The next 8 lines may contain arbitrary text. They are ignored but
are required to maintain the GenBank format (see LINE 2 - LINE 9).
Sequence Data Entries
3. Each sequence entry in the file should have the following format.
a) first line: Must have LOCUS in the first 5 spaces. The
genetic locus name or identifier must be in spaces
13 - 22. The length of the sequences is right
justified in spaces 23 through 29 (see LINE 10).
b) second line: Must have DEFINITION in the first 10 spaces.
Spaces 13 - 80 are free form text to identify the
sequence (see LINE 11).
c) third line: Must have ACCESSION in the first 9 spaces. Spaces
13 - 18 must hold the primary accession number
(see LINE 12).
d) fourth line: Must have ORIGIN in the first 6 spaces. Nothing
else is required on this line, it indicates that
the nucleic acid sequence begins on the next line
(see LINE 13).
e) fifth line: Begins the nucleotide sequence. The first 9
spaces of each sequence line may either be blank
or may contain the position in the sequence of the
first nucleotide on the line. The next 66 spaces
hold the nucleotide sequence in six blocks of ten
nucleotides. Each of the six blocks begins with a
blank space followed by ten nucleotides. Thus the
first nucleotide is in space eleven of the line while
the last is in space 75 (see LINE 14, LINE 15).
f) last line: Must have // in the first 2 spaces to indicate
termination of the sequence (see LINE 16).
NOTE: Multiple sequences may appear in each file. To begin another
sequence go back to a) and start again.
Example GenBank file
LINE 1 : GENETIC SEQUENCE DATA BANK
LINE 2 :
LINE 3 :
LINE 4 :
LINE 5 :
LINE 6 :
LINE 7 :
LINE 8 :
LINE 9 :
LINE 10 :LOCUS L_Name Length BP
LINE 11 :DEFINITION Describe the sequence any way you want
LINE 12 :ACCESSION Accession Number
LINE 13 :ORIGIN
LINE 14 : 1 acgtacgtac gtacgtacgt acgtacgtac gtacgtacgt a...
LINE 15 : 61 acgt...
LINE 16 ://
EMBL File Format
Unlike the GenBank file format the EMBL file format does not require
a series of header lines. Thus the first line in the file begins
the first sequence entry of the file.
1. The first line of each sequence entry contains the two letters ID
in the first two spaces. This is followed by the EMBL identifier
in spaces 6 through 14. (See LINE 1).
2. The second line of each sequence entry has the two letters AC in
the first two spaces. This is followed by the accession number in
spaces 6 through 11. (See LINE 2).
3. The third line of each sequence entry has the two letters DE in the
first two spaces. This is followed by a free form text definition
in spaces 6 through 72. (See LINE 3).
4. The fourth line in each sequence entry has the two letters SQ in
the first two spaces. This is followed by the length of the
sequence beginning at or after space 13. After the sequence length
there is a blank space and the two letters BP. (See LINE 4).
5. The nucleotide sequence begins on the fifth line of the sequence
entry. Each line of sequence begins with four blank spaces. The
next 66 spaces hold the nucleotide sequence in six blocks of ten
nucleotides. Each of the six blocks begins with a blank space
followed by ten nucleotides. Thus the first nucleotide is in space
6 of the line while the last is in space 70. (See LINE 5 -
LINE 6).
6. The last line of each sequence entry in the file is a terminator
line which has the two characters // in the first two spaces.
(See LINE 7).
7. Multiple sequences may appear in each file. To begin another
sequence go back to item 1 and start again.
Example EMBL file
LINE 1 :ID ID_name
LINE 2 :AC Accession number
LINE 3 :DE Describe the sequence any way you want
LINE 4 :SQ Length BP
LINE 5 : ACGTACGTAC GTACGTACGT ACGTACGTAC GTACGTA...
LINE 6 : ACGT...
LINE 7 ://
NBRF (protein or nucleic acid) File Format
1. The first line of each sequence entry begins with a greater than
symbol, >. This is immediately followed by the two character
sequence type specifier. Space four must contain a semi-colon.
Beginning in space five is the sequence name or identification code
for the NBRF database. The code is from four to six letters and
numbers. (See LINE 1).
!!!! >> add these to readseq
Specifier Sequence type
P1 protein, complete
F1 protein, fragment
DL DNA, linear
DC DNA, circular
RL RNA, linear
RC RNA, circular
N1 functional RNA, other than tRNA
N3 tRNA
2. The second line of each sequence entry contains two kinds of
information. First is the sequence name which is separated from
the organism or organelle name by the three character sequence
blank space, dash, blank space, " - ". There is no special
character marking the beginning of this line. (See LINE 2).
3. Either the amino acid or nucleic acid sequence begins on line three
and can begin in any space, including the first. The sequence is
free format and may be interrupted by blanks for ease of reading.
Protein sequences man contain special punctuation to indicate
various indeterminacies in the sequence. In the NBRF data files
all lines may be up to 500 characters long. However some PSC
programs currently have a limit of 130 characters per line
(including blanks), and BitNet will not accept lines of over eighty
characters. (See LINE 3, LINE 4, and LINE 5).
The last character in the sequence must be an asterisks, *.
Example NBRF file
LINE 1 :>P1;CBRT
LINE 2 :Cytochrome b - Rat mitochondrion (SGC1)
LINE 3 :M T N I R K S H P L F K I I N H S F I D L P A P S
LINE 4 : VTHICRDVN Y GWL IRY
LINE 5 :TWIGGQPVEHPFIIIGQLASISYFSIILILMPISGIVEDKMLKWN*
MolGen/Stanford File Format
1. The first line in a sequence file is a comment line. This line
begins with a semi-colon in the first space. This line need
not be present. If it is present it holds descriptive text.
There may be as many comment lines as desired at the first of
sequence file. (See LINE 1).
2. The second line must be present and contains an identifier or
name for the sequence in the first ten spaces. (See LINE 2).
3. The sequence begins on the third line and occupies up to eighty
spaces. Spaces may be included in the sequence for ease of
reading. The sequence continues for as many line as needed
and is terminated with a 1 or 2. 1 indicates a linear sequence
while 2 marks a circular sequence. (See LINE 3 and LINE 4).
Example MolGen/Stanford file
LINE 1 :; Describe the sequence any way you want
LINE 2 :ECTRNAGLY2
LINE 3 :ACGCACGTAC ACGTACGTAC A C G T C C G T ACG TAC GTA CGT
LINE 4 : GCTTA GG G C T A1
||||||||||| Phylip file format
---------------------------------------------------
Phylip 3.3 File Format (DNA sequences)
The input and output formats for PROTPARS and for RESTML are described in
their document files. In general their input formats are similar to those
described here, except that the one-letter codes for data are specific to those
programs and are described in those document files. Since the input formats
for the eight DNA sequence programs apply to all eight, they are described
here. Their input formats are standard: the data have A's, G's, C's and T's
(or U's). The first line of the input file contains the number of species and
the number of sites. As with the other programs, options information may
follow this. In the case of DNAML, DNAMLK, and DNADIST an additional line
(described in the document file for these pograms) may follow the first one.
Following this, each species starts on a new line. The first 10 characters of
that line are the species name. There then follows the base sequence of that
species, each character being one of the letters A, B, C, D, G, H, K, M, N, O,
R, S, T, U, V, W, X, Y, ?, or - (a period was also previously allowed but it is
no longer allowed, because it sometimes is used to in aligned sequences to mean
"the same as the sequence above"). Blanks will be ignored, and so will
numerical digits. This allows GENBANK and EMBL sequence entries to be read
with minimum editing.
These characters can be either upper or lower case. The algorithms
convert all input characters to upper case (which is how they are treated).
The characters constitute the IUPAC (IUB) nucleic acid code plus some slight
extensions. They enable input of nucleic acid sequences taking full account of
any ambiguities in the sequence.
The sequences can continue over multiple lines; when this is done the sequences
must be either in "interleaved" format, similar to the output of alignment
programs, or "sequential" format. These are described in the main document
file. In sequential format all of one sequence is given, possibly on multiple
lines, before the next starts. In interleaved format the first part of the
file should contain the first part of each of the sequences, then possibly a
line containing nothing but a carriage-return character, then the second part
of each sequence, and so on. Only the first parts of the sequences should be
preceded by names. Here is a hypothetical example of interleaved format:
5 42
Turkey AAGCTNGGGC ATTTCAGGGT
Salmo gairAAGCCTTGGC AGTGCAGGGT
H. SapiensACCGGTTGGC CGTTCAGGGT
Chimp AAACCCTTGC CGTTACGCTT
Gorilla AAACCCTTGC CGGTACGCTT
GAGCCCGGGC AATACAGGGT AT
GAGCCGTGGC CGGGCACGGT AT
ACAGGTTGGC CGTTCAGGGT AA
AAACCGAGGC CGGGACACTC AT
AAACCATTGC CGGTACGCTT AA
while in sequential format the same sequences would be:
5 42
Turkey AAGCTNGGGC ATTTCAGGGT
GAGCCCGGGC AATACAGGGT AT
Salmo gairAAGCCTTGGC AGTGCAGGGT
GAGCCGTGGC CGGGCACGGT AT
H. SapiensACCGGTTGGC CGTTCAGGGT
ACAGGTTGGC CGTTCAGGGT AA
Chimp AAACCCTTGC CGTTACGCTT
AAACCGAGGC CGGGACACTC AT
Gorilla AAACCCTTGC CGGTACGCTT
AAACCATTGC CGGTACGCTT AA
Note, of course, that a portion of a sequence like this:
300 AAGCGTGAAC GTTGTACTAA TRCAG
is perfectly legal, assuming that the species name has gone before, and is
filled out to full length by blanks. The above digits and blanks will be
ignored, the sequence being taken as starting at the first base symbol (in this
case an A).
The present versions of the programs may sometimes have difficulties with
the blank lines between groups of lines, and if so you might want to retype
those lines, making sure that they have only a carriage-return and no blank
characters on them, or you may perhaps have to eliminate them. The symptoms of
this problem are that the programs complain that the sequences are not properly
aligned, and you can find no other cause for this complaint.
------------------------------------------------
||||||||||| ASN.1 file format
---------------------------------------------------
ASN.1 -- see NCBI toolkit docs, source and examples (ncbi.nlm.nih.gov)
Example asn.1 sequence file----
Bioseq-set ::= {
seq-set {
seq {
id { local id 1 } , -- id essential
descr { title "Dummy sequence data from nowhere" } , -- optional
inst { -- inst essential
repr raw ,
mol dna ,
length 156 ,
topology linear ,
seq-data
iupacna "GAATTCATTTTTGAAACAAATCGACCTGACGACGGAATGGTACTCGAATTA
TGGGCCAAAGGGTTTTATGGGACAAATTAATAGGTGTTCATTATATGCCACTTTCGGAGATTAGATACAGCAATGCAG
TGGATTCAAAGCAATAGAGTTGTTCTT"
} } ,
seq {
id { local id 2 } ,
descr { title "Dummy sequence 2 data from somewhere else" } ,
inst {
repr raw ,
mol dna ,
length 150 ,
topology linear ,
seq-data
iupacna "TTTTTTTTTTTTGAAACAAATCGACCTGACGACGGAATGGTACTCGAATTA
TGGGCCAAAGGGTTTTATGGGACAAATTAATAGGTGTTCATTATATGCCACTTTCGGAGATTAGATACAGCAATGCAG
TGGATTCAAAGCAATAGAGTT"
}
}
}
}
partial ASN.1 description from toolkit
Bioseq ::= SEQUENCE {
id SET OF Seq-id , -- equivalent identifiers
descr Seq-descr OPTIONAL , -- descriptors
inst Seq-inst , -- the sequence data
annot SET OF Seq-annot OPTIONAL }
Seq-inst ::= SEQUENCE { -- the sequence data itself
repr ENUMERATED { -- representation class
not-set (0) , -- empty
virtual (1) , -- no seq data
raw (2) , -- continuous sequence
seg (3) , -- segmented sequence
const (4) , -- constructed sequence
ref (5) , -- reference to another sequence
consen (6) , -- consensus sequence or pattern
map (7) , -- ordered map (genetic, restriction)
other (255) } ,
mol ENUMERATED { -- molecule class in living organism
not-set (0) , -- > cdna = rna
dna (1) ,
rna (2) ,
aa (3) ,
na (4) , -- just a nucleic acid
other (255) } ,
length INTEGER OPTIONAL , -- length of sequence in residues
fuzz Int-fuzz OPTIONAL , -- length uncertainty
topology ENUMERATED { -- topology of molecule
not-set (0) ,
linear (1) ,
circular (2) ,
tandem (3) , -- some part of tandem repeat
other (255) } DEFAULT linear ,
strand ENUMERATED { -- strandedness in living organism
not-set (0) ,
ss (1) , -- single strand
ds (2) , -- double strand
mixed (3) ,
other (255) } OPTIONAL , -- default ds for DNA, ss for RNA, pept
seq-data Seq-data OPTIONAL , -- the sequence
ext Seq-ext OPTIONAL , -- extensions for special types
hist Seq-hist OPTIONAL } -- sequence history
------------------------------------------------

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$!
$!VAX-VMS cc make file for readseq
$!
$ echo := write sys$output
$ if p1.eqs."TEST" then goto tests
$
$ echo "compiling readseq..."
$ cc readseq, ureadseq
$!
$ echo "linking readseq..."
$ link readseq, ureadseq, sys$library:vaxcrtl/lib
$!
$tests:
$!
$ echo "defining readseq symbol:"
$ dd = f$environment("default")
$ readseq :== $ 'dd'readseq.exe
$ show symbol readseq
$!
$ echo ""
$ echo "test for general read/write of all chars:"
$ readseq -p alphabet.std -otest.alpha
$ diff test.alpha alphabet.std
$!
$ echo ""
$ echo "test for valid format conversions"
$!
$ readseq -v -p -f=ig nucleic.std -otest.ig
$ readseq -v -p -f=gb test.ig -otest.gb
$ readseq -v -p -f=nbrf test.gb -otest.nbrf
$ readseq -v -p -f=embl test.nbrf -otest.embl
$ readseq -v -p -f=gcg test.embl -otest.gcg
$ readseq -v -p -f=strider test.gcg -otest.strider
$ readseq -v -p -f=fitch test.strider -otest.fitch
$ readseq -v -p -f=fasta test.fitch -otest.fasta
$ readseq -v -p -f=pir test.fasta -otest.pir
$ readseq -v -p -f=ig test.pir -otest.ig-b
$ diff test.ig test.ig-b
$!
$ echo ""
$ echo "Test for multiple-sequence format conversions:"
$ readseq -p -f=ig multi.std -otest.m-ig
$ readseq -p -f=gb test.m-ig -otest.m-gb
$ readseq -p -f=nbrf test.m-gb -otest.m-nbrf
$ readseq -p -f=embl test.m-nbrf -otest.m-embl
$ readseq -p -f=fasta test.m-embl -otest.m-fasta
$ readseq -p -f=pir test.m-fasta -otest.m-pir
$ readseq -p -f=msf test.m-pir -otest.m-msf
$ readseq -p -f=paup test.m-msf -otest.m-paup
$ readseq -p -f=ig test.m-paup -otest.m-ig-b
$ diff test.m-ig test.m-ig-b
$ echo ""
$ echo "Expect differences in the header lines due to"
$ echo "different format headers. If any sequence lines"
$ echo "differ, or if checksums differ, there is a problem."
$!
$! #cleanup
$! delete test.*;
$ echo "-----------"
$ echo ""
$ echo "To clean up test files, command me:
$ echo " DELETE test.*;"
$!

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#
# Unix Makefile for readseq
# to use, command me:
# % make -- or --
# % make CC=your-c-compiler-name
#
# pick an ANSI C compiler (the default Sun CC is not ANSI)
CC=gcc # Gnu C Compiler
#CC=cc # SGI Irix
#CC=vcc # some DEC Ultrix
CFLAGS=
#CFLAGS= -DSMALLCHECKSUM # if you prefer to use a GCG-standard 13 bit checksum
# instead of a full 32 bit checksum. This may enhance compatibility w/ GCG software
SOURCES= readseq.c ureadseq.c ureadseq.h ureadasn.c
DOCS= Readme readseq.help Formats Stdfiles Makefile Make.com add.gdemenu *.std
# NCBI toolkit support for ASN.1 reader
# this is path to NCBI toolkit, you must set for your system:
NCBI=/bio/mb/ncbi
#
OTHERLIBS=-lm
LIB1=-lncbi
LIB2=-lncbiobj
LIB3=-lncbicdr
LIB4=-lvibrant
INCPATH=$(NCBI)/include
LIBPATH=$(NCBI)/lib
NCFLAGS=$(CFLAGS) -DNCBI -I$(INCPATH)
NLDFLAGS=-I$(INCPATH) -L$(LIBPATH)
NLIBS=$(LIB1) $(LIB2) $(OTHERLIBS)
all: build test
#build: $(SOURCES)
# @echo "Compiling readseq..."
# $(CC) $(CFLAGS) -o readseq readseq.c ureadseq.c
# if using NCBI, uncomment these lines in place of build: above
build: $(SOURCES)
@echo "Compiling readseq with NCBI toolkit support...";
$(CC) -o readseq $(NLDFLAGS) $(NCFLAGS) readseq.c ureadseq.c ureadasn.c $(NLIBS)
test: $(SOURCES) readseq
@echo ""
@echo "Test for general read/write of all chars:"
./readseq -p alphabet.std -otest.alpha
-diff test.alpha alphabet.std
@echo ""
@echo "Test for valid format conversions:"
./readseq -v -p -f=ig nucleic.std -otest.ig
./readseq -v -p -f=gb test.ig -otest.gb
./readseq -v -p -f=nbrf test.gb -otest.nbrf
./readseq -v -p -f=embl test.nbrf -otest.embl
./readseq -v -p -f=gcg test.embl -otest.gcg
./readseq -v -p -f=strider test.gcg -otest.strider
./readseq -v -p -f=fitch test.strider -otest.fitch
./readseq -v -p -f=fasta test.fitch -otest.fasta
./readseq -v -p -f=pir test.fasta -otest.pir
./readseq -v -p -f=ig test.pir -otest.ig-b
-diff test.ig test.ig-b
@echo ""
@echo "Test for multiple-sequence format conversions:"
./readseq -p -f=ig multi.std -otest.m-ig
./readseq -p -f=gb test.m-ig -otest.m-gb
./readseq -p -f=nbrf test.m-gb -otest.m-nbrf
./readseq -p -f=embl test.m-nbrf -otest.m-embl
./readseq -p -f=fasta test.m-embl -otest.m-fasta
./readseq -p -f=pir test.m-fasta -otest.m-pir
./readseq -p -f=msf test.m-pir -otest.m-msf
./readseq -p -f=paup test.m-msf -otest.m-paup
./readseq -p -f=ig test.m-paup -otest.m-ig-b
-diff test.m-ig test.m-ig-b
#
# if using NCBI, uncomment these lines
@echo ""
@echo "Test of NCBI ASN.1 conversions:"
./readseq -p -f=asn test.m-ig -otest.m-asn
./readseq -p -f=ig test.m-asn -otest.m-ig-c
-diff test.m-ig test.m-ig-c
#
@echo ""
@echo "Expect differences in the header lines due to"
@echo "different format headers. If any sequence lines"
@echo "differ, or if the checksums differ, there is a problem."
@echo "----------------------"
@echo ""
@echo "To clean up test files, command me:"
@echo " make clean"
clean:
rm -f *.o core test.*
shar:
@echo "shell archiving files..."
-rm -f readseq*.shar
mkdir readseqd
cp $(SOURCES) readseqd
cp $(DOCS) readseqd
shar -v readseqd > readseq.shar
rm -rf readseqd

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* ReadSeq -- 1 Feb 93
*
* Reads and writes nucleic/protein sequences in various
* formats. Data files may have multiple sequences.
*
* Copyright 1990 by d.g.gilbert
* biology dept., indiana university, bloomington, in 47405
* e-mail: gilbertd@bio.indiana.edu
*
* This program may be freely copied and used by anyone.
* Developers are encourged to incorporate parts in their
* programs, rather than devise their own private sequence
* format.
*
* This should compile and run with any ANSI C compiler.
* Please advise me of any bugs, additions or corrections.
Readseq has been updated. There have been a number of enhancements
and a few bug corrections since the previous general release in Nov 91
(see below). If you are using earlier versions, I recommend you update to
this release.
Readseq is particularly useful as it automatically detects many
sequence formats, and interconverts among them.
Formats added to this release include
+ MSF multi sequence format used by GCG software
+ PAUP's multiple sequence (NEXUS) format
+ PIR/CODATA format used by PIR
+ ASN.1 format used by NCBI
+ Pretty print with various options for nice looking output.
As well, Phylip format can now be used as input. Options to
reverse-compliment and to degap sequences have been added. A menu
addition for users of the GDE sequence editor is included.
This program is available thru Internet gopher, as
gopher ftp.bio.indiana.edu
browse into the IUBio-Software+Data/molbio/readseq/ folder
select the readseq.shar document
Or thru anonymous FTP in this manner:
my_computer> ftp ftp.bio.indiana.edu (or IP address 129.79.224.25)
username: anonymous
password: my_username@my_computer
ftp> cd molbio/readseq
ftp> get readseq.shar
ftp> bye
readseq.shar is a Unix shell archive of the readseq files.
This file can be editted by any text editor to reconstitute the
original files, for those who do not have a Unix system or an
Unshar program. Read the top of this .shar file for further
instructions.
There are also pre-compiled executables for the following computers:
Silicon Graphics Iris, Sparc (Sun Sparcstation & clones), VMS-Vax,
Macintosh. Use binary ftp to transfer these, except Macintosh. The
Mac version is just the command-line program in a window, not very
handy.
C source files:
readseq.c ureadseq.c ureadasn.c ureadseq.h
Document files:
Readme (this doc)
Readseq.help (longer than this doc)
Formats (description of sequence file formats)
add.gdemenu (GDE program users can add this to the .GDEmenu file)
Stdfiles -- test sequence files
Makefile -- Unix make file
Make.com -- VMS make file
*.std -- files for testing validity of readseq
Example usage:
readseq
-- for interactive use
readseq my.1st.seq my.2nd.seq -all -format=genbank -output=my.gb
-- convert all of two input files to one genbank format output file
readseq my.seq -all -form=pretty -nameleft=3 -numleft -numright -numtop -match
-- output to standard output a file in a pretty format
readseq my.seq -item=9,8,3,2 -degap -CASE -rev -f=msf -out=my.rev
-- select 4 items from input, degap, reverse, and uppercase them
cat *.seq | readseq -pipe -all -format=asn > bunch-of.asn
-- pipe a bunch of data thru readseq, converting all to asn
The brief usage of readseq is as follows. The "[]" denote
optional parts of the syntax:
readseq -help
readSeq (27Dec92), multi-format molbio sequence reader.
usage: readseq [-options] in.seq > out.seq
options
-a[ll] select All sequences
-c[aselower] change to lower case
-C[ASEUPPER] change to UPPER CASE
-degap[=-] remove gap symbols
-i[tem=2,3,4] select Item number(s) from several
-l[ist] List sequences only
-o[utput=]out.seq redirect Output
-p[ipe] Pipe (command line, <stdin, >stdout)
-r[everse] change to Reverse-complement
-v[erbose] Verbose progress
-f[ormat=]# Format number for output, or
-f[ormat=]Name Format name for output:
1. IG/Stanford 10. Olsen (in-only)
2. GenBank/GB 11. Phylip3.2
3. NBRF 12. Phylip
4. EMBL 13. Plain/Raw
5. GCG 14. PIR/CODATA
6. DNAStrider 15. MSF
7. Fitch 16. ASN.1
8. Pearson/Fasta 17. PAUP
9. Zuker 18. Pretty (out-only)
Pretty format options:
-wid[th]=# sequence line width
-tab=# left indent
-col[space]=# column space within sequence line on output
-gap[count] count gap chars in sequence numbers
-nameleft, -nameright[=#] name on left/right side [=max width]
-nametop name at top/bottom
-numleft, -numright seq index on left/right side
-numtop, -numbot index on top/bottom
-match[=.] use match base for 2..n species
-inter[line=#] blank line(s) between sequence blocks
Recent changes:
4 May 92
+ added 32 bit CRC checksum as alternative to GCG 6.5bit checksum
Aug 92
= fixed Olsen format input to handle files w/ more sequences,
not to mess up when more than one seq has same identifier,
and to convert number masks to symbols.
= IG format fix to understand ^L
30 Dec 92
* revised command-line & interactive interface. Suggested form is now
readseq infile -format=genbank -output=outfile -item=1,3,4 ...
but remains compatible with prior commandlines:
readseq infile -f2 -ooutfile -i3 ...
+ added GCG MSF multi sequence file format
+ added PIR/CODATA format
+ added NCBI ASN.1 sequence file format
+ added Pretty, multi sequence pretty output (only)
+ added PAUP multi seq format
+ added degap option
+ added Gary Williams (GWW, G.Williams@CRC.AC.UK) reverse-complement option.
+ added support for reading Phylip formats (interleave & sequential)
* string fixes, dropped need for compiler flags NOSTR, FIXTOUPPER, NEEDSTRCASECMP
* changed 32bit checksum to default, -DSMALLCHECKSUM for GCG version
1Feb93
= reverted Genbank output format to fixed left margin
(change in 30 Dec release), so GDE and others relying on fixed margin
can read this.

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* ReadSeq.Help -- 30 Dec 92
*
* Reads and writes nucleic/protein sequences in various
* formats. Data files may have multiple sequences.
*
* Copyright 1990 by d.g.gilbert
* biology dept., indiana university, bloomington, in 47405
* e-mail: gilbertd@bio.indiana.edu
*
* This program may be freely copied and used by anyone.
* Developers are encourged to incorporate parts in their
* programs, rather than devise their own private sequence
* format.
*
* This should compile and run with any ANSI C compiler.
* Please advise me of any bugs, additions or corrections.
Readseq is particularly useful as it automatically detects many
sequence formats, and interconverts among them.
Formats which readseq currently understands:
* IG/Stanford, used by Intelligenetics and others
* GenBank/GB, genbank flatfile format
* NBRF format
* EMBL, EMBL flatfile format
* GCG, single sequence format of GCG software
* DNAStrider, for common Mac program
* Fitch format, limited use
* Pearson/Fasta, a common format used by Fasta programs and others
* Zuker format, limited use. Input only.
* Olsen, format printed by Olsen VMS sequence editor. Input only.
* Phylip3.2, sequential format for Phylip programs
* Phylip, interleaved format for Phylip programs (v3.3, v3.4)
* Plain/Raw, sequence data only (no name, document, numbering)
+ MSF multi sequence format used by GCG software
+ PAUP's multiple sequence (NEXUS) format
+ PIR/CODATA format used by PIR
+ ASN.1 format used by NCBI
+ Pretty print with various options for nice looking output. Output only.
See the included "Formats" file for detail on file formats.
Example usage:
readseq
-- for interactive use
readseq my.1st.seq my.2nd.seq -all -format=genbank -output=my.gb
-- convert all of two input files to one genbank format output file
readseq my.seq -all -form=pretty -nameleft=3 -numleft -numright -numtop -match
-- output to standard output a file in a pretty format
readseq my.seq -item=9,8,3,2 -degap -CASE -rev -f=msf -out=my.rev
-- select 4 items from input, degap, reverse, and uppercase them
cat *.seq | readseq -pipe -all -format=asn > bunch-of.asn
-- pipe a bunch of data thru readseq, converting all to asn
The brief usage of readseq is as follows. The "[]" denote
optional parts of the syntax:
readseq -help
readSeq (27Dec92), multi-format molbio sequence reader.
usage: readseq [-options] in.seq > out.seq
options
-a[ll] select All sequences
-c[aselower] change to lower case
-C[ASEUPPER] change to UPPER CASE
-degap[=-] remove gap symbols
-i[tem=2,3,4] select Item number(s) from several
-l[ist] List sequences only
-o[utput=]out.seq redirect Output
-p[ipe] Pipe (command line, <stdin, >stdout)
-r[everse] change to Reverse-complement
-v[erbose] Verbose progress
-f[ormat=]# Format number for output, or
-f[ormat=]Name Format name for output:
1. IG/Stanford 10. Olsen (in-only)
2. GenBank/GB 11. Phylip3.2
3. NBRF 12. Phylip
4. EMBL 13. Plain/Raw
5. GCG 14. PIR/CODATA
6. DNAStrider 15. MSF
7. Fitch 16. ASN.1
8. Pearson/Fasta 17. PAUP
9. Zuker 18. Pretty (out-only)
Pretty format options:
-wid[th]=# sequence line width
-tab=# left indent
-col[space]=# column space within sequence line on output
-gap[count] count gap chars in sequence numbers
-nameleft, -nameright[=#] name on left/right side [=max width]
-nametop name at top/bottom
-numleft, -numright seq index on left/right side
-numtop, -numbot index on top/bottom
-match[=.] use match base for 2..n species
-inter[line=#] blank line(s) between sequence blocks
Notes:
In use, readseq will respond to command line arguments, or to
interactive use. Command line arguments cannot be combined
but must each follow a switch character (-). In this release,
the command line options are now words, with an equals (=)
to separate parameter(s) fromt he command. You cannot put a
space between a command and its parameter, as is usual for
Unix programs (this is to preserve compatibility with VMS).
The command line syntax of the earlier versions is still
supported.
See the file Formats for details of the sequence formats which
are supported by readseq. The auto-detection feature of
readseq which distinguishes these formats looks for some of the
unique keywords and symbols that are found in each format. It
is not infallible at this, though it attempts to exclude unknown
formats. In general, if you feed to readseq a sequence file that
you know is one of these common formats, you are okay. If you feed
it data that might be oddball formats, or non-sequence data,
you might well get garbage results. Also, different developers
are always thinking up minor twists on these common formats
(like PAUP requiring a blank line between blocks of Phylip format,
or IG adding form feeds between sequences), which may cause hassles.
In general, output supports only minimal subsets of each format
needed for sequence data exchanges. Features, descriptions
and other format-unique information is discarded.
The pretty format requires additional options to generate a
nice output. Try the various pretty options to see what you like.
Pretty format is OUPUT only, readseq cannot read a Pretty format
file.
Readseq is NOT optimized for LARGE files. It generally makes several
reads thru each input file (one per sequence output at present, future
version may optimize this). It should handle input and output files
and sequences of any size, but will slow down quite a bit for very large
(multi megabyte) sized files. It is NOT recommended for converting
databanks or large subsets there-of. It is primarily directed at the
small files that researchers use to maintain their personal data, which
they frequently need to interconvert for the various analysis programs
which so frequently require a special format.
Users of Olsen multi sequence editor (VMS). The Olsen format
here is produced with the print command:
print/out=some.file
Use Genbank output from readseq to produce a format that this
editor can read, and use the command
load/genbank some.file
Dan Davison has a VMS program that will convert to/from the
Olsen native binary data format. E-mail davison@uh.edu
Warning: Phylip format input is now supported (30Dec92), however the
auto-detection of Phylip format is very probabilistic and messy,
especially distinguishing sequential from interleaved versions. It
is not recommended that one use readseq to convert files from Phylip
format to others unless essential.
This program is available thru Internet gopher, as
gopher ftp.bio.indiana.edu
browse into the IUBio-Software+Data/molbio/readseq/ folder
select the readseq.shar document
Or thru anonymous FTP in this manner:
my_computer> ftp ftp.bio.indiana.edu (or IP address 129.79.224.25)
username: anonymous
password: my_username@my_computer
ftp> cd molbio/readseq
ftp> get readseq.shar
ftp> bye
readseq.shar is a Unix shell archive of the readseq files.
This file can be editted by any text editor to reconstitute the
original files, for those who do not have a Unix system or an
Unshar program. Read the top of this .shar file for further
instructions.
There are also pre-compiled executables for the following computers:
Silicon Graphics Iris, Sparc (Sun Sparcstation & clones), VMS-Vax,
Macintosh. Use binary ftp to transfer these, except Macintosh. The
Mac version is just the command-line program in a window, not very
handy.
C source files:
readseq.c ureadseq.c ureadasn.c ureadseq.h
Document files:
Readme (this doc)
Formats (description of sequence file formats)
add.gdemenu (GDE program users can add this to the .GDEmenu file)
Stdfiles -- test sequence files
Makefile -- Unix make file
Make.com -- VMS make file
*.std -- files for testing validity of readseq
Recent changes (see also readseq.c for all history of changes):
4 May 92
+ added 32 bit CRC checksum as alternative to GCG 6.5bit checksum
Aug 92
= fixed Olsen format input to handle files w/ more sequences,
not to mess up when more than one seq has same identifier,
and to convert number masks to symbols.
= IG format fix to understand ^L
30 Dec 92
* revised command-line & interactive interface. Suggested form is now
readseq infile -format=genbank -output=outfile -item=1,3,4 ...
but remains compatible with prior commandlines:
readseq infile -f2 -ooutfile -i3 ...
+ added GCG MSF multi sequence file format
+ added PIR/CODATA format
+ added NCBI ASN.1 sequence file format
+ added Pretty, multi sequence pretty output (only)
+ added PAUP multi seq format
+ added degap option
+ added Gary Williams (GWW, G.Williams@CRC.AC.UK) reverse-complement option.
+ added support for reading Phylip formats (interleave & sequential)
* string fixes, dropped need for compiler flags NOSTR, FIXTOUPPER, NEEDSTRCASECMP
* changed 32bit checksum to default, -DSMALLCHECKSUM for GCG version

134
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/* Stdfiles
generate standard files to test readseq
*/
C
#include <stdio.h>
/* no sequence formats use chars > #126, ignore these */
main(void)
{
int c;
puts("> alphabet['!'..'~']");
for (c = '!'; c <= '~'; c++) putc(c,stdout);
putc('\n', stdout);
}
link -w -t MPST -c 'MPS ' c.o <20>
"{Libraries}"Interface.o "{Libraries}"ToolLibs.o <20>
"{Libraries}"Runtime.o "{CLibraries}"StdClib.o
link.out > alphabet.orig
C
#include <stdio.h>
main(void)
{
/* note: symbols "*" and "/" removed as terminators for various formats */
const char *aminos = "ABCDEFGHIKLMNPQRSTVWXYZ";
const char *primenuc = "ACGTU";
const char *allsymbols = "_.-?<>{}[]()!@#$%^&=+;:'|`~\"\\";
char *c, all[256];
int count;
strcpy(all, aminos);
strcat(all, primenuc);
strcat(all, allsymbols);
puts("> nucleic/amino test");
for (count=0; count<4; count++) {
for (c = all; *c!=0; c++) putc(*c, stdout);
putc('\n', stdout);
}
}
link -w -t MPST -c 'MPS ' c.o <20>
"{Libraries}"Interface.o "{Libraries}"ToolLibs.o <20>
"{Libraries}"Runtime.o "{CLibraries}"StdClib.o
link.out > nucleic.std
#--------------------------
#standards (ship w/ readseq)
#note: not all alphabet.orig chars are expected to be passed by
# readseq. Numbers are dropped.
readseq -p alphabet.orig > alphabet.std
readseq -p -C alphabet.std > upper.std
cat alphabet.orig
> alphabet['!'..'~']
!"#$%&'()*+,-./0123456789:;<=>?@ABCDEFGHIJKLMNOPQRSTUVWXYZ[\]^_`abcdefghijklmnopqrstuvwxyz{|}~
cat alphabet.std
>alphabet['!'..'~'], 83 bases, 9429 checksum.
!"#$%&'()*+-./:;<=>?@ABCDEFGHIJKLMNOPQRSTUVWXYZ[\]
^_`abcdefghijklmnopqrstuvwxyz{|}~
cat upper.std
>alphabet['!'..'~'], 83 bases, 9429 checksum.
!"#$%&'()*+-./:;<=>?@ABCDEFGHIJKLMNOPQRSTUVWXYZ[\]
^_`ABCDEFGHIJKLMNOPQRSTUVWXYZ{|}~
cat nucleic.std
> nucleic/amino test
ABCDEFGHIKLMNPQRSTVWXYZACGTU_.-?<>{}[]()!@#$%^&=+;:'|`~"\
ABCDEFGHIKLMNPQRSTVWXYZACGTU_.-?<>{}[]()!@#$%^&=+;:'|`~"\
ABCDEFGHIKLMNPQRSTVWXYZACGTU_.-?<>{}[]()!@#$%^&=+;:'|`~"\
ABCDEFGHIKLMNPQRSTVWXYZACGTU_.-?<>{}[]()!@#$%^&=+;:'|`~"\
readseq -p nucleic.std
>nucleic/amino test, 228 bases, 5952 checksum.
ABCDEFGHIKLMNPQRSTVWXYZACGTU_.-?<>{}[]()!@#$%^&=+;
:'|`~"\ABCDEFGHIKLMNPQRSTVWXYZACGTU_.-?<>{}[]()!@#
$%^&=+;:'|`~"\ABCDEFGHIKLMNPQRSTVWXYZACGTU_.-?<>{}
[]()!@#$%^&=+;:'|`~"\ABCDEFGHIKLMNPQRSTVWXYZACGTU_
.-?<>{}[]()!@#$%^&=+;:'|`~"\
#----------------------------------
#test for general read/write of all chars:
readseq -p alphabet.std -otest.alpha
diff test.alpha alphabet.std
#test for valid toupper, general read/write:
readseq -p -C alphabet.std -otest.upper
diff test.upper upper.std
#for vms, use "-C" to preserve case
# readseq -p "-C" alphabet.std -otest.upper
#test for multiple sequence file conversions
# leave out gcg, raw;
# test of long seq conversion ?
# test of mail-header seq conversion ?
#test for valid format conversions
readseq -v -p -f1 nucleic.std -otest.f1
readseq -v -p -f2 test.f1 -otest.f2
readseq -v -p -f3 test.f2 -otest.f3
readseq -v -p -f4 test.f3 -otest.f4
readseq -v -p -f5 test.f4 -otest.f5
readseq -v -p -f6 test.f5 -otest.f6
readseq -v -p -f7 test.f6 -otest.f7
readseq -v -p -f8 test.f7 -otest.f8
readseq -v -p -f1 test.f8 -otest.f1b
diff test.f1 test.f1b
compare test.f1 test.f1b
readseq -v -p -f13 test.f8 -otest.f13 # raw, drops name
readseq -v -p -f9 test.f8 -otest.f9 # zuker, little used
#readseq -v -p -f10 test.f9 -otest.f10 # olsen, input only (output=raw)
readseq -v -p -f11 test.f8 -otest.f11 # phylip 3.2, output only
readseq -v -p -f12 test.f8 -otest.f12 # phylip 3.3, output only
readseq -v -p -f14 test.f8 -otest.f14 # phylip 3.4, output only
#clean up
rm test.<2E>
#-----------------------------
# some general tests
readseq -h
readseq

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#
# dgg added new readseq formats, 29 dec 92
#
item:Export Foreign Format
itemmethod:readseq in1 -pipe -all -form=$FORMAT > $OUTPUTFILE
itemhelp:readseq.help
arg:FORMAT
argtype:choice_menu
argchoice:GenBank:genbank
argchoice:IG/Stanford:ig
argchoice:NBRF:nbrf
argchoice:EMBL:embl
argchoice:GCG:gcg
argchoice:DNA Strider:strider
argchoice:Fitch:fitch
argchoice:Pearson/Fasta:pearson
argchoice:Zuker:zuker
argchoice:Olsen:olsen
argchoice:Phylip:phylip
#argchoice:Phylip v3.2:phylip3.2
argchoice:Plain text:raw
argchoice:ASN.1:asn
argchoice:PIR:pir
argchoice:MSF:msf
argchoice:PAUP:paup
argchoice:Pretty:pretty -nametop -nameleft=3 -numright -nameright -numtop
arg:OUTPUTFILE
argtype:text
arglabel:Save as?
in:in1
informat:genbank
#
#dgg addition for new readseq, 24 dec 92
#
item:Pretty Print
itemmethod:readseq in1 -p -a -f=pretty $NAMELEFT $NAMERIGHT $NUMTOP $NUMBOT $NUMLEFT $NUMRIGHT -col=$COLS -width=$WIDTH $MATCH $GAPC > in1.pretty; (textedit in1.pretty; /bin/rm -f in1 in1.pretty)&
itemhelp:readseq.help
#nametop is bad !?
in:in1
informat:genbank
arg:NAMETOP
argtype:chooser
arglabel:Names at top ?
argchoice:No:
argchoice:Yes:-nametop
arg:NAMELEFT
argtype:chooser
arglabel:Names at left ?
argchoice:No:
argchoice:Yes:-nameleft
arg:NAMERIGHT
argtype:chooser
arglabel:Names at right?
argchoice:Yes:-nameright
argchoice:No:
arg:NUMTOP
argtype:chooser
arglabel:Numbers at top ?
argchoice:Yes:-numtop
argchoice:No:
arg:NUMBOT
argtype:chooser
arglabel:Numbers at tail ?
argchoice:No:
argchoice:Yes:-numbot
arg:NUMLEFT
argtype:chooser
arglabel:Numbers at left ?
argchoice:Yes:-numleft
argchoice:No:
arg:NUMRIGHT
argtype:chooser
arglabel:Numbers at right?
argchoice:Yes:-numright
argchoice:No:
arg:MATCH
argtype:chooser
arglabel:Use match '.' for 2..n species?
argchoice:No:
argchoice:Yes:-match
arg:GAPC
argtype:chooser
arglabel:Count gap symbols?
argchoice:No:
argchoice:Yes:-gap
arg:WIDTH
argtype:slider
arglabel:Sequence width?
argmin:10
argmax:200
argvalue:50
arg:COLS
argtype:slider
arglabel:Column spacers?
argmin:0
argmax:50
argvalue:10
### pretty print insert end
#

412
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/*------------------------------------------------------------------------------
#
#
# MultiFinder-Aware Simple Input/Output Window resource
#
# for ReadSeq
#
------------------------------------------------------------------------------*/
#include "systypes.r"
#include "types.r"
resource 'MENU' (20000, preload) {
20000,
textMenuProc,
0x7FFFFFFD,
enabled,
apple,
{ /* array: 2 elements */
/* [1] */
"About ReadSeq<65>", noIcon, noKey, noMark, plain,
/* [2] */
"-", noIcon, noKey, noMark, plain
}
};
resource 'MENU' (20001, preload) {
20001,
textMenuProc,
0x0,
enabled,
"File",
{ /* array: 11 elements */
/* [1] */
"New", noIcon, "N", noMark, plain,
/* [2] */
"Open", noIcon, "O", noMark, plain,
/* [3] */
"-", noIcon, noKey, noMark, plain,
/* [4] */
"Close", noIcon, "W", noMark, plain,
/* [5] */
"Save", noIcon, "S", noMark, plain,
/* [6] */
"Save As<41>", noIcon, noKey, noMark, plain,
/* [7] */
"-", noIcon, noKey, noMark, plain,
/* [8] */
"Page Setup<75>", noIcon, noKey, noMark, plain,
/* [9] */
"Print<EFBFBD>", noIcon, noKey, noMark, plain,
/* [10] */
"-", noIcon, noKey, noMark, plain,
/* [11] */
"Quit", noIcon, "Q", noMark, plain
}
};
resource 'MENU' (20002, preload) {
20002,
textMenuProc,
0x0,
enabled,
"Edit",
{ /* array: 6 elements */
/* [1] */
"Undo", noIcon, "Z", noMark, plain,
/* [2] */
"-", noIcon, noKey, noMark, plain,
/* [3] */
"Cut", noIcon, "X", noMark, plain,
/* [4] */
"Copy", noIcon, "C", noMark, plain,
/* [5] */
"Paste", noIcon, "V", noMark, plain,
/* [6] */
"Clear", noIcon, noKey, noMark, plain
}
};
resource 'MENU' (20003, preload) {
20003,
textMenuProc,
allEnabled,
enabled,
"Font",
{ /* array: 0 elements */
}
};
resource 'ALRT' (20000, purgeable) {
{98, 108, 314, 405},
20000,
{ /* array: 4 elements */
/* [1] */
OK, visible, silent,
/* [2] */
OK, visible, silent,
/* [3] */
OK, visible, silent,
/* [4] */
OK, visible, silent
}
};
resource 'ALRT' (20001, purgeable) {
{40, 20, 150, 260},
20001,
{ /* array: 4 elements */
/* [1] */
OK, visible, silent,
/* [2] */
OK, visible, silent,
/* [3] */
OK, visible, silent,
/* [4] */
OK, visible, silent
}
};
resource 'ALRT' (20002, preload) {
{72, 64, 212, 372},
20002,
{ /* array: 4 elements */
/* [1] */
OK, visible, silent,
/* [2] */
OK, visible, silent,
/* [3] */
OK, visible, silent,
/* [4] */
OK, visible, silent
}
};
resource 'DITL' (20000, purgeable) {
{ /* array DITLarray: 8 elements */
/* [1] */
{191, 98, 211, 178},
Button {
enabled,
"OK"
},
/* [2] */
{110, 24, 130, 256},
StaticText {
disabled,
" Copyright <20> 1990 by d.g.gilbert\n"
},
/* [3] */
{6, 93, 24, 281},
StaticText {
disabled,
"A tool for molecular biology."
},
/* [4] */
{31, 25, 86, 281},
StaticText {
disabled,
"Reads and writes nucleic or protein sequ"
"ences in various formats. Data files may"
" have multiple sequences."
},
/* [5] */
{6, 17, 22, 92},
StaticText {
disabled,
"ReadSeq"
},
/* [6] */
{150, 28, 186, 262},
StaticText {
disabled,
"land mail: biology dept., indiana univer"
"sity, bloomington, in 47405\n"
},
/* [7] */
{129, 25, 153, 258},
StaticText {
disabled,
" e-mail: gilbertd@bio.indiana.edu\n"
},
/* [8] */
{86, 12, 107, 281},
StaticText {
disabled,
"This program may be freely distributed."
}
}
};
resource 'DITL' (20001, purgeable) {
{ /* array DITLarray: 3 elements */
/* [1] */
{80, 150, 100, 230},
Button {
enabled,
"OK"
},
/* [2] */
{10, 60, 60, 230},
StaticText {
disabled,
"Error. ^0."
},
/* [3] */
{8, 8, 40, 40},
Icon {
disabled,
2
}
}
};
resource 'DITL' (20002, preload) {
{ /* array DITLarray: 4 elements */
/* [1] */
{58, 25, 76, 99},
Button {
enabled,
"Yes"
},
/* [2] */
{86, 25, 104, 99},
Button {
enabled,
"No"
},
/* [3] */
{12, 20, 45, 277},
StaticText {
disabled,
"Save changes before closing?"
},
/* [4] */
{86, 195, 104, 269},
Button {
enabled,
"Cancel"
}
}
};
resource 'CNTL' (20000, purgeable, preload) {
{-1, 465, 272, 481},
0,
invisible,
0,
0,
scrollBarProc,
0,
""
};
resource 'CNTL' (20001, purgeable, preload) {
{271, -1, 287, 466},
0,
invisible,
0,
0,
scrollBarProc,
0,
""
};
data 'pzza' (128, purgeable) {
$"4D50 5320" /* MPS */
};
resource 'MBAR' (20000, preload) {
{ /* array MenuArray: 4 elements */
/* [1] */
20000,
/* [2] */
20001,
/* [3] */
20002,
/* [4] */
20003
}
};
resource 'WIND' (20000, purgeable, preload) {
{0, 0, 286, 480},
zoomDocProc,
invisible,
noGoAway,
0x0,
"untitled"
};
resource 'STR#' (20000, purgeable) {
{ /* array StringArray: 11 elements */
/* [1] */
"You must run on 512Ke or later",
/* [2] */
"Application Memory Size is too small",
/* [3] */
"Not enough memory to run SIOW",
/* [4] */
"Not enough memory to do Cut",
/* [5] */
"Cannot do Cut",
/* [6] */
"Cannot do Copy",
/* [7] */
"Cannot exceed 32,000 characters with Pas"
"te",
/* [8] */
"Not enough memory to do Paste",
/* [9] */
"Cannot create window",
/* [10] */
"Cannot exceed 32,000 characters",
/* [11] */
"Cannot do PasteFont not found"
}
};
resource 'SIZE' (-1) {
reserved,
acceptSuspendResumeEvents,
reserved,
canBackground,
multiFinderAware,
backgroundAndForeground,
dontGetFrontClicks,
ignoreChildDiedEvents,
not32BitCompatible,
notHighLevelEventAware,
onlyLocalHLEvents,
notStationeryAware,
dontUseTextEditServices,
reserved,
reserved,
reserved,
124928,
38912
};
resource 'SIZE' (0) {
reserved,
acceptSuspendResumeEvents,
reserved,
canBackground,
multiFinderAware,
backgroundAndForeground,
dontGetFrontClicks,
ignoreChildDiedEvents,
not32BitCompatible,
notHighLevelEventAware,
onlyLocalHLEvents,
notStationeryAware,
dontUseTextEditServices,
reserved,
reserved,
reserved,
256000,
38912
};
data 'siow' (0) {
$"0F52 6561 6453 6571 2069 6E20 5349 4F57" /* .ReadSeq in SIOW */
};
resource 'BNDL' (128) {
'siow',
0,
{ /* array TypeArray: 2 elements */
/* [1] */
'ICN#',
{ /* array IDArray: 1 elements */
/* [1] */
0, 128
},
/* [2] */
'FREF',
{ /* array IDArray: 1 elements */
/* [1] */
0, 128
}
}
};
resource 'FREF' (128) {
'APPL',
0,
""
};
resource 'ICN#' (128) {
{ /* array: 2 elements */
/* [1] */
$"0000 0000 0000 0000 0010 4100 0010 2200"
$"0020 2200 0020 2100 0020 4100 0010 4200"
$"0010 4200 0010 2200 0020 2100 0020 0100"
$"00FF FF00 03FF FFE0 0791 03F0 0ED1 0E7C"
$"1C31 321C 380D C10E 3FFF FFFE 3003 C106"
$"380D 300E 1E31 0E3C 1FC1 01F8 07FF FFE0"
$"00FF FE",
/* [2] */
$"0000 0000 0000 0000 0010 4100 0010 2200"
$"0020 2200 0020 2100 0020 4100 0010 4200"
$"0010 4200 0010 2200 0020 2100 0020 0100"
$"00FF FF00 03FF FFE0 07FF FFF0 0FFF FFFC"
$"1FFF FFFC 3FFF FFFE 3FFF FFFE 3FFF FFFE"
$"3FFF FFFE 1FFF FFFC 1FFF FFF8 07FF FFE0"
$"00FF FE"
}
};

42
readseqSIOW.make Normal file
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# Macintosh MPW-C Makefile
# using Simple Input/Output Window library
#
# File: ReadseqSIOW.make
# Target: ReadseqSIOW
# Sources: readseq.c ureadseq.c ureadasn.c macinit.c
# Created: Wednesday, November 13, 1991 8:23:00 PM
#OBJECTS = macinit.c.o readseq.c.o ureadseq.c.o
#COptions = -D SIOW # -r
#if NCBI is available, set path here to NCBI toolkit:
NCBI = "{Boot}@molbio:ncbi:"
OBJECTS = macinit.c.o readseq.c.o ureadseq.c.o ureadasn.c.o
COptions = -D SIOW -d NCBI -i "{NCBI}"include:
NCBILIBS = "{NCBI}"lib:libncbi.o "{NCBI}"lib:libncbiobj.o "{NCBI}"lib:libvibrant.o
#endif NCBI
ReadseqSIOW <20><> ReadseqSIOW.make {OBJECTS}
Link -d -c '????' -t APPL <20>
{OBJECTS} <20>
"{CLibraries}"StdClib.o <20>
"{MPW}"Libraries:Libraries:SIOW.o <20>
"{Libraries}"Runtime.o <20>
"{Libraries}"Interface.o <20>
#if NCBI
{NCBILIBS} <20>
"{CLibraries}"CSANELib.o <20>
"{CLibraries}"Math.o <20>
#endif NCBI
-o ReadseqSIOW
readseq.c.o <20> ReadseqSIOW.make readseq.c
ureadseq.c.o <20> ReadseqSIOW.make ureadseq.c
macinit.c.o <20> ReadseqSIOW.make macinit.c
#if NCBI
ureadasn.c.o <20> ReadseqSIOW.make ureadasn.c
#endif NCBI
ReadseqSIOW <20><> macinit.r
Rez -a macinit.r -o ReadseqSIOW