NAME

tbl2asn - prepare a GenBank submission using an ASCII feature table

SYNOPSIS

tbl2asn [-] [-A str] [-C str] [-D filename] [-E] [-F str] [-G str] [-H str] [-J] [-K] [-L] [-M str] [-N n] [-O] [-P] [-Q str] [-R] [-S] [-T] [-U] [-V str] [-W] [-X str] [-Y filename] [-Z filename] [-a str] [-b] [-c str] [-f filename] [-g] [-h] [-i filename] [-j str] [-k str] [-l str] [-m str] [-n str] [-o filename] [-p str] [-q] [-r str] [-s] [-t filename] [-u] [-v] [-w filename] [-x str] [-y str] [-z]

DESCRIPTION

tbl2asn reads a template along with sequence and table files, and outputs ASN.1 for submission to GenBank. Thus, the submitter does not need to read each set of table and sequence files into Sequin. Furthermore, the template file can contain the organism and submitter information common to all records, obviating the need to input these data for each sequence/table pair.

OPTIONS

A summary of options is included below.

-: Print usage message
-a str: Accession
-C str: Genome Center tag
-D filename: Descriptors file
-E: Recurse
-F: Feature ID links:

o: By Overlap
p: By Product
l: By Label and Location
s: Suppress links forced by -M

-G str: Alignment Gap Flags (comma separated fields, e.g., p,-,-,-,?,. ) n Nucleotide or p Protein, Begin, Middle, End Gap Characters, Missing Characters, Match Characters Alignment middle Gap characters
-H str: Hold until publication:

y: For one year
mm/dd/yyyy: Until the specified date

-J: Delayed genomic product set
-K: Safe Bioseq-set
-L: Force Local protein_id/transcript_id
-M str: Master genome flags:

n: Normal
b: Big sequence
p: Power option
t: TSA

-N n: Project version number
-O: Allow run-on ORFs
-P: Remote publication lookup
-Q: mRNA title policy

s: Special mRNA titles
r: RefSeq mRNA titles

-R: Remote sequence record fetching from ID
-S: Smart feature annotation
-T: Remote Taxonomy lookup
-U: Remove Unnecessary gene xref
-V str: Verification (combine any of the following letters)

v: Validate with Normal Stringency
r: Validate without Country Check
c: BarCode validation
b: Generate GenBank Flatfile
g: Generate Gene Report
t: Validate with TSA check

-W: Log progress
-X str: Extra flags (combine any of the following letters)

A: Automatic definition line generation
C: Apply Comments in .cmt files to all sequences
E: Treat like Eukarypota in the discrepancy report

-Y filename: Read a comment string from filename
-Z filename: Write a discrepancy report to filename
-a str: File type:

a: Any (default)
r20u: Runs of 20+ Ns are gaps, 100 Ns are unknown length
r20k: Runs of 20+ Ns are gaps, 100 Ns are known length
r10u: Runs of 10+ Ns are gaps, 100 Ns are unknown length
r10k: Runs of 10+ Ns are gaps, 100 Ns are known length
s: FASTA Set (s Batch, s1 Pop, s2 Phy, s3 Mut, s4 Eco, s9 Small-genome)
d: FASTA Delta
di: FASTA Delta with Implicit Gaps
l: FASTA+Gap Alignment (l Batch, l1 Pop, l2 Phy, l3 Mut, l4 Eco, l9 Small-genome)
z: FASTA with Gap Lines
e: PHRAP/ACE
b: ASN.1 (in conjunction with

-b: Generate GenBank file (deprecated in favor of -V b)
-c str: Cleanup (combine any of the following letters)

d: Correct Collection Dates (assume month first)
D: Correct Collection Dates (assume day first)
b: Append note to coding regions that overlap other coding regions with similar product names and do not contain 'ABC'
x: Extend partial ends of features by one or two nucleotides to abut gaps or sequence ends
p: Add exception to non-extendable partials
s: Add exception to short introns
f: Fix product names

-f filename: Single table file
-g: Input is a genomic product set
-h: Convert general ID to note
-i filename: Single input file
-j str: Source qualifiers
-k str: CDS flags (combine any of the following letters)

c: Annotate Longest ORF
r: Allow Runon ORFs
m: Allow Alternative Starts
k: Set Conflict on Mismatch

-l str: Add type of evidence used to assert linkage across assembly gaps (only for TSA records). Must be one of the following:

paired-ends
align-genus
align-xgenus
align-trnscpt
within-clone
clone-contig
map
strobe

-m str: Lineage to use for discrepancy report tests
-n str: Organism name
-o filename: Single output file
-p str: Path to files
-q: Set sequence ID from input file name
-r str: Path for results
-s: Read FASTAs as Set
-t filename: Read template from filename
-u: Convert GenProdSet to NucProtSet
-v: Validate (deprecated in favor of -V v)
-w filename: Single structured comment file (overrides the use of -X C)
-x str: Suffix (default = .fsa)
-y str
-z: Clean up log file Comment

AUTHOR

The National Center for Biotechnology Information.

NAME

SYNOPSIS

DESCRIPTION

OPTIONS

AUTHOR

SEE ALSO