tbl2asn(1) 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] [-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)
-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 ix 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
-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
-x str
Suffix (default = .fsa)
-y str
-z
Clean up log file Comment

AUTHOR

The National Center for Biotechnology Information.