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.