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TBL2ASN(1)		    NCBI Tools User's Manual		      TBL2ASN(1)

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 M.PD
     -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 re-
		   gions 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.

SEE ALSO
     Psequin(1), sbtedit(1), tbl2asn.txt, <http://www.ncbi.nlm.nih.gov/Se-
     quin/table.html>.

NCBI				   2016-09-01			      TBL2ASN(1)

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