TBL2ASN(1)
π TBL2ASN(1) π the NCBI Tools User's Manual, but make it a group chat
hey bestie π«Ά you found the <hotpink>tbl2asn</hotpink> page, and honestly? iconic. this is the tool that turns your sequence + feature table situation into a real GenBank submission, and she does not need you hand-feeding every record into Sequin like it's 2004. strap in. π
β¨ NAME β¨
tbl2asn β prepare a GenBank submission using an ASCII feature table
no cap, that's the whole job description. π
πΈ SYNOPSIS πΈ
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]
look at all those little flags. she's giving alphabet soup π every single one of them is real and every single one of them is below.
π¦ DESCRIPTION π¦
okay so here's the tea, tbl2asn reads a template along with your sequence and table files, and outputs ASN.1 for submission to GenBank. that's it, that's the plot. β¨
and the reason this slaps? because you do not have to sit there and read each set of table and sequence files into Sequin one by one like some kind of Victorian orphan. π
and it gets better β the template file can hold the organism and submitter information that's common to all your records, so you're not re-typing the same data for every single sequence/table pair. she said "DRY principle" and she meant it. π
π₯ OPTIONS π₯
a summary of options is included below. (yes, all of them. we're doing this. hydrate first. π)
-β print usage message. that's it. a single lonely dash. she's mysterious, she's helpful.-a strβ Accession-C strβ Genome Center tag-D filenameβ Descriptors file-Eβ Recurse-Fβ Feature ID links:oβ By Overlappβ By Productlβ By Label and Locationsβ Suppress links forced by-M
-G strβ Alignment Gap Flags (comma separated fields, e.g.,p,-,-,-,?,.)nβ Nucleotide orpProtein, Begin, Middle, End Gap Characters, Missing Characters, Match Characters Alignment middle Gap characters
-H strβ Hold until publication:yβ For one yearmm/dd/yyyyβ Until the specified date
-Jβ Delayed genomic product set-Kβ Safe Bioseq-set-Lβ Force Localprotein_id/transcript_id-M strβ Master genome flags:nβ Normalbβ Big sequencepβ Power optiontβ TSA
-N nβ Project version number-Oβ Allow run-on ORFs-Pβ Remote publication lookup-Qβ mRNA title policysβ Special mRNA titlesrβ RefSeq mRNA titles
-Rβ Remote sequence record fetching from ID-Sβ Smart feature annotation-Tβ Remote Taxonomy lookup-Uβ Remove Unnecessary gene xref-V strβ Verification (combine any of the following letters)vβ Validate with Normal Stringencyrβ Validate without Country Checkcβ BarCode validationbβ Generate GenBank Flatfilegβ Generate Gene Reporttβ Validate with TSA check
-Wβ Log progress-X strβ Extra flags (combine any of the following letters)Aβ Automatic definition line generationCβ Apply Comments in.cmtfiles to all sequencesEβ Treat like Eukarypota in the discrepancy report
-Y filenameβ Read a comment string from filename-Z filenameβ Write a discrepancy report to filename-a strβ File type:aβ Any (default)r20uβ Runs of 20+ Ns are gaps, 100 Ns are unknown lengthr20kβ Runs of 20+ Ns are gaps, 100 Ns are known lengthr10uβ Runs of 10+ Ns are gaps, 100 Ns are unknown lengthr10kβ Runs of 10+ Ns are gaps, 100 Ns are known lengthsβ FASTA Set (sBatch,s1Pop,s2Phy,s3Mut,s4Eco,s9Small-genome)dβ FASTA Deltadiβ FASTA Delta with Implicit Gapslβ FASTA+Gap Alignment (lBatch,l1Pop,l2Phy,l3Mut,l4Eco,l9Small-genome)zβ FASTA with Gap Lineseβ PHRAP/ACEbβ ASN.1 (in conjunction withM)
-bβ Generate GenBank file (deprecated in favor of-V b)-c strβ Cleanup (combine any of the following letters)dβ Correct Collection Dates (assume month first)Dβ Correct Collection Dates (assume day first)bβ Append note to coding regions that overlap other coding regions with similar product names and do not contain'ABC'xβ Extend partial ends of features by one or two nucleotides to abut gaps or sequence endspβ Add exception to non-extendable partialssβ Add exception to short intronsfβ Fix product names
-f filenameβ Single table file-gβ Input is a genomic product set-hβ Convert general ID to note-i filenameβ Single input file-j strβ Source qualifiers-k strβ CDS flags (combine any of the following letters)cβ Annotate Longest ORFrβ Allow Runon ORFsmβ Allow Alternative Startskβ Set Conflict on Mismatch
-l strβ Add type of evidence used to assert linkage across assembly gaps (only for TSA records). Must be one of the following:paired-endsalign-genusalign-xgenusalign-trnscptwithin-cloneclone-contigmapstrobe
-m strβ Lineage to use for discrepancy report tests-n strβ Organism name-o filenameβ Single output file-p strβ Path to files-qβ Set sequence ID from input file name-r strβ Path for results-sβ Read FASTAs as Set-t filenameβ Read template from filename-uβ Convert GenProdSet to NucProtSet-vβ Validate (deprecated in favor of-V v)-w filenameβ Single structured comment file (overrides the use of-X C)-x strβ Suffix (default =.fsa)-y strβ no description given. she's a mystery, she's an enigma, she's giving main character energy with zero backstory. π-zβ Clean up log file Comment
heads up bestie: a couple of these are deprecated, and deprecated means "please use the new one instead" β-bwants you to use-V b, and-vwants you to use-V v. the old ones still show up to the party, but the cool kids moved on. π
π AUTHOR π
The National Center for Biotechnology Information.
(that's the whole author section. one line. she's concise, she's powerful, she ate. π)
β SEE ALSO β
Psequin(1)sbtedit(1)/usr/share/doc/ncbi-tools-bin/tbl2asn.txt.gz<http://www.ncbi.nlm.nih.gov/Sequin/table.html>
and that's the whole page, bestie π this one came to you straight from NCBI, dated 2016-09-01, and honestly she's still serving. now go submit something gorgeous. you've got this. π¦β¨
π¦ where this page comes from
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