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cleanasn(1) [debian man page]

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

NAME
cleanasn - clean up irregularities in NCBI ASN.1 objects SYNOPSIS
cleanasn [-] [-A filename] [-C str] [-D str] [-F str] [-K str] [-L filename] [-M filename] [-N str] [-P str] [-Q str] [-R] [-S str] [-T] [-U str] [-V str] [-X str] [-Z str] [-a str] [-b] [-c] [-d str] [-f str] [-i filename] [-j filename] [-k filename] [-m str] [-n path] [-o filename] [-p path] [-q path] [-r path] [-v path] [-x ext] DESCRIPTION
cleanasn is a utility program to clean up irregularities in NCBI ASN.1 objects. OPTIONS
A summary of options is included below. - Print usage message -A filename Accession list file -C str Sequence operations, per the flags in str: c Compress d Decompress v Virtual gaps inside segmented sequence s Convert segmented set to delta sequence -D str Clean up descriptors, per the flags in str: t Remove Title c Remove Comment n Remove Nuc-Prot Set title e Remove Pop/Phy/Mut/Eco Set title m Remove mRNA title p Remove Protein title -F str Clean up features, per the flags in str: u Remove User-objects d Remove db_xrefs e Remove /evidence and /inference r Remove redundant gene xrefs f Fuse duplicate features k Package coding-region or parts features z Delete or update EC numbers -K str Perform a general cleanup, per the flags in str: b BasicSeqEntryCleanup p C++ BasicCleanup (via an external utility) s SeriousSeqEntryCleanup g GpipeSeqEntryCleanup n Normalize descriptor order u Remove NcbiCleanup User Objects c Synchronize genetic Codes d Resynchronize CDS partials m Resynchronize mRNA partials t Resynchronize Peptide partials a Adjust consensus splice i Promote to "worst" Seq-ID -L filename Log file -M filename Macro file -N str Clean up links, per the flags in str: o Link CDS mRNA by Overlap p Link CDS mRNA by Product r Reassign feature IDs f Fix missing reciprocal feature IDs c Clear feature IDs -P Publication options: a Remove All publications s Remove Serial number f Remove Figure, numbering, and name r Remove Remark u Update PMID-only publication # Replace unpublished with PMID -Q str Report: c Record count r ASN.1 BSEC report s ASN.1 SSEC report n NORM vs. SSEC report e PopPhyMutEco AutoDef report o Overlap report l Latitude-longitude country diff d Log SSEC differences g GenBank SSEC diff f asn2gb/asn2flat diff h Seg-to-delta GenBank diff v Validator SSEC diff m Modernize Gene/RNA/PCR u Unpublished Pub lookup p Published Pub lookup j Unindexed Journal report x Custom scan -R Remote fetching from ID (NCBI sequence databases) -S str Selective difference filter (capital letters skip) s SSEC b BSEC A Author p Publication l Location r RNA q Qualifier sort order g Genbank block k Package CdRegion or parts features m Move publication o Leave duplicate Bioseq publication d Automatic definition line e Pop/Phy/Mut/Eco Set definition line -T Taxonomy Lookup -U str Modernize, per the flags in str: g Genes r RNA p PCR Primers -V str Remove features by validator severity: r Reject e Error w Warning i Info -X str Miscellaneous options, per str: d Automatic definition line e Pop/Phy/Mut/Eco Set definition line n Instantiate NC title m Instantiate NM titles x Special XM titles p Instantiate Protein titles c Create mRNAs for coding sequences f Fix reciprocal protein_id/transcript_id -Z str Remove indicated User-object -a str ASN.1 type a Any (default) e Seq-entry b Bioseq s Bioseq-set m Seq-submit t Batch Processing [String] -b Input ASN.1 is Binary -c Input ASN.1 is Compressed -d str Source database a Any (default) g GenBank e EMBL d DDBJ b EMBL or DDBJ r RefSeq n NCBI v Only segmented sequences w Exclude segmented sequences x Exclude EMBL/DDBJ y Exclude gbcon, gbest, gbgss, gbhtg, gbpat, gbsts -f str Substring filter -i filename Single input file (defaults to stdin) -j filename First filename -k filename Last filename -m str Flatfile mode: r Release e Entrez s Sequin d Dump -n path asn2flat executable (default is /netopt/ncbi_tools/bin/asn2flat) -o filename Single output file (defaults to stdout) -p path Process all matching files in path -q path ffdiff executable (default is /netopt/genbank/subtool/bin/ffdiff) -r path Path for results -v path asnval executable (default is /netopt/ncbi_tools/bin/asnval) -x ext File selection suffix for use with -p (defaults to .ent) AUTHOR
The National Center for Biotechnology Information. SEE ALSO
asndisc(1), asnval(1), sequin(1). NCBI
2012-06-24 CLEANASN(1)
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