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

NAME
asnval - validate ASN.1 biological sequence records SYNOPSIS
asnval [-] [-A] [-B] [-C N] [-D] [-E str] [-F] [-G] [-J] [-K] [-L filename] [-M] [-N flags] [-P N] [-Q N] [-R N] [-S N] [-T] [-U] [-X] [-Y] [-Z] [-a type] [-b] [-c] [-d path] [-e] [-f str] [-i filename] [-k] [-l] [-o filename] [-p path] [-q] [-r] [-u] [-v N] [-x str] DESCRIPTION
asnval is a command-line tool to validate ASN.1-format biological sequence records. OPTIONS
A summary of options is included below. - Print usage message -A Validate Alignments -B Validate Barcodes -C N Max count -D Disable message suppression -E str Only Error Code to Show -F Test network access -G GI lookup from accession -J Require ISO-JTA? -K Summary to error file -L filename Log File -M Match locus_tag against General ID -N flags Latitude-longitude / country flags 0 none 1 test state/province 2 ignore water exception 3 both of the above -P N Highest severity for error to show: 0 none 1 informational 2 warning 3 error (default for -Q) 4 grounds for rejection (default for -P, -R) -Q N Lowest severity for error to show, per P -R N Severity for error in return code, per P -S N Skip count -T Use Threads -U Genome center submission -X Exon splice check -Y Check against old IDs -Z Remote CDS product fetch -a type Input ASN.1 type: a Automatic (default) c Catenated z Any e seq-Entry b Bioseq s bioseq-Set m seq-subMit t baTch bioseq-set u batch seq-sUbmit -b Batch file is Binary -c Batch file is Compressed -d path Path to Indexed Binary ASN.1 Data -e Ignore transcription/translation Exceptions -x str Substring filter -i filename Single input file (standard input by default) -k Local fetching -l Lock components in advance -o filename Single output file -p path Path to ASN.1 Files -q Taxonomy lookup -r Remote Fetching from ID -u Recurse -v N Verbosity: 1 Standard report (default) 2 Accession / severity / code (space delimited) 3 Accession / severity / code (tab delimited) 4 XML report 5 Accession / GI / severity / code (tab delimited) -x str File selection substring (.ent by default) AUTHOR
The National Center for Biotechnology Information. SEE ALSO
asndisc(1), cleanasn(1), sequin(1). NCBI
2012-06-24 ASNVAL(1)

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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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