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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] [-B str] [-C str] [-D	str] [-F str] [-K str]
       [-L filename]  [-M filename]  [-N str]  [-O 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

       -B str Branch, per the flags in str:
	      c	     Has coding	regions
	      d	     No	coding regions
	      p	     Passes validation
	      q	     Validator errors or rejects
	      r	     Only pop/phy/mut/eco/WGS sets
	      s	     Exclude pop/phy/mut/eco/WGS sets
	      t	     Only nuc-prot sets
	      u	     Exclude nuc-prot sets
	      v	     Only segmented sequences
	      w	     Exclude segmented sequences

       -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
	      t	     Non-NucProt segmented set to delta	sequence
	      u	     Improved non-NucProt segmented set	to delta sequence
	      g	     Raw to delta by assembly gap
	      m	     Merge assembly gap	features

       -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
	      a	     Title to name
	      b	     AutoDef title or name
	      x	     Prefix title with organism	name

       -F str Clean up features, per the flags in str:
	      u	     Remove User-objects
	      d	     Remove db_xrefs
	      e	     Remove /evidence and /inference
	      g	     Fuse multi-interval genes
	      i	     Fuse adjacent-interval imported features
	      r	     Remove redundant gene xrefs
	      f	     Fuse duplicate features
	      s	     Package features on referenced Bioseq
	      k	     Package coding-region or parts features
	      z	     Delete or update EC numbers
	      b	     Set Best coding-region reading frame
	      x	     Retranslate coding	regions
	      a	     Adjust for	missing	stop codon

       -K str Perform a	general	cleanup, per the flags in str:
	      b	     BasicSeqEntryCleanup
	      p	     C++ BasicCleanup (via an external utility)
	      v	     AdvancedSeqEntryCleanup
	      s	     SeriousSeqEntryCleanup
	      x	     ExtendedSeqEntryCleanup
	      g	     GpipeSeqEntryCleanup
	      n	     Normalize descriptor order
	      u	     Remove NcbiCleanup	User Objects
	      c	     Synchronize genetic Codes
	      f	     CDS partial from translation
	      e	     Impose CDS	partials
	      d	     Resynchronize CDS partials
	      m	     Resynchronize mRNA	partials
	      t	     Resynchronize Peptide partials
	      a	     Adjust consensus splice
	      i	     Promote to	"worst"	Seq-ID
	      r	     Reassign local IDs
	      l	     Remove locus

       -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
	      l	     Link CDS mRNA by Label and	Location
	      r	     Reassign feature IDs
	      m	     Merge colliding feature IDs
	      f	     Fix missing reciprocal feature IDs
	      c	     Clear feature IDs

       -O str Missing prot-ref name

       -P str Publication options:
	      a	     Remove All	publications
	      s	     Remove Serial number
	      f	     Remove Figure, numbering, and name
	      r	     Remove Remark
	      u	     Update PMID-only publication
	      j	     Lookup ISO	Journal	title abbreviation
	      m	     Merge identical publication features
	      #	     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
	      t	     tRNA anticodon report
	      w	     Component offset 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
	      s	     Automatic definition line with Source qualifiers
	      e	     Pop/Phy/Mut/Eco Set definition line
	      n	     Instantiate NC title
	      m	     Instantiate NM titles
	      x	     Special XM	titles
	      p	     Instantiate Protein titles
	      g	     GPipe instantiate titles
	      c	     Create mRNAs for coding sequences
	      f	     Fix reciprocal protein_id/transcript_id
	      v	     Revert preRNA or ncRNA transcript_id
	      t	     Parse anticodon from Sequence
	      b	     Batch cleanup of multireader output
	      z	     Wrap SegSet with NucProt set
	      w	     GFF/WGS genome cleanup

       -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 Bioseq-set
	      u	     Batch Seq-submit

       -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
	      i	     INSD
	      r	     RefSeq
	      n	     NCBI
	      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/ffd-
	      iff)

       -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				  2016-09-01			   CLEANASN(1)

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