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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 ob-
     jects.

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/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				   2016-09-01			     CLEANASN(1)

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