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
- x
-
Only segmented proteins
- y
-
Exclude segmented proteins
- -C str
-
Sequence operations, per the flags in str:
- c
-
Compress
- d
-
Decompress
- l
-
Recalculated segmented sequence length
- 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.