NCBI C++ Toolkit Mar_17_2008 (Default branch)


 
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Old 04-18-2008
NCBI C++ Toolkit Mar_17_2008 (Default branch)

The NCBI C++ Toolkit provides portable librariesand applications for assisting genetic science.These include libraries for networking, SQL andBerkeleyDB access, CGI and HTML handling, ASN.1and XML handling, sequence alignment engines,sequence retrieval engines, BLAST databaseengines, FLTK and OpenGL graphics toolkits, andbasic system utilities.License: Public DomainChanges:
Extensive additions to all sections of the API. Assorted bugfixes.Image

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ASN2FF(1)						     NCBI Tools User's Manual							 ASN2FF(1)

NAME
asn2ff - convert ASN.1 biological data to a flat format (old version) SYNOPSIS
asn2ff [-] [-A X] [-B X] [-C] [-G] [-L F] [-M] [-R] [-V F] [-a filename] [-b] [-d] [-e] [-f b/p/e/s/x/z] [-g] [-h F] [-k F] [-l filename] [-m r/d/s/c/k/l/e/p] [-n F] [-o filename] [-p F] [-q] [-r filename] [-s] [-t] [-v F] [-w] [-y] [-z] DESCRIPTION
asn2ff converts descriptions of biological sequences from NCBI's ASN.1 format to one of several flat-file formats. This program is built around a deprecated interface; please use asn2gb(1) instead. OPTIONS
A summary of options is included below. - Print usage message -A X Show region starting at X (default is 0) -B X Show region ending at X (default is last position) -C Show Bankit comments -G Output is one top bioseq only in genome view -L F Use old (pre-Genbank 127.0) LOCUS line format -M Output is map bioseqs only -R For GenBank Release -V F Don't use VERSION -a filename Filename for ASN.1 input (default is stdin) -b Input asnfile in binary mode -d Use SeqMgr indexing -e Input is a Seq-entry -f b/p/e/s/x/z Output Format: b GenBank (default) p GenPept e EMBL s PseudoEMBL x GenBankSelect z EMBLPEPT -g Show gi numbers -h F Hide sequence -k F Don't use complex sets (phy-set,mut-set, pop-set) -l filename Log errors to filename -m r/d/s/c/k/l/e/p Output mode: r release (default) d dump s Sequin c Chromoscope k dir-sub-debug l dir-sub e revise p partial report -n F Strict gene_binding -o filename Output Filename (default is stdout) -p F Omit new gene features -q Output is one top bioseq only -r filename Output error logfile (default is stderr) -s Input is a Seq-submit -t Show verbose message text -v F Suppress error messages -w Use HTML output format -y Print help format only -z New algorithm for orgnames AUTHOR
The National Center for Biotechnology Information. SEE ALSO
asn2all(1), asn2asn(1), asn2fsa(1), asn2gb(1), asn2xml(1), asndhuff(1). NCBI
2005-05-16 ASN2FF(1)