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NAME

       Psequin - submit sequences to Genbank, EMBL, and DDBJ

SYNOPSIS

       Psequin  [-b]  [-bse] [-e] [-f filename] [-gc] [-h] [-oldaln] [-oldasn]
       [-oldgph] [-oldseq] [-oldsource] [-s] [-w] [-x]

DESCRIPTION

       Psequin is a program designed to aid in the submission of sequences  to
       the  GenBank,  EMBL, and DDBJ sequence databases. It was written at the
       National Center for Biotechnology Information,  part  of  the  National
       Library of Medicine at the National Institutes of Health.

       Psequin  can  assemble  the essential elements of a GenBank record from
       simple FASTA-format text files. For example, the  program  obtains  the
       proper genetic code from an organism name, and automatically determines
       coding region intervals by back-translation from the protein  sequence.
       An  on-line  help  window  scrolls to the appropriate place as the user
       moves between and within data entry forms, giving relevant  details  on
       what information is expected.

       Psequin  also  contains  a  number of built-in validation functions for
       quality assurance. Features such as  splice  sites  and  coding  region
       translations  are checked for accuracy or internal consistency. Double-
       clicking on an error message launches an appropriate  editor  by  which
       the user can correct any problems.

       Psequin  provides  live,  clickable  views  of the data in a variety of
       formats, including a report form, GenBank flatfile, EMBL flatfile,  and
       a  graphical  view.  Double clicking on an item in any of these formats
       launches an editor for that item. The editor is capable of  maintaining
       correct  feature  table positions as the underlying sequence is edited.
       It can display features on the  sequence  during  editing,  and  allows
       feature intervals to be adjusted by direct manipulation.

OPTIONS

       -b     Bioseq-set mode

       -bse   binseqentry mode

       -e     Entrez mode

       -f filename
              read from filename

       -gc    genome center mode

       -h     turn off automatic help

       -oldaln
              use old alignment reader

       -oldasn
              leave as old ASN.1

       -oldgph
              use old graphic view

       -oldseq
              use old sequence view

       -oldsource
              use old flat-file source format

       -s     subtool mode

       -w     workbench mode

       -x     read from standard input

AUTHOR

       The National Center for Biotechnology Information.

SEE ALSO

       sbtedit(1), tbl2asn(1), /usr/share/doc/ncbi-tools-x11/sequin.htm,
       <http://www.ncbi.nlm.nih.gov/Sequin/>.