Provided by: anfo_0.98-9_amd64 bug

NAME

       anfo - find best alignment of short reads to database

SYNOPSIS

       anfo [ option | file ... ]

DESCRIPTION

       anfo aligns (short) sequencing reads to a (gigabase sized) database.  It uses a heuristic seeding method,
       but  then  applies  a  genuine  aligner  that allows gaps, understands damage patterns in ancient dna and
       produces an easy to interpret score.

       Input files can be any variety of FastA  or  FastQ  files,  or  a  native  anfo  binary  file,  optinally
       compressed  using  gziporbzip2.   The  file  format  is automatically recognized and other formats may be
       added.

OPTIONS

       -V, --version
              Print version number and exit.

       -o file, --output file
              Write output to file. file will be written in the native anfo binary format, which can be operated
              upon using anfo-tool or the bindings to guile.

       -c conffile, --config conffile
              Read configuration from conffile.  This file configures which indices are used, and  by  extension
              to  which  genomes  an alignment is made, what parameters to use in the aligner and can set paths.
              See the example file.

       -p num, --threads num
              Start num threads for alignment.  One such thread per processor core is usually best.

       -x num, --ixthreads num
              Start num threads for indexing.  Indexing normally uses less cpu power than  alignment,  so  fewer
              indexers than aligners is normally best.

       --solexa-scale
              When  reading  FastQ  files, use the Solexa scale (log-odds-ratios) instead of the standard Phread
              scale (probabilities).  If you use Solexa/Illumina sequencers, refer to your documentation whether
              you need this.  Else you don't.

       --fastq-origin ori
              Set origin for FastQ decoding to ori.  The standard and default is 33, but it must be  set  to  64
              for  some  versions of the Solexa/Illumina software.  If you use Solexa/Illumina sequencers, refer
              to your documentation whether you need this.  Else you don't.

       -q, --quiet
              Suppress all output except fatal errors.

       -v, --verbose
              Print a progress indicator during operation.

ENVIRONMENT

       ANFO_PATH
              Colon separated list of directories searched for genome and index files.

FILES

       /etc/popt
              The system wide configuration file for popt(3).  anfo identifies itself as "anfo" to popt.

       ~/.popt
              Per user configuration file for popt(3).

       /usr/share/doc/anfo/example/*.cfg
              Example configuration files to be used with anfo.

BUGS

       None known.

AUTHOR

       Udo Stenzel <udo_stenzel@eva.mpg.de>

SEE ALSO

       http://bioinf.eva.mpg.de/anfo

       anfo-tool(1), anfo-sge(1), fa2dna(1), dnaindex(1), popt(3), fasta(5)

Applications                                      OCTOBER 2009                                           ANFO(1)