NAME

       correct_abundances - run the genome abundance similarity correction step

SYNOPSIS

       correct_abundances NAMES

DESCRIPTION

       Run the similarity correction step.

       Note:  Although  it  is  possible  to  run  the  read  mappers by hand or to create the similarity matrix
       manually,  we  strongly  recommend  to   use   the   provided   Python   scripts   'run_mappers.py'   and
       'create_similarity_matrix.py'.

OPTIONS

       NAMES: Filename  of  the names file; the plain text names file should contain one name per line. The name
              is used as identifier in the whole algorithm.

       -h, --help
              show this help message and exit

       -m SMAT, --similarity-matrix=SMAT
              Path to similarity matrix file. The similarity matrix must be created with the  same  NAMES  file.
              [default: ./similarity_matrix.npy]

       -s SAM, --samfiles=SAM
              Pattern  pointing  to  the  SAM  files  created  by  the mapper. Placeholder for the name is "%s".
              [default: ./SAM/%s.sam]

       -b BOOT, --bootstrap-samples=BOOT
              Set the number of bootstrap samples. Use 1 to disable bootstrapping [default: 100]

       -o OUT, --output=OUT
              Plain text output file containing the results.  [default: ./results.txt]