Man page - correct_abundances(1)

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Manual

CORRECT_ABUNDANCES

NAME
SYNOPSIS
DESCRIPTION
OPTIONS

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 โ€™run_mappers.pyโ€™ and โ€™create_similarity_matrix.pyโ€™.

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]