qualityScores(1)
toolkit for processing next-gen sequencing data
Description
QUALITYSCORES
NAME
qualityScores - toolkit for processing next-gen sequencing data
DESCRIPTION
qualityScore Version 2.0.1
Retrieve Phred score for read bases
Usage:
./qualityScores [options] -i <input_file> -o <output_file>
Required
arguments:
-i <string>
Name of input file including read data. The default format is Fastq.
-o <string>
Name of output file that is a text file including Phred scores for each read base.
Optional arguments:
|
--gzFASTQinput Input file is in gzipped Fastq format. |
--BAMinput
Input file is in BAM format.
--SAMinput
Input file is in SAM format.
--first-end
Use only first reads in paired-end data. Only applicable for paired-end BAM/SAM input.
--second-end
Use only second reads in paired-end data. Only applicable for paired-end BAM/SAM input.
|
--counted-reads <int> Total number of reads to be extracted from the input |
file. 10,000 by default.
|
--phred-offset <33|64> refer to subread aligner. |
AUTHOR
This manpage was
written by Nilesh Patra for the Debian distribution and
can be used for any other usage of the program.