qualityScores1
Toolkit for processing next-gen sequencing data
Overview
qualityScore Version 2.0.4
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Retrieve Phred score for read bases
Usage:
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./qualityScores [options]
-i<input_file>-o<output_file>
Required arguments:
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-i <string> -
Name of input file including read data. The default format is Fastq.
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-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.
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--BAMinput -
Input file is in BAM format.
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--SAMinput -
Input file is in SAM format.
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--first-end -
Use only first reads in paired-end data. Only applicable for paired-end BAM/SAM input.
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--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
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file. 10,000 by default.
--phred-offset <33|64> refer to subread aligner.
Releases
5 releases since Debian 9 (Stretch); the text changed 4 times.
--BAMinput since Debian 12 (Bookworm);
--SAMinput since Debian 12 (Bookworm);
--first-end since Debian 12 (Bookworm);
--second-end since Debian 12 (Bookworm);
-i since Debian 12 (Bookworm);
-o since Debian 12 (Bookworm).