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` --fastq_qmax ` * positive integer*
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: Specify the maximal quality score accepted when reading fastq
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- sequences. Reads with higher quality scores are discarded. Accepted
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- values range from 0 to 93 if the offset is 33 (see ` --fastq_ascii ` ),
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- or range from 0 to 62 if the offset is 64. The default is 41, which
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- is usual for recent Sanger/Illumina 1.8+ files.
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+ sequences. Stop with an error message if a quality scores higher
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+ than the specified value is read. Accepted values range from 0 to 93
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+ if the offset is 33 (see ` --fastq_ascii ` ), or range from 0 to 62 if
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+ the offset is 64. The default is 41, which is usual for recent
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+ Sanger/Illumina 1.8+ files.
Original file line number Diff line number Diff line change 1
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` --fastq_qmin ` * positive integer*
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: Specify the minimal quality score accepted when reading fastq
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- sequences. Reads with lower quality scores are discarded. Accepted
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- values range from 0 to 93 if the offset is 33 (see ` --fastq_ascii ` ),
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- or range from 0 to 62 if the offset is 64. The default is 0, which
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- is usual for recent Sanger/Illumina 1.8+ files. Older formats may
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- use scores between -5 and 2.
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+ sequences. Stop with an error message if a quality scores lower than
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+ the specified value is read. Accepted values range from 0 to 93 if
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+ the offset is 33 (see ` --fastq_ascii ` ), or range from 0 to 62 if the
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+ offset is 64. The default is 0, which is usual for recent
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+ Sanger/Illumina 1.8+ files. Older formats may use scores between -5
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+ and 2.
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