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stop with an error message if Q values are below or above thresholds
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-9
lines changed

2 files changed

+11
-9
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Lines changed: 5 additions & 4 deletions
Original file line numberDiff line numberDiff line change
@@ -1,6 +1,7 @@
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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.
Lines changed: 6 additions & 5 deletions
Original file line numberDiff line numberDiff line change
@@ -1,7 +1,8 @@
11
`--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
6+
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
8+
and 2.

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