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@@ -154,6 +154,7 @@ sequenceFolder| string | **REQUIRED** | The folder containing the sequences to a
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minimumCombinedReadLength| integer | **REQUIRED** | The length of the amplified sequence target plus overlap **not including primers**. User is required to set this.
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forwardPrimerLength | integer | **REQUIRED** | The length of the forward primer. User is required to set this.
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reversePrimerLength | integer | **REQUIRED** | The length of the reverse primer. User is required to set this.
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minimumOverlap | integer | 20 | The minimum length of overlap desired for read merging
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fileNamingStandard | string | illumina | Naming convention for files. Currently supporting Illumina and Zymo Services (zymo). Others can be added as requested.--outputFileName | -n | string | trimParameters.json | The desired name of the JSON list of trim parameters and their scores
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subsample | integer | *See description* | What fraction of reads to analyze (1/x) from the FASTQ files. Default value will call a function that sets this based upon the size of the fastq files for a sliding scale.
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percentile | integer | 83 | The percentile to target for read filtering. The default value of 83 will remove reads that are about 1 standard deviation worse than the average read for that direction in that position. You can generally expect a few percentage points below your percentile value of reads to pass the filtering.
Copy file name to clipboardexpand all lines: figaro.py
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importlogging
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from . importfigaroSupport
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try: #This block is here to handle importing issues that happen when running this as a python package vs. running in a Docker or directly from the commandline.
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