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author | thondeboer |
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date | Wed, 16 May 2018 02:05:26 -0400 |
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# models Used by genReads.py for simulating various characteristics of NGS datasets. ## mutation models * Used via '-m' parameter **MutModel_NA12878.p** - Mimic mutations via statistics derived from NA12878 germline variant calls. (Note that due to filesize restrictions, this one will need to be unzipped first) **MutModel_BRCA_US_ICGC.p** - Aggregate breast cancer mutation statistics from deidentified ICGC data. **MutModel_CLLE-ES_ICGC.p** - Aggregate leukemia mutation statistics from deidentified ICGC data. **MutModel_SKCM-US_ICGC.p** - Aggregate melanoma mutation statistics from deidentified ICGC data. ## sequencing error models * Used via '-e' parameter **errorModel_toy.p** - Sequencing error statistics derived from in-house NGS data. ## paired-end fragment length distribution model * Used via '--pe-model' parameter **fraglenModel_toy.p** - Fragment length statistics derived from in-house NGS data. ## GC% coverage bias model * Used via '--gc-model' parameter **gcBias_toy.p** - GC% coverage bias statistics derived from in-house NGS data.