Changes between Version 18 and Version 19 of SOPs/variant_calling_GATK
- Timestamp:
- 12/16/15 11:49:33 (9 years ago)
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SOPs/variant_calling_GATK
v18 v19 1 1 === Which mapper and variant caller works best? === 2 2 3 No simple answer , but see3 No simple answer (of course), but see 4 4 * [http://www.ncbi.nlm.nih.gov/pubmed/26639839 Hwang at al., 2015. Systematic comparison of variant calling pipelines using gold standard personal exome variants.] 5 * [http://www.ncbi.nlm.nih.gov/pubmed/25078893 Pirooznia et al., 2014. Validation and assessment of variant calling pipelines for next-generation sequencing.] 6 * [http://www.ncbi.nlm.nih.gov/pubmed/24086590 Liu et al., 2013. Variant callers for next-generation sequencing data: a comparison study.] 7 5 8 6 9 == Using GATK to call variants from short-read sequencing ==