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Detailed comparison of two popular variant calling packages for exome and targeted exon studies
The Genome Analysis Toolkit (GATK) is commonly used for variant calling of single nucleotide polymorphisms (SNPs) and small insertions and deletions (indels) from short-read sequencing data aligned against a reference genome. There have been a number of variant calling comparisons against GATK, but...
Gorde:
| Egile Nagusiak: | , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
PeerJ Inc.
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4184249/ https://ncbi.nlm.nih.gov/pubmed/25289185 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.600 |
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