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RIG: Recalibration and Interrelation of Genomic Sequence Data with the GATK
Recent advances in variant calling made available in the Genome Analysis Toolkit (GATK) enable the use of validated single-nucleotide polymorphisms and indels to improve variant calling. However, large collections of variants for this purpose often are unavailable to research communities. We introdu...
Gardado en:
| Publicado en: | G3 (Bethesda) |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Genetics Society of America
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4390580/ https://ncbi.nlm.nih.gov/pubmed/25681258 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/g3.115.017012 |
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