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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Genetics Society of America
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390580/ https://www.ncbi.nlm.nih.gov/pubmed/25681258 http://dx.doi.org/10.1534/g3.115.017012 |