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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...

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Pubblicato in:G3 (Bethesda)
Autori principali: McCormick, Ryan F., Truong, Sandra K., Mullet, John E.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Genetics Society of America 2015
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Accesso online: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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