A SNP profiling panel for sample tracking in whole-exome sequencing studies

Whole-exome sequencing provides a cost-effective means to sequence protein coding regions within the genome, which are significantly enriched for etiological variants. We describe a panel of single nucleotide polymorphisms (SNPs) to facilitate the validation of data provenance in whole-exome sequenc...

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Hlavní autoři: Pengelly, Reuben J, Gibson, Jane, Andreoletti, Gaia, Collins, Andrew, Mattocks, Christopher J, Ennis, Sarah
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2013
Témata:
Method
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3978886/
https://ncbi.nlm.nih.gov/pubmed/24070238
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm492
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