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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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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2013
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| Onderwerpen: | |
| Online toegang: | 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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