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SMaSH: Sample matching using SNPs in humans
BACKGROUND: Inadvertent sample swaps are a real threat to data quality in any medium to large scale omics studies. While matches between samples from the same individual can in principle be identified from a few well characterized single nucleotide polymorphisms (SNPs), omics data types often only p...
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| Publicado no: | BMC Genomics |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6936078/ https://ncbi.nlm.nih.gov/pubmed/31888490 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-019-6332-7 |
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