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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Detalles Bibliográficos
Autores principales: Westphal, Maximillian, Frankhouser, David, Sonzone, Carmine, Shields, Peter G., Yan, Pearlly, Bundschuh, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936078/
https://www.ncbi.nlm.nih.gov/pubmed/31888490
http://dx.doi.org/10.1186/s12864-019-6332-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936078/
https://www.ncbi.nlm.nih.gov/pubmed/31888490
http://dx.doi.org/10.1186/s12864-019-6332-7

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