Analysis of archived residual newborn screening blood spots after whole genome amplification

BACKGROUND: Deidentified newborn screening bloodspot samples (NBS) represent a valuable potential resource for genomic research if impediments to whole exome sequencing of NBS deoxyribonucleic acid (DNA), including the small amount of genomic DNA in NBS material, can be overcome. For instance, genom...

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Detalles Bibliográficos
Autores principales: Cantarel, Brandi L., Lei, Yunping, Weaver, Daniel, Zhu, Huiping, Farrell, Andrew, Benstead-Hume, Graeme, Reese, Justin, Finnell, Richard H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535253/
https://www.ncbi.nlm.nih.gov/pubmed/26268606
http://dx.doi.org/10.1186/s12864-015-1747-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535253/
https://www.ncbi.nlm.nih.gov/pubmed/26268606
http://dx.doi.org/10.1186/s12864-015-1747-2

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