Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data

We applied our method of pairwise shared genomic segment (pSGS) analysis to high-risk pedigrees identified from the Genetic Analysis Workshop 17 (GAW17) mini-exome sequencing data set. The original shared genomic segment method focused on identifying regions shared by all case subjects in a pedigree...

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Detalles Bibliográficos
Autores principales: Cai, Zheng, Knight, Stacey, Thomas, Alun, Camp, Nicola J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287931/
https://www.ncbi.nlm.nih.gov/pubmed/22373081
http://dx.doi.org/10.1186/1753-6561-5-S9-S9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287931/
https://www.ncbi.nlm.nih.gov/pubmed/22373081
http://dx.doi.org/10.1186/1753-6561-5-S9-S9

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