1K08CA140720-01A1/CA/NCI NIH HHS/United States[Grants and Funding] - Search Results

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Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing.

Ramos E, Levinson BT, Chasnoff S, Hughes A, Young AL, Thornton K, Li A, Vallania FL, Province M, Druley TE. Ramos E, et al. BMC Genomics. 2012 Dec 6;13:683. doi: 10.1186/1471-2164-13-683. BMC Genomics. 2012. PMID: 23216810 Free PMC article.

Detection of rare genomic variants from pooled sequencing using SPLINTER.

Vallania F, Ramos E, Cresci S, Mitra RD, Druley TE. Vallania F, et al. J Vis Exp. 2012 Jun 23;(64):3943. doi: 10.3791/3943. J Vis Exp. 2012. PMID: 22760212 Free PMC article.

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