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7. SNP cherry picker: maximizing the chance of finding an association with a disease SNP. Harris M; Martin JM; Peden JF; Rawlings CJ Bioinformatics; 2003 Nov; 19(16):2141-3. PubMed ID: 14594720 [TBL] [Abstract][Full Text] [Related]
8. The exome factor. Stower H Genome Biol; 2011 Sep; 12(9):407. PubMed ID: 21920053 [TBL] [Abstract][Full Text] [Related]
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17. Genome-wide significance testing of variation from single case exomes. Wilfert AB; Chao KR; Kaushal M; Jain S; Zöllner S; Adams DR; Conrad DF Nat Genet; 2016 Dec; 48(12):1455-1461. PubMed ID: 27776118 [TBL] [Abstract][Full Text] [Related]
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19. Personal genomics: his daughter's DNA. Maher B Nature; 2007 Oct; 449(7164):773-6. PubMed ID: 17968422 [No Abstract] [Full Text] [Related]
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