These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
203 related articles for article (PubMed ID: 19918757)
21. Imputation of missing genotypes: an empirical evaluation of IMPUTE. Zhao Z; Timofeev N; Hartley SW; Chui DH; Fucharoen S; Perls TT; Steinberg MH; Baldwin CT; Sebastiani P BMC Genet; 2008 Dec; 9():85. PubMed ID: 19077279 [TBL] [Abstract][Full Text] [Related]
22. A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women. Taylor KC; Evans DS; Edwards DRV; Edwards TL; Sofer T; Li G; Liu Y; Franceschini N; Jackson RD; Giri A; Donneyong M; Psaty B; Rotter JI; LaCroix AZ; Jordan JM; Robbins JA; Lewis B; Stefanick ML; Liu Y; Garcia M; Harris T; Cauley JA; North KE Bone Rep; 2016 Dec; 5():233-242. PubMed ID: 28580392 [TBL] [Abstract][Full Text] [Related]
23. Opening the Black Box of Imputation Software to Study the Impact of Reference Panel Composition on Performance. Dekeyser T; Génin E; Herzig AF Genes (Basel); 2023 Feb; 14(2):. PubMed ID: 36833337 [TBL] [Abstract][Full Text] [Related]
24. Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs. Pistis G; Porcu E; Vrieze SI; Sidore C; Steri M; Danjou F; Busonero F; Mulas A; Zoledziewska M; Maschio A; Brennan C; Lai S; Miller MB; Marcelli M; Urru MF; Pitzalis M; Lyons RH; Kang HM; Jones CM; Angius A; Iacono WG; Schlessinger D; McGue M; Cucca F; Abecasis GR; Sanna S Eur J Hum Genet; 2015 Jul; 23(7):975-83. PubMed ID: 25293720 [TBL] [Abstract][Full Text] [Related]
25. A genome-wide association study of serum uric acid in African Americans. Charles BA; Shriner D; Doumatey A; Chen G; Zhou J; Huang H; Herbert A; Gerry NP; Christman MF; Adeyemo A; Rotimi CN BMC Med Genomics; 2011 Feb; 4():17. PubMed ID: 21294900 [TBL] [Abstract][Full Text] [Related]
26. Performance of genotype imputations using data from the 1000 Genomes Project. Sung YJ; Wang L; Rankinen T; Bouchard C; Rao DC Hum Hered; 2012; 73(1):18-25. PubMed ID: 22212296 [TBL] [Abstract][Full Text] [Related]
27. Imputation across genotyping arrays for genome-wide association studies: assessment of bias and a correction strategy. Johnson EO; Hancock DB; Levy JL; Gaddis NC; Saccone NL; Bierut LJ; Page GP Hum Genet; 2013 May; 132(5):509-22. PubMed ID: 23334152 [TBL] [Abstract][Full Text] [Related]
28. Genotype-imputation accuracy across worldwide human populations. Huang L; Li Y; Singleton AB; Hardy JA; Abecasis G; Rosenberg NA; Scheet P Am J Hum Genet; 2009 Feb; 84(2):235-50. PubMed ID: 19215730 [TBL] [Abstract][Full Text] [Related]
30. Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels. Zhou W; Fritsche LG; Das S; Zhang H; Nielsen JB; Holmen OL; Chen J; Lin M; Elvestad MB; Hveem K; Abecasis GR; Kang HM; Willer CJ Genet Epidemiol; 2017 Dec; 41(8):744-755. PubMed ID: 28861891 [TBL] [Abstract][Full Text] [Related]
31. A high-resolution haplotype-resolved Reference panel constructed from the China Kadoorie Biobank Study. Yu C; Lan X; Tao Y; Guo Y; Sun D; Qian P; Zhou Y; Walters RG; Li L; Zhu Y; Zeng J; Millwood IY; Guo R; Pei P; Yang T; Du H; Yang F; Yang L; Ren F; Chen Y; Chen F; Jiang X; Ye Z; Dai L; Wei X; Xu X; Yang H; Wang J; Chen Z; Zhu H; Lv J; Jin X; Li L Nucleic Acids Res; 2023 Nov; 51(21):11770-11782. PubMed ID: 37870428 [TBL] [Abstract][Full Text] [Related]
32. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Li Y; Willer CJ; Ding J; Scheet P; Abecasis GR Genet Epidemiol; 2010 Dec; 34(8):816-34. PubMed ID: 21058334 [TBL] [Abstract][Full Text] [Related]
33. The effect of reference panels and software tools on genotype imputation. Nho K; Shen L; Kim S; Swaminathan S; Risacher SL; Saykin AJ; AMIA Annu Symp Proc; 2011; 2011():1013-8. PubMed ID: 22195161 [TBL] [Abstract][Full Text] [Related]
34. Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle. Rafter P; Gormley IC; Parnell AC; Kearney JF; Berry DP BMC Genomics; 2020 Mar; 21(1):205. PubMed ID: 32131735 [TBL] [Abstract][Full Text] [Related]
35. ATRIUM: testing untyped SNPs in case-control association studies with related individuals. Wang Z; McPeek MS Am J Hum Genet; 2009 Nov; 85(5):667-78. PubMed ID: 19913122 [TBL] [Abstract][Full Text] [Related]
36. Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study. Chen MH; Huang J; Chen WM; Larson MG; Fox CS; Vasan RS; Seshadri S; O'Donnell CJ; Yang Q PLoS One; 2012; 7(12):e51589. PubMed ID: 23284720 [TBL] [Abstract][Full Text] [Related]
37. Increased genetic diversity of ADME genes in African Americans compared with their putative ancestral source populations and implications for pharmacogenomics. Li J; Lao X; Zhang C; Tian L; Lu D; Xu S BMC Genet; 2014 May; 15():52. PubMed ID: 24884825 [TBL] [Abstract][Full Text] [Related]
38. Accuracy of genome-wide imputation in Braford and Hereford beef cattle. Piccoli ML; Braccini J; Cardoso FF; Sargolzaei M; Larmer SG; Schenkel FS BMC Genet; 2014 Dec; 15():157. PubMed ID: 25543517 [TBL] [Abstract][Full Text] [Related]
39. Harmonization of study and reference data by PhaseLift: saving time when imputing study data. Gorski M; Winkler TW; Stark K; Müller-Nurasyid M; Ried JS; Grallert H; Weber BH; Heid IM Genet Epidemiol; 2014 Jul; 38(5):381-8. PubMed ID: 24962562 [TBL] [Abstract][Full Text] [Related]
40. Development of admixture mapping panels for African Americans from commercial high-density SNP arrays. Chen G; Shriner D; Zhou J; Doumatey A; Huang H; Gerry NP; Herbert A; Christman MF; Chen Y; Dunston GM; Faruque MU; Rotimi CN; Adeyemo A BMC Genomics; 2010 Jul; 11():417. PubMed ID: 20602785 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]