135 related articles for article (PubMed ID: 27876820)
1. A method to customize population-specific arrays for genome-wide association testing.
Ehli EA; Abdellaoui A; Fedko IO; Grieser C; Nohzadeh-Malakshah S; Willemsen G; de Geus EJ; Boomsma DI; Davies GE; Hottenga JJ
Eur J Hum Genet; 2017 Feb; 25(2):267-270. PubMed ID: 27876820
[TBL] [Abstract][Full Text] [Related]
2. Effect of genome-wide genotyping and reference panels on rare variants imputation.
Zheng HF; Ladouceur M; Greenwood CM; Richards JB
J Genet Genomics; 2012 Oct; 39(10):545-50. PubMed ID: 23089364
[TBL] [Abstract][Full Text] [Related]
3. Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases.
Xing C; Huang J; Hsu YH; DeStefano AL; Heard-Costa NL; Wolf PA; Seshadri S; Kiel DP; Cupples LA; Dupuis J
Eur J Hum Genet; 2016 Jul; 24(7):1029-34. PubMed ID: 26577045
[TBL] [Abstract][Full Text] [Related]
4. A comparison of genotyping arrays.
Verlouw JAM; Clemens E; de Vries JH; Zolk O; Verkerk AJMH; Am Zehnhoff-Dinnesen A; Medina-Gomez C; Lanvers-Kaminsky C; Rivadeneira F; Langer T; van Meurs JBJ; van den Heuvel-Eibrink MM; Uitterlinden AG; Broer L
Eur J Hum Genet; 2021 Nov; 29(11):1611-1624. PubMed ID: 34140649
[TBL] [Abstract][Full Text] [Related]
5. Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPs.
Sakurai-Yageta M; Kumada K; Gocho C; Makino S; Uruno A; Tadaka S; Motoike IN; Kimura M; Ito S; Otsuki A; Narita A; Kudo H; Aoki Y; Danjoh I; Yasuda J; Kawame H; Minegishi N; Koshiba S; Fuse N; Tamiya G; Yamamoto M; Kinoshita K
J Biochem; 2021 Oct; 170(3):399-410. PubMed ID: 34131746
[TBL] [Abstract][Full Text] [Related]
6. Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individuals.
Kawai Y; Mimori T; Kojima K; Nariai N; Danjoh I; Saito R; Yasuda J; Yamamoto M; Nagasaki M
J Hum Genet; 2015 Oct; 60(10):581-7. PubMed ID: 26108142
[TBL] [Abstract][Full Text] [Related]
7. Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds.
Schaefer RJ; Schubert M; Bailey E; Bannasch DL; Barrey E; Bar-Gal GK; Brem G; Brooks SA; Distl O; Fries R; Finno CJ; Gerber V; Haase B; Jagannathan V; Kalbfleisch T; Leeb T; Lindgren G; Lopes MS; Mach N; da Câmara Machado A; MacLeod JN; McCoy A; Metzger J; Penedo C; Polani S; Rieder S; Tammen I; Tetens J; Thaller G; Verini-Supplizi A; Wade CM; Wallner B; Orlando L; Mickelson JR; McCue ME
BMC Genomics; 2017 Jul; 18(1):565. PubMed ID: 28750625
[TBL] [Abstract][Full Text] [Related]
8. Securing the use of existing sample collections for future human genetic research.
Kanoungi G; Nürnberg P; Nothnagel M
Eur J Hum Genet; 2017 May; 25(5):522-529. PubMed ID: 28145429
[TBL] [Abstract][Full Text] [Related]
9. Development and preliminary evaluation of a 90 K Axiom® SNP array for the allo-octoploid cultivated strawberry Fragaria × ananassa.
Bassil NV; Davis TM; Zhang H; Ficklin S; Mittmann M; Webster T; Mahoney L; Wood D; Alperin ES; Rosyara UR; Koehorst-Vanc Putten H; Monfort A; Sargent DJ; Amaya I; Denoyes B; Bianco L; van Dijk T; Pirani A; Iezzoni A; Main D; Peace C; Yang Y; Whitaker V; Verma S; Bellon L; Brew F; Herrera R; van de Weg E
BMC Genomics; 2015 Mar; 16(1):155. PubMed ID: 25886969
[TBL] [Abstract][Full Text] [Related]
10. Improving accuracy of rare variant imputation with a two-step imputation approach.
Kreiner-Møller E; Medina-Gomez C; Uitterlinden AG; Rivadeneira F; Estrada K
Eur J Hum Genet; 2015 Mar; 23(3):395-400. PubMed ID: 24939589
[TBL] [Abstract][Full Text] [Related]
11. Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'.
Deelen P; Menelaou A; van Leeuwen EM; Kanterakis A; van Dijk F; Medina-Gomez C; Francioli LC; Hottenga JJ; Karssen LC; Estrada K; Kreiner-Møller E; Rivadeneira F; van Setten J; Gutierrez-Achury J; Westra HJ; Franke L; van Enckevort D; Dijkstra M; Byelas H; van Duijn CM; ; de Bakker PI; Wijmenga C; Swertz MA
Eur J Hum Genet; 2014 Nov; 22(11):1321-6. PubMed ID: 24896149
[TBL] [Abstract][Full Text] [Related]
12. Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics.
Wasik K; Berisa T; Pickrell JK; Li JH; Fraser DJ; King K; Cox C
BMC Genomics; 2021 Mar; 22(1):197. PubMed ID: 33743587
[TBL] [Abstract][Full Text] [Related]
13. Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative.
Liu EY; Buyske S; Aragaki AK; Peters U; Boerwinkle E; Carlson C; Carty C; Crawford DC; Haessler J; Hindorff LA; Marchand LL; Manolio TA; Matise T; Wang W; Kooperberg C; North KE; Li Y
Genet Epidemiol; 2012 Feb; 36(2):107-17. PubMed ID: 22851474
[TBL] [Abstract][Full Text] [Related]
14. Low-depth genotyping-by-sequencing (GBS) in a bovine population: strategies to maximize the selection of high quality genotypes and the accuracy of imputation.
Brouard JS; Boyle B; Ibeagha-Awemu EM; Bissonnette N
BMC Genet; 2017 Apr; 18(1):32. PubMed ID: 28381212
[TBL] [Abstract][Full Text] [Related]
15. Development and validation of the Axiom(®) Apple480K SNP genotyping array.
Bianco L; Cestaro A; Linsmith G; Muranty H; Denancé C; Théron A; Poncet C; Micheletti D; Kerschbamer E; Di Pierro EA; Larger S; Pindo M; Van de Weg E; Davassi A; Laurens F; Velasco R; Durel CE; Troggio M
Plant J; 2016 Apr; 86(1):62-74. PubMed ID: 26919684
[TBL] [Abstract][Full Text] [Related]
16. Comparison among three variant callers and assessment of the accuracy of imputation from SNP array data to whole-genome sequence level in chicken.
Ni G; Strom TM; Pausch H; Reimer C; Preisinger R; Simianer H; Erbe M
BMC Genomics; 2015 Oct; 16():824. PubMed ID: 26486989
[TBL] [Abstract][Full Text] [Related]
17. Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples.
Jiang L; Willner D; Danoy P; Xu H; Brown MA
G3 (Bethesda); 2013 Jan; 3(1):23-9. PubMed ID: 23316436
[TBL] [Abstract][Full Text] [Related]
18. Whole-genome characterization in pedigreed non-human primates using genotyping-by-sequencing (GBS) and imputation.
Bimber BN; Raboin MJ; Letaw J; Nevonen KA; Spindel JE; McCouch SR; Cervera-Juanes R; Spindel E; Carbone L; Ferguson B; Vinson A
BMC Genomics; 2016 Aug; 17(1):676. PubMed ID: 27558348
[TBL] [Abstract][Full Text] [Related]
19. Imputation-based genomic coverage assessments of current human genotyping arrays.
Nelson SC; Doheny KF; Pugh EW; Romm JM; Ling H; Laurie CA; Browning SR; Weir BS; Laurie CC
G3 (Bethesda); 2013 Oct; 3(10):1795-807. PubMed ID: 23979933
[TBL] [Abstract][Full Text] [Related]
20. Content and Performance of the MiniMUGA Genotyping Array: A New Tool To Improve Rigor and Reproducibility in Mouse Research.
Sigmon JS; Blanchard MW; Baric RS; Bell TA; Brennan J; Brockmann GA; Burks AW; Calabrese JM; Caron KM; Cheney RE; Ciavatta D; Conlon F; Darr DB; Faber J; Franklin C; Gershon TR; Gralinski L; Gu B; Gaines CH; Hagan RS; Heimsath EG; Heise MT; Hock P; Ideraabdullah F; Jennette JC; Kafri T; Kashfeen A; Kulis M; Kumar V; Linnertz C; Livraghi-Butrico A; Lloyd KCK; Lutz C; Lynch RM; Magnuson T; Matsushima GK; McMullan R; Miller DR; Mohlke KL; Moy SS; Murphy CEY; Najarian M; O'Brien L; Palmer AA; Philpot BD; Randell SH; Reinholdt L; Ren Y; Rockwood S; Rogala AR; Saraswatula A; Sassetti CM; Schisler JC; Schoenrock SA; Shaw GD; Shorter JR; Smith CM; St Pierre CL; Tarantino LM; Threadgill DW; Valdar W; Vilen BJ; Wardwell K; Whitmire JK; Williams L; Zylka MJ; Ferris MT; McMillan L; Manuel de Villena FP
Genetics; 2020 Dec; 216(4):905-930. PubMed ID: 33067325
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
