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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 38221906)

  • 1. Genotype imputation accuracy and the quality metrics of the minor ancestry in multi-ancestry reference panels.
    Shi M; Tanikawa C; Munter HM; Akiyama M; Koyama S; Tomizuka K; Matsuda K; Lathrop GM; Terao C; Koido M; Kamatani Y
    Brief Bioinform; 2023 Nov; 25(1):. PubMed ID: 38221906
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Investigating the accuracy of imputing autosomal variants in Nellore cattle using the ARS-UCD1.2 assembly of the bovine genome.
    Hermisdorff IDC; Costa RB; de Albuquerque LG; Pausch H; Kadri NK
    BMC Genomics; 2020 Nov; 21(1):772. PubMed ID: 33167856
    [TBL] [Abstract][Full Text] [Related]  

  • 3. MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric.
    Sun Q; Yang Y; Rosen JD; Chen J; Li X; Guan W; Jiang MZ; Wen J; Pace RG; Blackman SM; Bamshad MJ; Gibson RL; Cutting GR; O'Neal WK; Knowles MR; Kooperberg C; Reiner AP; Raffield LM; Carson AP; Rich SS; Rotter JI; Loos RJF; Kenny E; Jaeger BC; Min YI; Fuchsberger C; Li Y
    Am J Hum Genet; 2024 May; 111(5):990-995. PubMed ID: 38636510
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Imputation accuracy across global human populations.
    Cahoon JL; Rui X; Tang E; Simons C; Langie J; Chen M; Lo YC; Chiang CWK
    Am J Hum Genet; 2024 May; 111(5):979-989. PubMed ID: 38604166
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Genotype imputation performance of three reference panels using African ancestry individuals.
    Vergara C; Parker MM; Franco L; Cho MH; Valencia-Duarte AV; Beaty TH; Duggal P
    Hum Genet; 2018 Apr; 137(4):281-292. PubMed ID: 29637265
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
    Kowalski MH; Qian H; Hou Z; Rosen JD; Tapia AL; Shan Y; Jain D; Argos M; Arnett DK; Avery C; Barnes KC; Becker LC; Bien SA; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Buyske S; Cai J; Cho MH; Choi SH; Choquet H; Cupples LA; Cushman M; Daya M; de Vries PS; Ellinor PT; Faraday N; Fornage M; Gabriel S; Ganesh SK; Graff M; Gupta N; He J; Heckbert SR; Hidalgo B; Hodonsky CJ; Irvin MR; Johnson AD; Jorgenson E; Kaplan R; Kardia SLR; Kelly TN; Kooperberg C; Lasky-Su JA; Loos RJF; Lubitz SA; Mathias RA; McHugh CP; Montgomery C; Moon JY; Morrison AC; Palmer ND; Pankratz N; Papanicolaou GJ; Peralta JM; Peyser PA; Rich SS; Rotter JI; Silverman EK; Smith JA; Smith NL; Taylor KD; Thornton TA; Tiwari HK; Tracy RP; Wang T; Weiss ST; Weng LC; Wiggins KL; Wilson JG; Yanek LR; Zöllner S; North KE; Auer PL; ; ; Raffield LM; Reiner AP; Li Y
    PLoS Genet; 2019 Dec; 15(12):e1008500. PubMed ID: 31869403
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Evaluation of the accuracy of imputed sequence variant genotypes and their utility for causal variant detection in cattle.
    Pausch H; MacLeod IM; Fries R; Emmerling R; Bowman PJ; Daetwyler HD; Goddard ME
    Genet Sel Evol; 2017 Feb; 49(1):24. PubMed ID: 28222685
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. The feasibility of using low-density marker panels for genotype imputation and genomic prediction of crossbred dairy cattle of East Africa.
    Aliloo H; Mrode R; Okeyo AM; Ni G; Goddard ME; Gibson JP
    J Dairy Sci; 2018 Oct; 101(10):9108-9127. PubMed ID: 30077450
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MagicalRsq: Machine-learning-based genotype imputation quality calibration.
    Sun Q; Yang Y; Rosen JD; Jiang MZ; Chen J; Liu W; Wen J; Raffield LM; Pace RG; Zhou YH; Wright FA; Blackman SM; Bamshad MJ; Gibson RL; Cutting GR; Knowles MR; Schrider DR; Fuchsberger C; Li Y
    Am J Hum Genet; 2022 Nov; 109(11):1986-1997. PubMed ID: 36198314
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Imputation Accuracy Across Global Human Populations.
    Cahoon JL; Rui X; Tang E; Simons C; Langie J; Chen M; Lo YC; Chiang CWK
    bioRxiv; 2023 Oct; ():. PubMed ID: 37292811
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing.
    Hanks SC; Forer L; Schönherr S; LeFaive J; Martins T; Welch R; Gagliano Taliun SA; Braff D; Johnsen JM; Kenny EE; Konkle BA; Laakso M; Loos RFJ; McCarroll S; Pato C; Pato MT; Smith AV; ; Boehnke M; Scott LJ; Fuchsberger C
    Am J Hum Genet; 2022 Sep; 109(9):1653-1666. PubMed ID: 35981533
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population.
    Mauleekoonphairoj J; Tongsima S; Khongphatthanayothin A; Jurgens SJ; Zimmerman DS; Sutjaporn B; Wandee P; Bezzina CR; Nademanee K; Poovorawan Y
    Sci Rep; 2023 Jul; 13(1):12360. PubMed ID: 37524845
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comprehensive evaluation of imputation performance in African Americans.
    Chanda P; Yuhki N; Li M; Bader JS; Hartz A; Boerwinkle E; Kao WH; Arking DE
    J Hum Genet; 2012 Jul; 57(7):411-21. PubMed ID: 22648186
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comparison of multiple imputation and other methods for the analysis of imputed genotypes.
    Auer PL; Wang G; Li G; DeWan AT; Leal SM
    BMC Genomics; 2023 Jun; 24(1):303. PubMed ID: 37277705
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analyzing the Korean reference genome with meta-imputation increased the imputation accuracy and spectrum of rare variants in the Korean population.
    Hwang MY; Choi NH; Won HH; Kim BJ; Kim YJ
    Front Genet; 2022; 13():1008646. PubMed ID: 36506321
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Performance and accuracy evaluation of reference panels for genotype imputation in sub-Saharan African populations.
    Sengupta D; Botha G; Meintjes A; Mbiyavanga M; ; ; Hazelhurst S; Mulder N; Ramsay M; Choudhury A
    Cell Genom; 2023 Jun; 3(6):100332. PubMed ID: 37388906
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.