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 *

111 related articles for article (PubMed ID: 23509783)

  • 1. Simpute: an efficient solution for dense genotypic data.
    Lin YJ; Chang CT; Tang CY; Hsieh WP
    Biomed Res Int; 2013; 2013():813912. PubMed ID: 23509783
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Analyses and comparison of accuracy of different genotype imputation methods.
    Pei YF; Li J; Zhang L; Papasian CJ; Deng HW
    PLoS One; 2008; 3(10):e3551. PubMed ID: 18958166
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.
    Xiao Y; Segal MR; Yang YH; Yeh RF
    Bioinformatics; 2007 Jun; 23(12):1459-67. PubMed ID: 17459966
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Quick, "imputation-free" meta-analysis with proxy-SNPs.
    Meesters C; Leber M; Herold C; Angisch M; Mattheisen M; Drichel D; Lacour A; Becker T
    BMC Bioinformatics; 2012 Sep; 13():231. PubMed ID: 22971100
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Evaluating Imputation Algorithms for Low-Depth Genotyping-By-Sequencing (GBS) Data.
    Chan AW; Hamblin MT; Jannink JL
    PLoS One; 2016; 11(8):e0160733. PubMed ID: 27537694
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Selecting additional tag SNPs for tolerating missing data in genotyping.
    Huang YT; Zhang K; Chen T; Chao KM
    BMC Bioinformatics; 2005 Nov; 6():263. PubMed ID: 16259642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comprehensive Assessment of Genotype Imputation Performance.
    Shi S; Yuan N; Yang M; Du Z; Wang J; Sheng X; Wu J; Xiao J
    Hum Hered; 2018; 83(3):107-116. PubMed ID: 30669139
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Genotype imputation via matrix completion.
    Chi EC; Zhou H; Chen GK; Del Vecchyo DO; Lange K
    Genome Res; 2013 Mar; 23(3):509-18. PubMed ID: 23233546
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A comprehensive evaluation of SNP genotype imputation.
    Nothnagel M; Ellinghaus D; Schreiber S; Krawczak M; Franke A
    Hum Genet; 2009 Mar; 125(2):163-71. PubMed ID: 19089453
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Highly Accurate and Efficient Data-Driven Methods for Genotype Imputation.
    Choudhury O; Chakrabarty A; Emrich SJ
    IEEE/ACM Trans Comput Biol Bioinform; 2019; 16(4):1107-1116. PubMed ID: 28574365
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. fcGENE: a versatile tool for processing and transforming SNP datasets.
    Roshyara NR; Scholz M
    PLoS One; 2014; 9(7):e97589. PubMed ID: 25050709
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data.
    Yang WY; Hormozdiari F; Wang Z; He D; Pasaniuc B; Eskin E
    Bioinformatics; 2013 Sep; 29(18):2245-52. PubMed ID: 23825370
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genotype calling algorithm for affymetrix SNP arrays.
    Rabbee N; Speed TP
    Bioinformatics; 2006 Jan; 22(1):7-12. PubMed ID: 16267090
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. GeneImp: Fast Imputation to Large Reference Panels Using Genotype Likelihoods from Ultralow Coverage Sequencing.
    Spiliopoulou A; Colombo M; Orchard P; Agakov F; McKeigue P
    Genetics; 2017 May; 206(1):91-104. PubMed ID: 28348060
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.