BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 19284636)

  • 1. Missing call bias in high-throughput genotyping.
    Fu W; Wang Y; Wang Y; Li R; Lin R; Jin L
    BMC Genomics; 2009 Mar; 10():106. PubMed ID: 19284636
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Validation of pooled genotyping on the Affymetrix 500 k and SNP6.0 genotyping platforms using the polynomial-based probe-specific correction.
    Anantharaman R; Chew FT
    BMC Genet; 2009 Dec; 10():82. PubMed ID: 20003400
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference.
    Saunders IW; Brohede J; Hannan GN
    Genomics; 2007 Sep; 90(3):291-6. PubMed ID: 17587543
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Discovery of novel variants in genotyping arrays improves genotype retention and reduces ascertainment bias.
    Didion JP; Yang H; Sheppard K; Fu CP; McMillan L; de Villena FP; Churchill GA
    BMC Genomics; 2012 Jan; 13():34. PubMed ID: 22260749
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Strategies for processing and quality control of Illumina genotyping arrays.
    Zhao S; Jing W; Samuels DC; Sheng Q; Shyr Y; Guo Y
    Brief Bioinform; 2018 Sep; 19(5):765-775. PubMed ID: 28334151
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests.
    Liu W; Zhao W; Chase GA
    Hum Hered; 2006; 61(1):31-44. PubMed ID: 16557026
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tradeoff between no-call reduction in genotyping error rate and loss of sample size for genetic case/control association studies.
    Kang SJ; Gordon D; Brown AM; Ott J; Finch SJ
    Pac Symp Biocomput; 2004; ():116-27. PubMed ID: 14992497
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The cost effectiveness of duplicate genotyping for testing genetic association.
    Tintle N; Gordon D; Van Bruggen D; Finch S
    Ann Hum Genet; 2009 May; 73(Pt 3):370-8. PubMed ID: 19344449
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Assessing batch effects of genotype calling algorithm BRLMM for the Affymetrix GeneChip Human Mapping 500 K array set using 270 HapMap samples.
    Hong H; Su Z; Ge W; Shi L; Perkins R; Fang H; Xu J; Chen JJ; Han T; Kaput J; Fuscoe JC; Tong W
    BMC Bioinformatics; 2008 Aug; 9 Suppl 9(Suppl 9):S17. PubMed ID: 18793462
    [TBL] [Abstract][Full Text] [Related]  

  • 10. OpenADAM: an open source genome-wide association data management system for Affymetrix SNP arrays.
    Yeung JM; Sham PC; Chan AS; Cherny SS
    BMC Genomics; 2008 Dec; 9():636. PubMed ID: 19117518
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Genotyping-by-sequencing and SNP-arrays are complementary for detecting quantitative trait loci by tagging different haplotypes in association studies.
    Negro SS; Millet EJ; Madur D; Bauland C; Combes V; Welcker C; Tardieu F; Charcosset A; Nicolas SD
    BMC Plant Biol; 2019 Jul; 19(1):318. PubMed ID: 31311506
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Technical reproducibility of genotyping SNP arrays used in genome-wide association studies.
    Hong H; Xu L; Liu J; Jones WD; Su Z; Ning B; Perkins R; Ge W; Miclaus K; Zhang L; Park K; Green B; Han T; Fang H; Lambert CG; Vega SC; Lin SM; Jafari N; Czika W; Wolfinger RD; Goodsaid F; Tong W; Shi L
    PLoS One; 2012; 7(9):e44483. PubMed ID: 22970228
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Estimates of array and pool-construction variance for planning efficient DNA-pooling genome wide association studies.
    Earp MA; Rahmani M; Chew K; Brooks-Wilson A
    BMC Med Genomics; 2011 Nov; 4():81. PubMed ID: 22122996
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Relationship between call rate per individual and genotyping accuracy of bovine single-nucleotide polymorphism array using deoxyribonucleic acid of various qualities.
    Sasaki S; Yoshinari K; Uchiyama K; Takeda M; Kojima T
    Anim Sci J; 2018 Nov; 89(11):1533-1539. PubMed ID: 30230122
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Incorporating duplicate genotype data into linear trend tests of genetic association: methods and cost-effectiveness.
    Borchers B; Brown M; McLellan B; Bekmetjev A; Tintle NL
    Stat Appl Genet Mol Biol; 2009; 8(1):Article24. PubMed ID: 19492982
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Assessing the impact of differential genotyping errors on rare variant tests of association.
    Mayer-Jochimsen M; Fast S; Tintle NL
    PLoS One; 2013; 8(3):e56626. PubMed ID: 23472072
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotyping errors, pedigree errors, and missing data.
    Hinrichs AL; Suarez BK
    Genet Epidemiol; 2005; 29 Suppl 1():S120-4. PubMed ID: 16342180
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.
    Di X; Matsuzaki H; Webster TA; Hubbell E; Liu G; Dong S; Bartell D; Huang J; Chiles R; Yang G; Shen MM; Kulp D; Kennedy GC; Mei R; Jones KW; Cawley S
    Bioinformatics; 2005 May; 21(9):1958-63. PubMed ID: 15657097
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.