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 *

132 related articles for article (PubMed ID: 19284636)

  • 41. Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels.
    Lupton MK; Medland SE; Gordon SD; Goncalves T; MacGregor S; Mackey DA; Young TL; Duffy DL; Visscher PM; Wray NR; Nyholt DR; Bain L; Ferreira MA; Henders AK; Wallace L; Montgomery GW; Wright MJ; Martin NG
    J Alzheimers Dis; 2018; 64(1):49-54. PubMed ID: 29865051
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Assessment and management of single nucleotide polymorphism genotype errors in genetic association analysis.
    Gordon D; Ott J
    Pac Symp Biocomput; 2001; ():18-29. PubMed ID: 11262939
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping.
    Pluzhnikov A; Below JE; Konkashbaev A; Tikhomirov A; Kistner-Griffin E; Roe CA; Nicolae DL; Cox NJ
    Am J Hum Genet; 2010 Jul; 87(1):123-8. PubMed ID: 20598280
    [TBL] [Abstract][Full Text] [Related]  

  • 44. SNiPer: improved SNP genotype calling for Affymetrix 10K GeneChip microarray data.
    Huentelman MJ; Craig DW; Shieh AD; Corneveaux JJ; Hu-Lince D; Pearson JV; Stephan DA
    BMC Genomics; 2005 Oct; 6():149. PubMed ID: 16262895
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Effect of genotyping error in model-free linkage analysis using microsatellite or single-nucleotide polymorphism marker maps.
    Thompson CL; Baechle D; Lu Q; Mathew G; Song Y; Iyengar SK; Gray-McGuire C; Goddard KA
    BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S153. PubMed ID: 16451614
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Power analysis for genome-wide association studies.
    Klein RJ
    BMC Genet; 2007 Aug; 8():58. PubMed ID: 17725844
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Whole-genome amplification enables accurate genotyping for microarray-based high-density single nucleotide polymorphism array.
    Jasmine F; Ahsan H; Andrulis IL; John EM; Chang-Claude J; Kibriya MG
    Cancer Epidemiol Biomarkers Prev; 2008 Dec; 17(12):3499-508. PubMed ID: 19064567
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Fast score test with global null estimation regardless of missing genotypes.
    Sato S; Ueki M;
    PLoS One; 2018; 13(7):e0199692. PubMed ID: 29975732
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Development and characterization of a high density SNP genotyping assay for cattle.
    Matukumalli LK; Lawley CT; Schnabel RD; Taylor JF; Allan MF; Heaton MP; O'Connell J; Moore SS; Smith TP; Sonstegard TS; Van Tassell CP
    PLoS One; 2009; 4(4):e5350. PubMed ID: 19390634
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Deviations from hardy-weinberg equilibrium in parental and unaffected sibling genotype data.
    Li B; Leal SM
    Hum Hered; 2009; 67(2):104-15. PubMed ID: 19077427
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Disentangling pooled triad genotypes for association studies.
    Shi M; Umbach DM; Weinberg CR
    Ann Hum Genet; 2014 Sep; 78(5):345-56. PubMed ID: 24962618
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Bayesian trio models for association in the presence of genotyping errors.
    Bernardinelli L; Berzuini C; Seaman S; Holmans P
    Genet Epidemiol; 2004 Jan; 26(1):70-80. PubMed ID: 14691958
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Susceptibility of biallelic haplotype and genotype frequencies to genotyping error.
    Moskvina V; Schmidt KM
    Biometrics; 2006 Dec; 62(4):1116-23. PubMed ID: 17156286
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Genome-wide association database developed in the Japanese Integrated Database Project.
    Koike A; Nishida N; Inoue I; Tsuji S; Tokunaga K
    J Hum Genet; 2009 Sep; 54(9):543-6. PubMed ID: 19629137
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Parametric model-based statistics for possible genotyping errors and sample stratification in sibling-pair SNP data.
    Korostishevsky M; Malkin I; Spector T; Livshits G
    Genet Epidemiol; 2010 Jan; 34(1):26-33. PubMed ID: 19455577
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Evaluating the influence of quality control decisions and software algorithms on SNP calling for the affymetrix 6.0 SNP array platform.
    de Andrade M; Atkinson EJ; Bamlet WR; Matsumoto ME; Maharjan S; Slager SL; Vachon CM; Cunningham JM; Kardia SL
    Hum Hered; 2011; 71(4):221-33. PubMed ID: 21734406
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The COPILOT Raw Illumina Genotyping QC Protocol.
    Patel H; Lee SH; Breen G; Menzel S; Ojewunmi O; Dobson RJB
    Curr Protoc; 2022 Apr; 2(4):e373. PubMed ID: 35452565
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Using DNA pools for genotyping trios.
    Beckman KB; Abel KJ; Braun A; Halperin E
    Nucleic Acids Res; 2006; 34(19):e129. PubMed ID: 17020923
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A method to address differential bias in genotyping in large-scale association studies.
    Plagnol V; Cooper JD; Todd JA; Clayton DG
    PLoS Genet; 2007 May; 3(5):e74. PubMed ID: 17511519
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.