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 *

165 related articles for article (PubMed ID: 24088264)

  • 21. Analysis and optimal design for association studies using next-generation sequencing with case-control pools.
    Liang WE; Thomas DC; Conti DV
    Genet Epidemiol; 2012 Dec; 36(8):870-81. PubMed ID: 22972696
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of disease causing loci using an array-based genotyping approach on pooled DNA.
    Craig DW; Huentelman MJ; Hu-Lince D; Zismann VL; Kruer MC; Lee AM; Puffenberger EG; Pearson JM; Stephan DA
    BMC Genomics; 2005 Sep; 6():138. PubMed ID: 16197552
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Microarray-based estimation of SNP allele-frequency in pooled DNA using the Langmuir kinetic model.
    Yin BC; Li H; Ye BC
    BMC Genomics; 2008 Dec; 9():605. PubMed ID: 19087310
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Biases and errors on allele frequency estimation and disease association tests of next-generation sequencing of pooled samples.
    Chen X; Listman JB; Slack FJ; Gelernter J; Zhao H
    Genet Epidemiol; 2012 Sep; 36(6):549-60. PubMed ID: 22674656
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Design of association studies with pooled or un-pooled next-generation sequencing data.
    Kim SY; Li Y; Guo Y; Li R; Holmkvist J; Hansen T; Pedersen O; Wang J; Nielsen R
    Genet Epidemiol; 2010 Jul; 34(5):479-91. PubMed ID: 20552648
    [TBL] [Abstract][Full Text] [Related]  

  • 26. QSNPlite, a software system for quantitative analysis of SNPs based on capillary array SSCP analysis.
    Tahira T; Okazaki Y; Miura K; Yoshinaga A; Masumoto K; Higasa K; Kukita Y; Hayashi K
    Electrophoresis; 2006 Oct; 27(19):3869-78. PubMed ID: 16960832
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pooled DNA genotyping on Affymetrix SNP genotyping arrays.
    Kirov G; Nikolov I; Georgieva L; Moskvina V; Owen MJ; O'Donovan MC
    BMC Genomics; 2006 Feb; 7():27. PubMed ID: 16480507
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genomic relationships computed from either next-generation sequence or array SNP data.
    PĂ©rez-Enciso M
    J Anim Breed Genet; 2014 Apr; 131(2):85-96. PubMed ID: 24397314
    [TBL] [Abstract][Full Text] [Related]  

  • 29. PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays.
    Brohede J; Dunne R; McKay JD; Hannan GN
    Nucleic Acids Res; 2005 Sep; 33(17):e142. PubMed ID: 16199750
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Estimation of relative allele frequencies of single-nucleotide polymorphisms in different populations by microarray hybridization of pooled DNA.
    Bang-Ce Y; Peng Z; Bincheng Y; Songyang L
    Anal Biochem; 2004 Oct; 333(1):72-8. PubMed ID: 15351282
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Assessing allele frequencies of single nucleotide polymorphisms in DNA pools by pyrosequencing technology.
    Wasson J; Skolnick G; Love-Gregory L; Permutt MA
    Biotechniques; 2002 May; 32(5):1144-6, 1148, 1150 passim. PubMed ID: 12019788
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Single nucleotide polymorphism (SNP) allele frequency estimation in DNA pools using Pyrosequencing.
    Lavebratt C; Sengul S
    Nat Protoc; 2006; 1(6):2573-82. PubMed ID: 17406511
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Usefulness of direct sequencing of pooled DNA for SNP identification and allele-frequency determination compatible with a common disease/common variant hypothesis.
    Kim MK; Nam TS; Choi KH; Jang SY; Kim YO; Lee MC
    Genet Mol Res; 2010 Apr; 9(2):772-9. PubMed ID: 20449810
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Large scale single nucleotide polymorphism discovery in unsequenced genomes using second generation high throughput sequencing technology: applied to turkey.
    Kerstens HH; Crooijmans RP; Veenendaal A; Dibbits BW; Chin-A-Woeng TF; den Dunnen JT; Groenen MA
    BMC Genomics; 2009 Oct; 10():479. PubMed ID: 19835600
    [TBL] [Abstract][Full Text] [Related]  

  • 35. PDA: Pooled DNA analyzer.
    Yang HC; Pan CC; Lin CY; Fann CS
    BMC Bioinformatics; 2006 Apr; 7():233. PubMed ID: 16643673
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Estimation of allele frequency in pooled DNA by using PCR-RFLP combined with microchip electrophoresis.
    Wang WP; Zhang RH; Wu P; Wang S; Li R
    J Chromatogr B Analyt Technol Biomed Life Sci; 2009 May; 877(14-15):1603-6. PubMed ID: 19398388
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Validation of Pooled Whole-Genome Re-Sequencing in Arabidopsis lyrata.
    Fracassetti M; Griffin PC; Willi Y
    PLoS One; 2015; 10(10):e0140462. PubMed ID: 26461136
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.
    Chiang CW; Gajdos ZK; Korn JM; Butler JL; Hackett R; Guiducci C; Nguyen TT; Wilks R; Forrester T; Henderson KD; Le Marchand L; Henderson BE; Haiman CA; Cooper RS; Lyon HN; Zhu X; McKenzie CA; Palmert MR; Hirschhorn JN
    Hum Genet; 2011 Nov; 130(5):607-21. PubMed ID: 21424828
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Estimating the effect of SNP genotype on quantitative traits from pooled DNA samples.
    Henshall JM; Hawken RJ; Dominik S; Barendse W
    Genet Sel Evol; 2012 Apr; 44(1):12. PubMed ID: 22507187
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.