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 *

82 related articles for article (PubMed ID: 30669964)

  • 1. s-dePooler: determination of polymorphism carriers from overlapping DNA pools.
    Zhernakov AI; Afonin AM; Gavriliuk ND; Moiseeva OM; Zhukov VA
    BMC Bioinformatics; 2019 Jan; 20(1):45. PubMed ID: 30669964
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A statistical method for the detection of variants from next-generation resequencing of DNA pools.
    Bansal V
    Bioinformatics; 2010 Jun; 26(12):i318-24. PubMed ID: 20529923
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Overlapping pools for high-throughput targeted resequencing.
    Prabhu S; Pe'er I
    Genome Res; 2009 Jul; 19(7):1254-61. PubMed ID: 19447964
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Weighted pooling--practical and cost-effective techniques for pooled high-throughput sequencing.
    Golan D; Erlich Y; Rosset S
    Bioinformatics; 2012 Jun; 28(12):i197-206. PubMed ID: 22689761
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rare variant discovery and calling by sequencing pooled samples with overlaps.
    Wang W; Yin X; Soo Pyon Y; Hayes M; Li J
    Bioinformatics; 2013 Jan; 29(1):29-38. PubMed ID: 23104896
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Quantitative group testing-based overlapping pool sequencing to identify rare variant carriers.
    Cao CC; Li C; Sun X
    BMC Bioinformatics; 2014 Jun; 15():195. PubMed ID: 24934981
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identifying rare variants with optimal depth of coverage and cost-effective overlapping pool sequencing.
    Cao CC; Li C; Huang Z; Ma X; Sun X
    Genet Epidemiol; 2013 Dec; 37(8):820-30. PubMed ID: 24166758
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A two-dimensional pooling strategy for rare variant detection on next-generation sequencing platforms.
    Zuzarte PC; Denroche RE; Fehringer G; Katzov-Eckert H; Hung RJ; McPherson JD
    PLoS One; 2014; 9(4):e93455. PubMed ID: 24728235
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variant identification in multi-sample pools by illumina genome analyzer sequencing.
    Margraf RL; Durtschi JD; Dames S; Pattison DC; Stephens JE; Voelkerding KV
    J Biomol Tech; 2011 Jul; 22(2):74-84. PubMed ID: 21738440
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SNPs/pools: a methodology for the identification of relevant SNPs in breast cancer epidemiology.
    Silva SN; Guerreiro D; Gomes M; Azevedo AP; Bezerra De Castro G; Rueff J; Gaspar JF
    Oncol Rep; 2012 Feb; 27(2):511-6. PubMed ID: 22024983
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Practical capability and cost effectiveness of a DNA pool-based genome-wide association study using BovineSNP50 array in a cattle population.
    Uemoto Y; Sasago N; Abe T; Okada H; Maruoka H; Nakajima H; Shoji N; Maruyama S; Kobayashi N; Mannen H; Kobayashi E
    Anim Sci J; 2012 Nov; 83(11):719-26. PubMed ID: 23126324
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PoooL: an efficient method for estimating haplotype frequencies from large DNA pools.
    Zhang H; Yang HC; Yang Y
    Bioinformatics; 2008 Sep; 24(17):1942-8. PubMed ID: 18573795
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A permutation test for oligoset DNA pooling studies.
    Huang HY; Lin JH; Lee WC
    PLoS One; 2015; 10(3):e0119096. PubMed ID: 25763822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An ancestry informative marker panel design for individual ancestry estimation of Hispanic population using whole exome sequencing data.
    Wang LJ; Zhang CW; Su SC; Chen HH; Chiu YC; Lai Z; Bouamar H; Ramirez AG; Cigarroa FG; Sun LZ; Chen Y
    BMC Genomics; 2019 Dec; 20(Suppl 12):1007. PubMed ID: 31888480
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pooled-DNA Sequencing for Elucidating New Genomic Risk Factors, Rare Variants Underlying Alzheimer's Disease.
    Jin SC; Benitez BA; Deming Y; Cruchaga C
    Methods Mol Biol; 2016; 1303():299-314. PubMed ID: 26235075
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An empirical Bayes mixture model for SNP detection in pooled sequencing data.
    Zhou B
    Bioinformatics; 2012 Oct; 28(20):2569-75. PubMed ID: 22914221
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DNA pooling and statistical tests for the detection of single nucleotide polymorphisms.
    Ramsey DM; Futschik A
    Stat Appl Genet Mol Biol; 2012 Sep; 11(5):Article 1. PubMed ID: 23023700
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Large-scale determination of SNP allele frequencies in DNA pools using MALDI-TOF mass spectrometry.
    Werner M; Sych M; Herbon N; Illig T; König IR; Wjst M
    Hum Mutat; 2002 Jul; 20(1):57-64. PubMed ID: 12112658
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC).
    Wolford JK; Blunt D; Ballecer C; Prochazka M
    Hum Genet; 2000 Nov; 107(5):483-7. PubMed ID: 11140946
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evaluation of a new pooling strategy based on leukocyte count for rapid quantification of allele frequencies.
    Rossmann H; Büchler E; Wenzel JJ; Neukirch C; du Prel JB; Lackner KJ
    Clin Chem; 2007 May; 53(5):980-2. PubMed ID: 17412798
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.