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 *

148 related articles for article (PubMed ID: 19447964)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. On optimal pooling designs to identify rare variants through massive resequencing.
    Lee JS; Choi M; Yan X; Lifton RP; Zhao H
    Genet Epidemiol; 2011 Apr; 35(3):139-47. PubMed ID: 21254222
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Use of overlapping DNA pools to discern genetic differences despite pooling error.
    Keele JW; McDaneld TG; Kuehn LA
    J Anim Sci; 2023 Jan; 101():. PubMed ID: 37227930
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of rare genomic variants from pooled sequencing using SPLINTER.
    Vallania F; Ramos E; Cresci S; Mitra RD; Druley TE
    J Vis Exp; 2012 Jun; (64):. PubMed ID: 22760212
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Identification of rare alleles and their carriers using compressed se(que)nsing.
    Shental N; Amir A; Zuk O
    Nucleic Acids Res; 2010 Oct; 38(19):e179. PubMed ID: 20699269
    [TBL] [Abstract][Full Text] [Related]  

  • 14. High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools.
    Mohlke KL; Erdos MR; Scott LJ; Fingerlin TE; Jackson AU; Silander K; Hollstein P; Boehnke M; Collins FS
    Proc Natl Acad Sci U S A; 2002 Dec; 99(26):16928-33. PubMed ID: 12482934
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An evaluation of different target enrichment methods in pooled sequencing designs for complex disease association studies.
    Day-Williams AG; McLay K; Drury E; Edkins S; Coffey AJ; Palotie A; Zeggini E
    PLoS One; 2011; 6(11):e26279. PubMed ID: 22069447
    [TBL] [Abstract][Full Text] [Related]  

  • 16. HAPLOPOOL: improving haplotype frequency estimation through DNA pools and phylogenetic modeling.
    Kirkpatrick B; Armendariz CS; Karp RM; Halperin E
    Bioinformatics; 2007 Nov; 23(22):3048-55. PubMed ID: 17895275
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies.
    Daniels J; Holmans P; Williams N; Turic D; McGuffin P; Plomin R; Owen MJ
    Am J Hum Genet; 1998 May; 62(5):1189-97. PubMed ID: 9545387
    [TBL] [Abstract][Full Text] [Related]  

  • 19. How to optimize the precision of allele and haplotype frequency estimates using pooled-sequencing data.
    Rode NO; Holtz Y; Loridon K; Santoni S; Ronfort J; Gay L
    Mol Ecol Resour; 2018 Mar; 18(2):194-203. PubMed ID: 28977733
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A comparison of DNA pools constructed following whole genome amplification for two-stage SNP genotyping designs.
    Zhao ZZ; Nyholt DR; James MR; Mayne R; Treloar SA; Montgomery GW
    Twin Res Hum Genet; 2005 Aug; 8(4):353-61. PubMed ID: 16176720
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.