BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 18854868)

  • 41. 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]  

  • 42. Joint Estimation of Relatedness Coefficients and Allele Frequencies from Ancient Samples.
    Theunert C; Racimo F; Slatkin M
    Genetics; 2017 Jun; 206(2):1025-1035. PubMed ID: 28396504
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. Effective detection of rare variants in pooled DNA samples using Cross-pool tailcurve analysis.
    Niranjan TS; Adamczyk A; Bravo HC; Taub MA; Wheelan SJ; Irizarry R; Wang T
    Genome Biol; 2011 Sep; 12(9):R93. PubMed ID: 21955804
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Massively parallel exon capture and library-free resequencing across 16 genomes.
    Turner EH; Lee C; Ng SB; Nickerson DA; Shendure J
    Nat Methods; 2009 May; 6(5):315-6. PubMed ID: 19349981
    [No Abstract]   [Full Text] [Related]  

  • 46. Case-control association testing of common variants from sequencing of DNA pools.
    McRae AF; Richter MM; Lind PA
    PLoS One; 2013; 8(6):e65410. PubMed ID: 23762362
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Degradation in forensic trace DNA samples explored by massively parallel sequencing.
    Hanssen EN; Lyle R; Egeland T; Gill P
    Forensic Sci Int Genet; 2017 Mar; 27():160-166. PubMed ID: 28088090
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A new simple method for estimation of allelic frequencies using pooled samples.
    Saadat M; Qasemian-Talgard A; Darvishi FZ; Taghipour N; Saadat I
    Gene; 2019 Jun; 703():13-16. PubMed ID: 30951855
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. Massively parallel sequencing and rare disease.
    Ng SB; Nickerson DA; Bamshad MJ; Shendure J
    Hum Mol Genet; 2010 Oct; 19(R2):R119-24. PubMed ID: 20846941
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Estimation of allele frequencies from high-coverage genome-sequencing projects.
    Lynch M
    Genetics; 2009 May; 182(1):295-301. PubMed ID: 19293142
    [TBL] [Abstract][Full Text] [Related]  

  • 52. On the optimal design of genetic variant discovery studies.
    Ionita-Laza I; Laird NM
    Stat Appl Genet Mol Biol; 2010; 9(1):Article33. PubMed ID: 20812911
    [TBL] [Abstract][Full Text] [Related]  

  • 53. New strategies and emerging technologies for massively parallel sequencing: applications in medical research.
    Mardis ER
    Genome Med; 2009 Apr; 1(4):40. PubMed ID: 19435481
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Advance in DNA pooling application in genetic and molecular epidemiology].
    Hu Y; Hu YH
    Zhonghua Liu Xing Bing Xue Za Zhi; 2010 Jul; 31(7):820-2. PubMed ID: 21162853
    [No Abstract]   [Full Text] [Related]  

  • 55. HUMAN EVOLUTION. Tracking how humans evolve in real time.
    Pennisi E
    Science; 2016 May; 352(6288):876-7. PubMed ID: 27199392
    [No Abstract]   [Full Text] [Related]  

  • 56. Estimation of the covariance structure from SNP allele frequencies.
    van Waaij J; Li Z; Wiuf C
    Stat Appl Genet Mol Biol; 2022 May; 21(1):. PubMed ID: 35634906
    [No Abstract]   [Full Text] [Related]  

  • 57. Genetic variation: Putting causal variants on the map.
    Perdigoto C
    Nat Rev Genet; 2018 Apr; 19(4):188-189. PubMed ID: 29456248
    [No Abstract]   [Full Text] [Related]  

  • 58. Erratum to: More Comprehensive Forensic Genetic Marker Analyses for Accurate Human Remains Identification Using Massively Parallel DNA Sequencing.
    Ambers AD; Churchill JD; King JL; Stoljarova M; Gill-King H; Assidi M; Abu-Elmagd M; Buhmeida A; Al-Qahtani M; Budowle B
    BMC Genomics; 2017 Apr; 18(1):312. PubMed ID: 28427331
    [No Abstract]   [Full Text] [Related]  

  • 59. Supersequencing the supercontrols.
    Nat Genet; 2011 Oct; 43(11):1041. PubMed ID: 22030601
    [No Abstract]   [Full Text] [Related]  

  • 60. Massively Parallel Identification of Regulatory Variants in Asthma.
    Biton A; Torgerson D; Letonqueze O; Zhao W; Zaitlen N; Erle DJ
    Ann Am Thorac Soc; 2016 Mar; 13 Suppl 1(Suppl 1):S104. PubMed ID: 27027944
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.