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 *

152 related articles for article (PubMed ID: 19435481)

  • 21. Advances in clinical next-generation sequencing: target enrichment and sequencing technologies.
    Ballester LY; Luthra R; Kanagal-Shamanna R; Singh RR
    Expert Rev Mol Diagn; 2016; 16(3):357-72. PubMed ID: 26680590
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Preparation of genome-wide DNA fragment libraries using bisulfite in polyacrylamide gel electrophoresis slices with formamide denaturation and quality control for massively parallel sequencing by oligonucleotide ligation and detection.
    Ranade SS; Chung CB; Zon G; Boyd VL
    Anal Biochem; 2009 Jul; 390(2):126-35. PubMed ID: 19379703
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Target capture enrichment of nuclear SNP markers for massively parallel sequencing of degraded and mixed samples.
    Bose N; Carlberg K; Sensabaugh G; Erlich H; Calloway C
    Forensic Sci Int Genet; 2018 May; 34():186-196. PubMed ID: 29524767
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Analysis of the genetic diversity of influenza A viruses using next-generation DNA sequencing.
    Van den Hoecke S; Verhelst J; Vuylsteke M; Saelens X
    BMC Genomics; 2015 Feb; 16(1):79. PubMed ID: 25758772
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Next-Generation Sequencing and Emerging Technologies.
    Kumar KR; Cowley MJ; Davis RL
    Semin Thromb Hemost; 2019 Oct; 45(7):661-673. PubMed ID: 31096307
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Targeted single molecule mutation detection with massively parallel sequencing.
    Gregory MT; Bertout JA; Ericson NG; Taylor SD; Mukherjee R; Robins HS; Drescher CW; Bielas JH
    Nucleic Acids Res; 2016 Feb; 44(3):e22. PubMed ID: 26384417
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Evaluating somatic tumor mutation detection without matched normal samples.
    Teer JK; Zhang Y; Chen L; Welsh EA; Cress WD; Eschrich SA; Berglund AE
    Hum Genomics; 2017 Sep; 11(1):22. PubMed ID: 28870239
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Applications of Probe Capture Enrichment Next Generation Sequencing for Whole Mitochondrial Genome and 426 Nuclear SNPs for Forensically Challenging Samples.
    Shih SY; Bose N; Gonçalves ABR; Erlich HA; Calloway CD
    Genes (Basel); 2018 Jan; 9(1):. PubMed ID: 29361782
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosis.
    Barseghyan H; Tang W; Wang RT; Almalvez M; Segura E; Bramble MS; Lipson A; Douine ED; Lee H; Délot EC; Nelson SF; Vilain E
    Genome Med; 2017 Oct; 9(1):90. PubMed ID: 29070057
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Next-Generation Sequencing: An Emerging Tool for Drug Designing.
    Tripathi P; Singh J; Lal JA; Tripathi V
    Curr Pharm Des; 2019; 25(31):3350-3357. PubMed ID: 31544713
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A phylogenetic framework facilitates Y-STR variant discovery and classification via massively parallel sequencing.
    Huszar TI; Jobling MA; Wetton JH
    Forensic Sci Int Genet; 2018 Jul; 35():97-106. PubMed ID: 29679929
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Evaluation of the precision ID mtDNA whole genome panel on two massively parallel sequencing systems.
    Woerner AE; Ambers A; Wendt FR; King JL; Moura-Neto RS; Silva R; Budowle B
    Forensic Sci Int Genet; 2018 Sep; 36():213-224. PubMed ID: 30059903
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. SNP frequency estimation using massively parallel sequencing of pooled DNA.
    Ingman M; Gyllensten U
    Eur J Hum Genet; 2009 Mar; 17(3):383-6. PubMed ID: 18854868
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Advantages and limitations of next-generation sequencing technologies: a comparison of electrophoresis and non-electrophoresis methods.
    Hert DG; Fredlake CP; Barron AE
    Electrophoresis; 2008 Dec; 29(23):4618-26. PubMed ID: 19053153
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Whole-genome sequencing and variant discovery in C. elegans.
    Hillier LW; Marth GT; Quinlan AR; Dooling D; Fewell G; Barnett D; Fox P; Glasscock JI; Hickenbotham M; Huang W; Magrini VJ; Richt RJ; Sander SN; Stewart DA; Stromberg M; Tsung EF; Wylie T; Schedl T; Wilson RK; Mardis ER
    Nat Methods; 2008 Feb; 5(2):183-8. PubMed ID: 18204455
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Methods for genomic partitioning.
    Turner EH; Ng SB; Nickerson DA; Shendure J
    Annu Rev Genomics Hum Genet; 2009; 10():263-84. PubMed ID: 19630561
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Massively parallel sequencing for diagnosing clinically and genetically heterogeneous disorders.
    Zhang VW
    Per Med; 2013 Aug; 10(6):613-619. PubMed ID: 29776194
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of Disease Susceptibility Alleles in the Next Generation Sequencing Era.
    DiStefano JK; Kingsley CB
    Methods Mol Biol; 2018; 1706():3-16. PubMed ID: 29423790
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ultrasensitive single-genome sequencing: accurate, targeted, next generation sequencing of HIV-1 RNA.
    Boltz VF; Rausch J; Shao W; Hattori J; Luke B; Maldarelli F; Mellors JW; Kearney MF; Coffin JM
    Retrovirology; 2016 Dec; 13(1):87. PubMed ID: 27998286
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.