BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 19317667)

  • 1. Method for improving sequence coverage uniformity of targeted genomic intervals amplified by LR-PCR using Illumina GA sequencing-by-synthesis technology.
    Harismendy O; Frazer K
    Biotechniques; 2009 Mar; 46(3):229-31. PubMed ID: 19317667
    [TBL] [Abstract][Full Text] [Related]  

  • 2. THOR: targeted high-throughput ortholog reconstructor.
    Bainbridge MN; Warren RL; He A; Bilenky M; Robertson AG; Jones SJ
    Bioinformatics; 2007 Oct; 23(19):2622-4. PubMed ID: 17038343
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SNP discovery performance of two second-generation sequencing platforms in the NOD2 gene region.
    Melum E; May S; Schilhabel MB; Thomsen I; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    Hum Mutat; 2010 Jul; 31(7):875-85. PubMed ID: 20506538
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Using 454 technology for long-PCR based sequencing of the complete mitochondrial genome from single Haemonchus contortus (Nematoda).
    Jex AR; Hu M; Littlewood DT; Waeschenbach A; Gasser RB
    BMC Genomics; 2008 Jan; 9():11. PubMed ID: 18190685
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Primer design for PCR and sequencing in high-throughput analysis of SNPs.
    Vieux EF; Kwok PY; Miller RD
    Biotechniques; 2002 Jun; Suppl():28-30, 32. PubMed ID: 12083394
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Long PCR Product Sequencing (LoPPS): a shotgun-based approach to sequence long PCR products.
    Emonet SF; Grard G; Brisbarre NM; Moureau GN; Temmam S; Charrel RN; de Lamballerie X
    Nat Protoc; 2007; 2(2):340-6. PubMed ID: 17406595
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fast, cost-effective development of species-specific microsatellite markers by genomic sequencing.
    Abdelkrim J; Robertson B; Stanton JA; Gemmell N
    Biotechniques; 2009 Mar; 46(3):185-92. PubMed ID: 19317661
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Microsatellite discovery by deep sequencing of enriched genomic libraries.
    Santana Q; Coetzee M; Steenkamp E; Mlonyeni O; Hammond G; Wingfield M; Wingfield B
    Biotechniques; 2009 Mar; 46(3):217-23. PubMed ID: 19317665
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 96-plex molecular barcoding for the Illumina Genome Analyzer.
    Kozarewa I; Turner DJ
    Methods Mol Biol; 2011; 733():279-98. PubMed ID: 21431778
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Target-enrichment through amplification of hairpin-ligated universal targets for next-generation sequencing analysis.
    Singh P; Nayak R; Kwon YM
    Methods Mol Biol; 2011; 733():267-78. PubMed ID: 21431777
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An adapter ligation-mediated PCR method for high-throughput mapping of T-DNA inserts in the Arabidopsis genome.
    O'Malley RC; Alonso JM; Kim CJ; Leisse TJ; Ecker JR
    Nat Protoc; 2007; 2(11):2910-7. PubMed ID: 18007627
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Probabilistic base calling of Solexa sequencing data.
    Rougemont J; Amzallag A; Iseli C; Farinelli L; Xenarios I; Naef F
    BMC Bioinformatics; 2008 Oct; 9():431. PubMed ID: 18851737
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Preparing a re-sequencing DNA library of 2 cancer candidate genes using the ligation-by-amplification protocol by two PCR reactions.
    Su Y; Lin L; Tian G; Chen C; Liu T; Xu X; Qi X; Zhang X; Yang H
    Sci China C Life Sci; 2009 May; 52(5):483-91. PubMed ID: 19471873
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bar-coded, multiplexed sequencing of targeted DNA regions using the Illumina Genome Analyzer.
    Szelinger S; Kurdoglu A; Craig DW
    Methods Mol Biol; 2011; 700():89-104. PubMed ID: 21204029
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Applications of next-generation sequencing technologies in functional genomics.
    Morozova O; Marra MA
    Genomics; 2008 Nov; 92(5):255-64. PubMed ID: 18703132
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapid quantification of DNA libraries for next-generation sequencing.
    Buehler B; Hogrefe HH; Scott G; Ravi H; Pabón-Peña C; O'Brien S; Formosa R; Happe S
    Methods; 2010 Apr; 50(4):S15-8. PubMed ID: 20215015
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cloneless genomic DNA analysis: an efficient and simple methods for de novo genomic sequencing projects and gap filling.
    Nguyen G; Bukanov N; Oshimura M; Smith CL
    Biomol Eng; 2005 Feb; 21(6):135-44. PubMed ID: 15748687
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of microsatellites from an extinct moa species using high-throughput (454) sequence data.
    Allentoft M; Schuster SC; Holdaway R; Hale M; McLay E; Oskam C; Gilbert MT; Spencer P; Willerslev E; Bunce M
    Biotechniques; 2009 Mar; 46(3):195-200. PubMed ID: 19317662
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Targeted high throughput sequencing of a cancer-related exome subset by specific sequence capture with a fully automated microarray platform.
    Summerer D; Schracke N; Wu H; Cheng Y; Bau S; Stähler CF; Stähler PF; Beier M
    Genomics; 2010 Apr; 95(4):241-6. PubMed ID: 20138981
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Enabling technologies of genomic-scale sequence enrichment for targeted high-throughput sequencing.
    Summerer D
    Genomics; 2009 Dec; 94(6):363-8. PubMed ID: 19720138
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.