BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 21431775)

  • 1. Preparation of next-generation sequencing libraries using Nextera™ technology: simultaneous DNA fragmentation and adaptor tagging by in vitro transposition.
    Caruccio N
    Methods Mol Biol; 2011; 733():241-55. PubMed ID: 21431775
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. In vitro double transposition for DNA identification.
    Heredia NJ; Beer NR; Hara CA; Hiddessen AL; Bailey CG
    Anal Biochem; 2010 Apr; 399(1):78-83. PubMed ID: 19944058
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Illumina sequencing library preparation for highly multiplexed target capture and sequencing.
    Meyer M; Kircher M
    Cold Spring Harb Protoc; 2010 Jun; 2010(6):pdb.prot5448. PubMed ID: 20516186
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Amplification-free library preparation for paired-end Illumina sequencing.
    Kozarewa I; Turner DJ
    Methods Mol Biol; 2011; 733():257-66. PubMed ID: 21431776
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Generating barcoded libraries for multiplex high-throughput sequencing.
    Knapp M; Stiller M; Meyer M
    Methods Mol Biol; 2012; 840():155-70. PubMed ID: 22237533
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Preparation of next-generation sequencing libraries from damaged DNA.
    Briggs AW; Heyn P
    Methods Mol Biol; 2012; 840():143-54. PubMed ID: 22237532
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Parallel tagged sequencing on the 454 platform.
    Meyer M; Stenzel U; Hofreiter M
    Nat Protoc; 2008; 3(2):267-78. PubMed ID: 18274529
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microfluidics for the upstream pipeline of DNA sequencing--a worthy application?
    Coupland P
    Lab Chip; 2010 Mar; 10(5):544-7. PubMed ID: 20162226
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Improved transposon-based library preparation for the Ion Torrent platform.
    Gorbacheva T; Quispe-Tintaya W; Popov VN; Vijg J; Maslov AY
    Biotechniques; 2015 Apr; 58(4):200-2. PubMed ID: 25861933
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Preparation of a phage DNA fragment library for whole genome shotgun sequencing.
    Summer EJ
    Methods Mol Biol; 2009; 502():27-46. PubMed ID: 19082550
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An efficient DNA sequencing strategy based on the bacteriophage mu in vitro DNA transposition reaction.
    Haapa S; Suomalainen S; Eerikäinen S; Airaksinen M; Paulin L; Savilahti H
    Genome Res; 1999 Mar; 9(3):308-15. PubMed ID: 10077537
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Roche genome sequencer FLX based high-throughput sequencing of ancient DNA.
    Alquezar-Planas DE; Fordyce SL
    Methods Mol Biol; 2012; 888():109-18. PubMed ID: 22665278
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Quality control of next-generation sequencing library through an integrative digital microfluidic platform.
    Thaitrong N; Kim H; Renzi RF; Bartsch MS; Meagher RJ; Patel KD
    Electrophoresis; 2012 Dec; 33(23):3506-13. PubMed ID: 23135807
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Bead-linked transposomes enable a normalization-free workflow for NGS library preparation.
    Bruinsma S; Burgess J; Schlingman D; Czyz A; Morrell N; Ballenger C; Meinholz H; Brady L; Khanna A; Freeberg L; Jackson RG; Mathonet P; Verity SC; Slatter AF; Golshani R; Grunenwald H; Schroth GP; Gormley NA
    BMC Genomics; 2018 Oct; 19(1):722. PubMed ID: 30285621
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Preparation of fragment libraries for next-generation sequencing on the applied biosystems SOLiD platform.
    Yegnasubramanian S
    Methods Enzymol; 2013; 529():185-200. PubMed ID: 24011046
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.