BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

395 related articles for article (PubMed ID: 24447136)

  • 1. AG-NGS: a powerful and user-friendly computing application for the semi-automated preparation of next-generation sequencing libraries using open liquid handling platforms.
    Callejas S; Álvarez R; Benguria A; Dopazo A
    Biotechniques; 2014 Jan; 56(1):28-35. PubMed ID: 24447136
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical application of amplicon-based next-generation sequencing in cancer.
    Chang F; Li MM
    Cancer Genet; 2013 Dec; 206(12):413-9. PubMed ID: 24332266
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fluorescent amplification for next generation sequencing (FA-NGS) library preparation.
    Chiniquy J; Garber ME; Mukhopadhyay A; Hillson NJ
    BMC Genomics; 2020 Jan; 21(1):85. PubMed ID: 31992180
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Library preparation methods for next-generation sequencing: tone down the bias.
    van Dijk EL; Jaszczyszyn Y; Thermes C
    Exp Cell Res; 2014 Mar; 322(1):12-20. PubMed ID: 24440557
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. SeqAssist: a novel toolkit for preliminary analysis of next-generation sequencing data.
    Peng Y; Maxwell AS; Barker ND; Laird JG; Kennedy AJ; Wang N; Zhang C; Gong P
    BMC Bioinformatics; 2014; 15 Suppl 11(Suppl 11):S10. PubMed ID: 25349885
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Next-generation sequencing (NGS) in the microbiological world: How to make the most of your money.
    Vincent AT; Derome N; Boyle B; Culley AI; Charette SJ
    J Microbiol Methods; 2017 Jul; 138():60-71. PubMed ID: 26995332
    [TBL] [Abstract][Full Text] [Related]  

  • 8. HLA typing by next-generation sequencing - getting closer to reality.
    Gabriel C; Fürst D; Faé I; Wenda S; Zollikofer C; Mytilineos J; Fischer GF
    Tissue Antigens; 2014 Feb; 83(2):65-75. PubMed ID: 24447174
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Setting up next-generation sequencing in the medical laboratory.
    Yu B
    Methods Mol Biol; 2014; 1168():195-206. PubMed ID: 24870137
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A robust and cost-effective approach to sequence and analyze complete genomes of small RNA viruses.
    Dimitrov KM; Sharma P; Volkening JD; Goraichuk IV; Wajid A; Rehmani SF; Basharat A; Shittu I; Joannis TM; Miller PJ; Afonso CL
    Virol J; 2017 Apr; 14(1):72. PubMed ID: 28388925
    [TBL] [Abstract][Full Text] [Related]  

  • 11. NGS-QCbox and Raspberry for Parallel, Automated and Rapid Quality Control Analysis of Large-Scale Next Generation Sequencing (Illumina) Data.
    Katta MA; Khan AW; Doddamani D; Thudi M; Varshney RK
    PLoS One; 2015; 10(10):e0139868. PubMed ID: 26460497
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Automated digital microfluidic sample preparation for next-generation DNA sequencing.
    Kim H; Bartsch MS; Renzi RF; He J; Van de Vreugde JL; Claudnic MR; Patel KD
    J Lab Autom; 2011 Dec; 16(6):405-14. PubMed ID: 22093297
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CANEapp: a user-friendly application for automated next generation transcriptomic data analysis.
    Velmeshev D; Lally P; Magistri M; Faghihi MA
    BMC Genomics; 2016 Jan; 17():49. PubMed ID: 26758513
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ICO amplicon NGS data analysis: a Web tool for variant detection in common high-risk hereditary cancer genes analyzed by amplicon GS Junior next-generation sequencing.
    Lopez-Doriga A; Feliubadaló L; Menéndez M; Lopez-Doriga S; Morón-Duran FD; del Valle J; Tornero E; Montes E; Cuesta R; Campos O; Gómez C; Pineda M; González S; Moreno V; Capellá G; Lázaro C
    Hum Mutat; 2014 Mar; 35(3):271-7. PubMed ID: 24227591
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SMITH: a LIMS for handling next-generation sequencing workflows.
    Venco F; Vaskin Y; Ceol A; Muller H
    BMC Bioinformatics; 2014; 15 Suppl 14(Suppl 14):S3. PubMed ID: 25471934
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recent novel approaches for population genomics data analysis.
    Andrews KR; Luikart G
    Mol Ecol; 2014 Apr; 23(7):1661-7. PubMed ID: 24495199
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Next-generation sequencing library construction on a surface.
    Feng K; Costa J; Edwards JS
    BMC Genomics; 2018 May; 19(1):416. PubMed ID: 29848309
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework.
    Tenedini E; Celestini F; Iapicca P; Marino M; Castellano S; Artuso L; Biagiarelli F; Cortesi L; Toss A; Barbieri E; Roncucci L; Pedroni M; Manfredini R; Luppi M; Trenti T; Tagliafico E
    Diagnosis (Berl); 2021 Jun; 9(1):115-122. PubMed ID: 34142509
    [TBL] [Abstract][Full Text] [Related]  

  • 19. QuickNGS elevates Next-Generation Sequencing data analysis to a new level of automation.
    Wagle P; Nikolić M; Frommolt P
    BMC Genomics; 2015 Jul; 16(1):487. PubMed ID: 26126663
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Leveraging the fundamentals of heat transfer and fluid mechanics in microscale geometries for automated next-generation sequencing library preparation.
    Ott O; Tolppi S; Figueroa-Cruz J; Myagmar K; Unurbuyan K; Tripathi A
    Sci Rep; 2024 May; 14(1):12564. PubMed ID: 38822053
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.