Automated NGS Workflow in Clinical Routine Cancer Diagnostics

被引:0
|
作者
Kifle, S. [1 ]
Herold, T. [2 ,3 ]
机构
[1] Tecan, Mannedorf, Switzerland
[2] Inst Pathol, Essen, Germany
[3] Inst Neuropathol, Mol Pathol, Essen, Germany
来源
JOURNAL OF MOLECULAR DIAGNOSTICS | 2020年 / 22卷 / 05期
关键词
D O I
暂无
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
10-P17
引用
收藏
页码:S99 / S99
页数:1
相关论文
共 50 条
  • [1] Automated Workflow for Somatic and Germline Next Generation Sequencing Analysis in Routine Clinical Cancer Diagnostics
    Muscarella, Lucia Anna
    Fabrizio, Federico Pio
    De Bonis, Maria
    Mancini, Maria Teresa
    Balsamo, Teresa
    Graziano, Paolo
    Centra, Flavia
    Sparaneo, Angelo
    Trombetta, Domenico
    Bonfitto, Antonio
    Scagliusi, Vito
    Larizza, Pietro
    Capoluongo, Ettore Domenico
    Fazio, Vito Michele
    CANCERS, 2019, 11 (11)
  • [2] A RNA workflow designed for routine clinical diagnostics
    Jemt, A.
    Eisfeldt, J.
    Lindstrand, A.
    Wedell, A.
    Stranneheim, H.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1659 - 1659
  • [3] Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework
    Tenedini, Elena
    Celestini, Fabio
    Iapicca, Pierluigi
    Marino, Marco
    Castellano, Sara
    Artuso, Lucia
    Biagiarelli, Fiammetta
    Cortesi, Laura
    Toss, Angela
    Barbieri, Elena
    Roncucci, Luca
    Pedroni, Monica
    Manfredini, Rossella
    Luppi, Mario
    Trenti, Tommaso
    Tagliafico, Enrico
    DIAGNOSIS, 2022, 9 (01) : 115 - 122
  • [4] PipeMAGI: an integrated and validated workflow for analysis of NGS data for clinical diagnostics
    Marceddu, G.
    Dallavilla, T.
    Guerri, G.
    Manara, E.
    Chiurazzi, P.
    Bertelli, M.
    EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, 2019, 23 (15) : 6753 - 6765
  • [5] Mosaicism in germline NGS diagnostics - Findings from routine diagnostics
    Voigt, Christin
    Froehlich, Christine
    Chatelain, Philippe
    Gabriel, Heinz
    Biskup, Saskia
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 603 - 603
  • [6] Implementation of a Comprehensive NGS Workflow as an Integrated Solution for Clinical Cancer Diagnosis
    Lupo, S.
    Smith, T.
    Akkari, Y.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2017, 19 (02): : S49 - S49
  • [7] Unifying NGS Workflows: A Modularized Automated Approach for Streamlining Clinical Molecular Diagnostics Laboratories
    Lucas, F. A. San
    Pelicano, H.
    Gascoyne, J.
    Mercado, J.
    Ninan, S.
    Ozenci, J.
    Duose, D.
    Yang, R.
    Routbort, M.
    Patel, K.
    Roy, S.
    Wistuba, I.
    Luthra, R.
    Medeiros, J.
    Alvarez, H.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2023, 25 (06): : S79 - S79
  • [8] The evaluation of a new NGS system (GeneReader NGS System) in clinical use of cancer diagnostics: The first report
    Bisgin, A.
    Sonmezler, O.
    Boga, I.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 660 - 660
  • [9] Challenges in the introduction of next-generation sequencing (NGS) for diagnostics of myeloid malignancies into clinical routine use
    Ulrike Bacher
    Evgenii Shumilov
    Johanna Flach
    Naomi Porret
    Raphael Joncourt
    Gertrud Wiedemann
    Martin Fiedler
    Urban Novak
    Ursula Amstutz
    Thomas Pabst
    Blood Cancer Journal, 8
  • [10] Challenges in the introduction of next-generation sequencing (NGS) for diagnostics of myeloid malignancies into clinical routine use
    Bacher, Ulrike
    Shumilov, Evgenii
    Flach, Johanna
    Porret, Naomi
    Joncourt, Raphael
    Wiedemann, Gertrud
    Fiedler, Martin
    Novak, Urban
    Amstutz, Ursula
    Pabst, Thomas
    BLOOD CANCER JOURNAL, 2018, 8