Molecular pathology of the lungs. New perspectives by next generation sequencing

被引:4
|
作者
Vollbrecht, C. [1 ]
Koenig, K. [1 ]
Heukamp, L. [1 ]
Buettner, R. [1 ]
Odenthal, M. [1 ]
机构
[1] Univ Klin Koln, Inst Pathol, D-50924 Cologne, Germany
来源
PATHOLOGE | 2013年 / 34卷 / 01期
关键词
Parallel sequencing; Pyrosequencing; Semiconductor sequencing; Cancer panel; Personalized oncology; GROWTH-FACTOR RECEPTOR; TARGETED THERAPY; CANCER; MUTATIONS; EGFR;
D O I
10.1007/s00292-012-1704-7
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Lung cancer is one of the most frequent malignancies in the western world. Its frequent association with a wide spectrum of mutations in genes encoding various signal transducers that are often linked to therapy response, emphasizes the obvious need for improved, fast and highly efficient approaches in molecular pathology. Comprehensive analyses of the mutation status of progression and therapy relevant genes can be performed by the novel sequencing forms named next generation sequencing (NGS) providing extremely high capacities for ultra-deep sequence analyses. The 454 pyrosequencing method, the sequencing by synthesis and the semiconductor sequencing platform are now available for parallel sequencing approaches of multitudinous target genes linked to multiple tumor DNA applications. The "one molecule, one clone, one read" principle by the NGS approaches supplies not only information on allele frequencies and mutation rates but also has the advantage of a very sensitive detection of low frequency variants.
引用
收藏
页码:16 / 24
页数:9
相关论文
共 50 条
  • [21] Next Generation Sequencing of Ancient DNA: Requirements, Strategies and Perspectives
    Knapp, Michael
    Hofreiter, Michael
    GENES, 2010, 1 (02): : 227 - 243
  • [22] Next generation sequencing and a new era of medicine
    Casey, Graham
    Conti, David
    Haile, Robert
    Duggan, David
    GUT, 2013, 62 (06) : 920 - 932
  • [23] MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDAEMIAS BY NEXT GENERATION SEQUENCING
    Miranda, B.
    Alves, A. C. C.
    Bourbon, M.
    ATHEROSCLEROSIS, 2022, 355 : E230 - E231
  • [24] Importance of molecular genetics in the era of next generation sequencing
    Bullinger, L.
    ONCOLOGY RESEARCH AND TREATMENT, 2014, 37 : 20 - 20
  • [25] Next generation sequencing for molecular diagnosis of neuromuscular diseases
    Nasim Vasli
    Johann Böhm
    Stéphanie Le Gras
    Jean Muller
    Cécile Pizot
    Bernard Jost
    Andoni Echaniz-Laguna
    Vincent Laugel
    Christine Tranchant
    Rafaelle Bernard
    Frédéric Plewniak
    Serge Vicaire
    Nicolas Levy
    Jamel Chelly
    Jean-Louis Mandel
    Valérie Biancalana
    Jocelyn Laporte
    Acta Neuropathologica, 2012, 124 : 273 - 283
  • [26] Molecular Categorization of Glioblastomas Using Next Generation Sequencing
    Richard, Hope
    Harrison, Jason
    Dumur, Catherine
    Fuller, Christine
    LABORATORY INVESTIGATION, 2015, 95 : 436A - 436A
  • [27] Molecular characterization of cardiomyopathies: role of next generation sequencing
    Mastroianno, Sandra
    Leone, Maria Pia
    Palumbo, Pietro
    Castellana, Stefano
    Palumbo, Orazio
    Biagini, Tommaso
    Mazza, Tommaso
    Russo, Aldo
    Potenza, Domenico
    Castori, Marco
    Carella, Massimo
    Di Stolfo, Giuseppe
    EUROPEAN HEART JOURNAL SUPPLEMENTS, 2019, 21 (0J) : J180 - J181
  • [28] Next-generation sequencing applied to molecular diagnostics
    Natrajan, Rachael
    Reis-Filho, Jorge S.
    EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2011, 11 (04) : 425 - 444
  • [29] Next generation sequencing for molecular diagnosis of neuromuscular diseases
    Vasli, Nasim
    Boehm, Johann
    Le Gras, Stephanie
    Muller, Jean
    Pizot, Cecile
    Jost, Bernard
    Echaniz-Laguna, Andoni
    Laugel, Vincent
    Tranchant, Christine
    Bernard, Rafaelle
    Plewniak, Frederic
    Vicaire, Serge
    Levy, Nicolas
    Chelly, Jamel
    Mandel, Jean-Louis
    Biancalana, Valerie
    Laporte, Jocelyn
    ACTA NEUROPATHOLOGICA, 2012, 124 (02) : 273 - 283
  • [30] Molecular Categorization of Glioblastomas Using Next Generation Sequencing
    Richard, Hope
    Harrison, Jason
    Dumur, Catherine
    Fuller, Christine
    MODERN PATHOLOGY, 2015, 28 : 436A - 436A