Application of Targeted Next-generation Sequencing, TruSeq Custom Amplicon Assay for Molecular Pathology Diagnostics on Formalin-fixed and Paraffin-embedded Samples

被引:7
作者
Csernak, Erzsebet [1 ]
Molnar, Janos [2 ]
Tusnady, Gabor E. [2 ]
Toth, Erika [1 ]
机构
[1] Natl Inst Oncol, Dept Surg & Mol Pathol, Rath Gy U 7-9, H-1122 Budapest, Hungary
[2] Hungarian Acad Sci, Inst Enzymol, Momentum Membrane Prot Bioinformat Res Grp, Res Ctr Nat Sci, Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
massively parallel sequencing; TruSeq Custom Amplicon assay; molecular pathology; FFPE tissue;
D O I
10.1097/PAI.0000000000000325
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The implementation of targeted therapies revolutionized oncology. As the number of new oncogenic driver mutations, which provide molecular targets for prediction of effective and selective therapies, is increasing, the implementation of fast and reliable methods by molecular pathology labs is very important. Here we report our results with TruSeq Custom Amplicon assay performed on formalin-fixed and paraffin-embedded material. The oligo capture probes targeted the hotspot regions of 10 well-known oncogenes linked to clinical diagnosis and treatment of lung and colorectal adenocarcinomas, melanomas, and gastrointestinal stromal tumors. Fifteen previously genotyped formalin-fixed and paraffin-embedded DNA samples from different tumor types were selected for massively parallel sequencing. A bioinformatics pipeline was developed to identify high-quality variants and remove sequence artifacts. With the exception of 1 sample, which was of lower quality than the others, relevant mutations corresponding to tumor types could be reliable detected by the developed bioinformatical pipeline. This study indicates that the application of TruSeq Custom Amplicon assay is a promising tool in molecular pathology diagnostics, but it is important to standardize sample processing (including fixation, isolation procedure, sample selection based on quality assessment, and rigorous variant calling) to achieve the highest success rate and avoid false results.
引用
收藏
页码:460 / 466
页数:7
相关论文
共 12 条
  • [1] Ensembl 2014
    Flicek, Paul
    Amode, M. Ridwan
    Barrell, Daniel
    Beal, Kathryn
    Billis, Konstantinos
    Brent, Simon
    Carvalho-Silva, Denise
    Clapham, Peter
    Coates, Guy
    Fitzgerald, Stephen
    Gil, Laurent
    Giron, Carlos Garcia
    Gordon, Leo
    Hourlier, Thibaut
    Hunt, Sarah
    Johnson, Nathan
    Juettemann, Thomas
    Kaehaeri, Andreas K.
    Keenan, Stephen
    Kulesha, Eugene
    Martin, Fergal J.
    Maurel, Thomas
    McLaren, William M.
    Murphy, Daniel N.
    Nag, Rishi
    Overduin, Bert
    Pignatelli, Miguel
    Pritchard, Bethan
    Pritchard, Emily
    Riat, Harpreet S.
    Ruffier, Magali
    Sheppard, Daniel
    Taylor, Kieron
    Thormann, Anja
    Trevanion, Stephen J.
    Vullo, Alessandro
    Wilder, Steven P.
    Wilson, Mark
    Zadissa, Amonida
    Aken, Bronwen L.
    Birney, Ewan
    Cunningham, Fiona
    Harrow, Jennifer
    Herrero, Javier
    Hubbard, Tim J. P.
    Kinsella, Rhoda
    Muffato, Matthieu
    Parker, Anne
    Spudich, Giulietta
    Yates, Andy
    [J]. NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) : D749 - D755
  • [2] Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
    Hedegaard, Jakob
    Thorsen, Kasper
    Lund, Mette Katrine
    Hein, Anne-Mette K.
    Hamilton-Dutoit, Stephen Jacques
    Vang, Soren
    Nordentoft, Iver
    Birkenkamp-Demtroder, Karin
    Kruhoffer, Mogens
    Hager, Henrik
    Knudsen, Bjarne
    Andersen, Claus Lindbjerg
    Sorensen, Karina Dalsgaard
    Pedersen, Jakob Skou
    Orntoft, Torben Falck
    Dyrskjot, Lars
    [J]. PLOS ONE, 2014, 9 (05):
  • [3] Linear amplification for deep sequencing
    Hoeijmakers, Wieteke A. M.
    Bartfai, Richard
    Francoijs, Kees-Jan
    Stunnenberg, Hendrik G.
    [J]. NATURE PROTOCOLS, 2011, 6 (07) : 1026 - 1036
  • [4] Targeted high throughput sequencing in clinical cancer Settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity
    Kerick, Martin
    Isau, Melanie
    Timmermann, Bernd
    Sueltmann, Holger
    Herwig, Ralf
    Krobitsch, Sylvia
    Schaefer, Georg
    Verdorfer, Irmgard
    Bartsch, Georg
    Klocker, Helmut
    Lehrach, Hans
    Schweiger, Michal R.
    [J]. BMC MEDICAL GENOMICS, 2011, 4
  • [5] Li H, 2009, BIOINFORMATICS, V25, P1094, DOI [10.1093/bioinformatics/btp100, 10.1093/bioinformatics/btp324]
  • [6] Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
    McLaren, William
    Pritchard, Bethan
    Rios, Daniel
    Chen, Yuan
    Flicek, Paul
    Cunningham, Fiona
    [J]. BIOINFORMATICS, 2010, 26 (16) : 2069 - 2070
  • [7] Meldrum Cliff, 2011, Clin Biochem Rev, V32, P177
  • [8] Integrative genomics viewer
    Robinson, James T.
    Thorvaldsdottir, Helga
    Winckler, Wendy
    Guttman, Mitchell
    Lander, Eric S.
    Getz, Gad
    Mesirov, Jill P.
    [J]. NATURE BIOTECHNOLOGY, 2011, 29 (01) : 24 - 26
  • [9] A high frequency of sequence alterations is due to formalin fixation of archival specimens
    Williams, C
    Pontén, F
    Moberg, C
    Söderkvist, P
    Uhlén, M
    Pontén, J
    Sitbon, G
    Lundeberg, J
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (05) : 1467 - 1471
  • [10] Targeted-capture massively-parallel sequencing enables robust detection of clinically informative mutations from formalin-fixed tumours
    Wong, Stephen Q.
    Li, Jason
    Salemi, Renato
    Sheppard, Karen E.
    Do, Hongdo
    Tothill, Richard W.
    McArthur, Grant A.
    Dobrovic, Alexander
    [J]. SCIENTIFIC REPORTS, 2013, 3