Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing

被引:263
|
作者
Thomas, Roman K.
Nickerson, Elizabeth
Simons, Jan F.
Janne, Pasi A.
Tengs, Torstein
Yuza, Yuki
Garraway, Levi A.
LaFramboise, Thomas
Lee, Jeffrey C.
Shah, Kinjal
O'Neill, Keith
Sasaki, Hidefumi
Lindeman, Neal
Wong, Kwok-Kin
Borras, Ana M.
Gutmann, Edward J.
Dragnev, Konstantin H.
DeBiasi, Ralph
Chen, Tzu-Hsiu
Glatt, Karen A.
Greulich, Heidi
Desany, Brian
Lubeski, Christine K.
Brockman, William
Alvarez, Pablo
Hutchison, Stephen K.
Leamon, J. H.
Ronan, Michael T.
Turenchalk, Gregory S.
Egholm, Michael
Sellers, William R.
Rothberg, Jonathan M.
Meyerson, Matthew
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] MIT, Broad Inst, Cambridge, MA 02142 USA
[3] Harvard Univ, Cambridge Ctr 7, Cambridge, MA 02142 USA
[4] Dana Farber Canc Inst, Melanoma Program Med Oncol, Boston, MA 02115 USA
[5] Nagoya City Univ, Sch Med, Dept Surg 2, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[6] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[7] Dana Farber Canc Inst, Translat Res Lab, Boston, MA 02115 USA
[8] Dartmouth Hitchcock Med Ctr, Dept Pathol, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
[9] Dartmouth Hitchcock Med Ctr, Dept Med, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
[10] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[11] Dana Farber Canc Inst, Ctr Canc Genome Discovery, Boston, MA 02115 USA
关键词
D O I
10.1038/nm1437
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sensitivity of conventional DNA sequencing in tumor biopsies is limited by stromal contamination and by genetic heterogeneity within the cancer. Here, we show that microreactor-based pyrosequencing can detect rare cancer-associated sequence variations by independent and parallel sampling of multiple representatives of a given DNA fragment. This technology can thereby facilitate accurate molecular diagnosis of heterogeneous cancer specimens and enable patient selection for targeted cancer therapies.
引用
收藏
页码:852 / 855
页数:4
相关论文
共 50 条
  • [31] Detection of Diverse Mutational Signatures using Targeted Massively Parallel Sequencing
    Nowak, Jonathan A.
    Schmidt, Ryan
    Posada, Jessica
    Dong, Fei
    Frieden, Alexander
    Shivdasani, Priyanka
    Bialic, Leah
    Ducar, Matthew D.
    Lindeman, Neal
    MacConaill, Laura E.
    Kuo, Frank
    Sholl, Lynette
    MODERN PATHOLOGY, 2018, 31 : 705 - 705
  • [32] Detection of Diverse Mutational Signatures using Targeted Massively Parallel Sequencing
    Nowak, Jonathan A.
    Schmidt, Ryan
    Posada, Jessica
    Dong, Fei
    Frieden, Alexander
    Shivdasani, Priyanka
    Bialic, Leah
    Ducar, Matthew D.
    Lindeman, Neal
    MacConaill, Laura E.
    Kuo, Frank
    Sholl, Lynette
    LABORATORY INVESTIGATION, 2018, 98 : 705 - 705
  • [33] A new method for mtDNA deletion detection using massively parallel sequencing
    Penttila, S.
    Suominen, T.
    Lehtinen, S.
    Jokela, M.
    Palmio, J.
    Udd, B.
    NEUROMUSCULAR DISORDERS, 2019, 29 : S152 - S152
  • [34] VarScan: variant detection in massively parallel sequencing of individual and pooled samples
    Koboldt, Daniel C.
    Chen, Ken
    Wylie, Todd
    Larson, David E.
    McLellan, Michael D.
    Mardis, Elaine R.
    Weinstock, George M.
    Wilson, Richard K.
    Ding, Li
    BIOINFORMATICS, 2009, 25 (17) : 2283 - 2285
  • [35] Comprehensive detection of chromosomal translocations in lymphoproliferative disorders by massively parallel sequencing
    Philippe Szankasi
    Ashini Bolia
    Michael Liew
    Jonathan A. Schumacher
    Elaine P. S. Gee
    Anna P. Matynia
    K. David Li
    Jay L. Patel
    Xinjie Xu
    Mohamed E. Salama
    Todd W. Kelley
    Journal of Hematopathology, 2019, 12 : 121 - 133
  • [36] The "Are You You" Assay (RUU Assay): A Sensitive Method for the Detection of Sample Switching in a Clinical Massively Parallel Sequencing Laboratory
    Meltzer, B. W.
    Devaney, J. M.
    Cusmano-Ozog, K. P.
    Campos, J. M.
    Hofherr, S. E.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2015, 17 (06): : 754 - 754
  • [37] MASSIVELY PARALLEL SEQUENCING ANALYSIS OF UTERINE PECOMAS REVEALS A HETEROGENEOUS REPERTOIRE OF GENETIC ALTERATIONS
    Murali, R.
    Lee, J. Y.
    Selenica, P.
    Hensley, M. L.
    Conlon, N.
    Chiang, S.
    Soslow, R. A.
    Weigelt, B.
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2017, 27 : 1986 - 1986
  • [38] Analysis of mtDNA multiple deletions in 209 muscle specimens using massively parallel sequencing (MPS)
    Li, Fang-Yuan
    Tian, Xia
    Milone, Margherita
    Cui, Hong
    Zhang, Victor Wei
    Wong, Lee-Jun
    MITOCHONDRION, 2013, 13 (06) : 932 - 932
  • [39] Analysis of luminal-type breast cancer by massively parallel sequencing
    Ellis, Matthew J.
    Ding, Li
    Shen, Dong
    Wallis, John
    Suman, Vera
    Luo, Jingqin
    Tao, Yu
    Hoog, Jeremy
    Davies, Sherri
    Lin, Li
    Perou, Charles
    Van Tine, Brian
    Bose, Ron
    Chang, Li Wei
    Chen, Ken
    Ota, David
    Watson, Mark
    Wilson, Richard
    Hunt, Kelly
    Mardis, Elaine
    CANCER RESEARCH, 2011, 71
  • [40] Clinical application of massively parallel sequencing on chromosomal abnormalities detection of human blastocysts
    Li, J.
    Yin, X. Y.
    Tan, K.
    Tan, Y. Q.
    Chen, F.
    Zhang, L. E. I.
    Lin, G.
    Jiang, H.
    Wang, W.
    HUMAN REPRODUCTION, 2013, 28 : 26 - 26