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
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