-
1
-
-
79960597679
-
An integrated semiconductor device enabling non-optical genome sequencing
-
Rothberg JM, Hinz W, Rearick TM, et al. An integrated semiconductor device enabling non-optical genome sequencing. Nature. 2011;475:348–52.
-
(2011)
Nature
, vol.475
, pp. 348-352
-
-
Rothberg, J.M.1
Hinz, W.2
Rearick, T.M.3
-
2
-
-
84869429716
-
Assuring the quality of next-generation sequencing in clinical laboratory practice
-
Gargis AS, Kalman L, Berry MW, et al. Assuring the quality of next-generation sequencing in clinical laboratory practice. Nat Biotechnol. 2012;30:1033–6.
-
(2012)
Nat Biotechnol
, vol.30
, pp. 1033-1036
-
-
Gargis, A.S.1
Kalman, L.2
Berry, M.W.3
-
3
-
-
84875490185
-
Cancer genome landscapes
-
Vogelstein B, Velculescu VE, Zhou S, Diaz LA Jr, Kinzler KW. Cancer genome landscapes. Science. 2013;339:1546–58.
-
(2013)
Science
, vol.339
, pp. 1546-1558
-
-
Vogelstein, B.1
Velculescu, V.E.2
Zhou, S.3
Diaz, L.A.4
Kinzler, K.W.5
-
4
-
-
79951897927
-
Selecting systemic cancer therapy one patient at a time: Is there a role for molecular profiling of individual patients with advanced solid tumors?
-
Doroshow JH. Selecting systemic cancer therapy one patient at a time: is there a role for molecular profiling of individual patients with advanced solid tumors? J Clin Oncol. 2010;28(33):4869–71.
-
(2010)
J Clin Oncol
, vol.28
, Issue.33
, pp. 4869-4871
-
-
Doroshow, J.H.1
-
5
-
-
84877278637
-
Implementing personalized cancer genomics in clinical trials
-
Simon R, Roychowdhury S. Implementing personalized cancer genomics in clinical trials. Nat Rev Drug Discov. 2013;12(5):358–69.
-
(2013)
Nat Rev Drug Discov
, vol.12
, Issue.5
, pp. 358-369
-
-
Simon, R.1
Roychowdhury, S.2
-
6
-
-
84880206315
-
Clinical trials for precision oncology using next-generation sequencing
-
Simon R, Polley E. Clinical trials for precision oncology using next-generation sequencing. J Pers Med. 2013;10:485–95.
-
(2013)
J Pers Med
, vol.10
, pp. 485-495
-
-
Simon, R.1
Polley, E.2
-
7
-
-
84873093569
-
Feasibility of real time next generation sequencing of cancer genes linked to drug response: Results from a clinical trial
-
Tran B, Brown AM, Bedard PL, et al. Feasibility of real time next generation sequencing of cancer genes linked to drug response: results from a clinical trial. Int J Cancer. 2013;132(7):1547–55.
-
(2013)
Int J Cancer
, vol.132
, Issue.7
, pp. 1547-1555
-
-
Tran, B.1
Brown, A.M.2
Bedard, P.L.3
-
8
-
-
84925377660
-
Application of molecular profiling in clinical trials for advanced metastatic cancers
-
Kummar S, Williams PM, Lih CJ, et al. Application of molecular profiling in clinical trials for advanced metastatic cancers. J Natl Cancer Inst. 2015; 107(4):djv003.
-
(2015)
J Natl Cancer Inst
, vol.107
, Issue.4
-
-
Kummar, S.1
Williams, P.M.2
Lih, C.J.3
-
10
-
-
3843084078
-
The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website
-
Bamford S, Dawson E, Forbes S, et al. The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website. Br J Cancer. 2004;91(2):355–8.
-
(2004)
Br J Cancer
, vol.91
, Issue.2
, pp. 355-358
-
-
Bamford, S.1
Dawson, E.2
Forbes, S.3
-
11
-
-
84862506964
-
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso−3
-
Cingolani P, Platts A, Wang le L, et al. A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso−3. Fly (Austin). 2012;6(2):80–92.
-
(2012)
Fly (Austin)
, vol.6
, Issue.2
, pp. 80-92
-
-
Cingolani, P.1
Platts, A.2
Wang Le, L.3
-
12
-
-
0035026704
-
Predicting deleterious amino acid substitutions
-
Ng PC, Henikoff S. Predicting deleterious amino acid substitutions. Genome Res. 2001;11(5):863–74.
-
(2001)
Genome Res
, vol.11
, Issue.5
, pp. 863-874
-
-
Ng, P.C.1
Henikoff, S.2
-
13
-
-
84868343901
-
The human gene mutation database (HGMD) and its exploitation in the fields of personalized genomics and molecular evolution
-
Stenson PD, Ball EV, Mort M, Phillips AD, Shaw K, Cooper DN. The human gene mutation database (HGMD) and its exploitation in the fields of personalized genomics and molecular evolution. Curr Protoc Bioinformatics. 2012; Chapter 1:Unit1.13.
-
(2012)
Curr Protoc Bioinformatics
, vol.1
, Issue.13
-
-
Stenson, P.D.1
Ball, E.V.2
Mort, M.3
Phillips, A.D.4
Shaw, K.5
Cooper, D.N.6
-
15
-
-
84890328625
-
SeqReporter: Automating next-generation sequencing result interpretation and reporting workflow in a clinical Laboratory
-
Roy S, Burso MB, Wald A, Nikiforov YE, Nikiforova MN. SeqReporter: automating next-generation sequencing result interpretation and reporting workflow in a clinical Laboratory. J Mol Diagn. 2014;16:11–22.
-
(2014)
J Mol Diagn
, vol.16
, pp. 11-22
-
-
Roy, S.1
Burso, M.B.2
Wald, A.3
Nikiforov, Y.E.4
Nikiforova, M.N.5
-
16
-
-
84905642719
-
Bioinformatics for precision medicine in oncology: Principles and application to the SHIVA clinical trial
-
Servant N, Roméjon J, Gestraud P, et al. Bioinformatics for precision medicine in oncology: principles and application to the SHIVA clinical trial. Front Genet. 2014;5:152.
-
(2014)
Front Genet
, vol.5
, pp. 152
-
-
Servant, N.1
Roméjon, J.2
Gestraud, P.3
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