-
1
-
-
84927171291
-
Targeting oncogenic drivers
-
Zhao Y, Adjei AA,. Targeting oncogenic drivers. Prog Tumor Res. 2014; 41: 1-14.
-
(2014)
Prog Tumor Res
, vol.41
, pp. 1-14
-
-
Zhao, Y.1
Adjei, A.A.2
-
2
-
-
84876240173
-
Targeting tyrosine kinases in cancer: The converging roles of cytopathology and molecular pathology in the era of genomic medicine
-
Dumur CI, Idowu MO, Powers CN,. Targeting tyrosine kinases in cancer: the converging roles of cytopathology and molecular pathology in the era of genomic medicine. Cancer Cytopathol. 2013; 121: 61-71.
-
(2013)
Cancer Cytopathol
, vol.121
, pp. 61-71
-
-
Dumur, C.I.1
Idowu, M.O.2
Powers, C.N.3
-
3
-
-
84899028356
-
Routine use of the Ion Torrent AmpliSeq Cancer Hotspot Panel for identification of clinically actionable somatic mutations
-
Tsongalis GJ, Peterson JD, de Abreu FB, et al., Routine use of the Ion Torrent AmpliSeq Cancer Hotspot Panel for identification of clinically actionable somatic mutations. Clin Chem Lab Med. 2014; 52: 707-714.
-
(2014)
Clin Chem Lab Med
, vol.52
, pp. 707-714
-
-
Tsongalis, G.J.1
Peterson, J.D.2
De Abreu, F.B.3
-
4
-
-
84896448861
-
A survey of tools for variant analysis of next-generation genome sequencing data
-
Pabinger S, Dander A, Fischer M, et al., A survey of tools for variant analysis of next-generation genome sequencing data. Brief Bioinform. 2014; 15: 256-278.
-
(2014)
Brief Bioinform
, vol.15
, pp. 256-278
-
-
Pabinger, S.1
Dander, A.2
Fischer, M.3
-
5
-
-
79960405019
-
The variant call format and VCFtools
-
Danecek P, Auton A, Abecasis G, et al., The variant call format and VCFtools. Bioinformatics. 2011; 27: 2156-2158.
-
(2011)
Bioinformatics
, vol.27
, pp. 2156-2158
-
-
Danecek, P.1
Auton, A.2
Abecasis, G.3
-
6
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
Abecasis GR, Auton A, Brooks LD, et al., An integrated map of genetic variation from 1,092 human genomes. Nature. 2012; 491: 56-65.
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
Abecasis, G.R.1
Auton, A.2
Brooks, L.D.3
-
7
-
-
84891837451
-
The Human Gene Mutation Database: Building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine
-
Stenson PD, Mort M, Ball EV, et al., The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine. Hum Genet. 2014; 133: 1-9.
-
(2014)
Hum Genet
, vol.133
, pp. 1-9
-
-
Stenson, P.D.1
Mort, M.2
Ball, E.V.3
-
9
-
-
84884759840
-
Databases of genomic variation and phenotypes: Existing resources and future needs
-
Johnston JJ, Biesecker LG,. Databases of genomic variation and phenotypes: existing resources and future needs. Hum Mol Genet. 2013; 22: R27-R31.
-
(2013)
Hum Mol Genet
, vol.22
, pp. R27-R31
-
-
Johnston, J.J.1
Biesecker, L.G.2
-
10
-
-
84891809093
-
ClinVar: Public archive of relationships among sequence variation and human phenotype
-
Landrum MJ, Lee JM, Riley GR, et al., ClinVar: public archive of relationships among sequence variation and human phenotype. Nucleic Acids Res. 2014; 42: D980-D985.
-
(2014)
Nucleic Acids Res
, vol.42
, pp. D980-D985
-
-
Landrum, M.J.1
Lee, J.M.2
Riley, G.R.3
-
11
-
-
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: 355-358.
-
(2004)
Br J Cancer
, vol.91
, pp. 355-358
-
-
Bamford, S.1
Dawson, E.2
Forbes, S.3
-
12
-
-
0033987736
-
Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
-
den Dunnen JT, Antonarakis SE,. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat. 2000; 15: 7-12.
-
(2000)
Hum Mutat
, vol.15
, pp. 7-12
-
-
Den Dunnen, J.T.1
Antonarakis, S.E.2
-
13
-
-
0027295745
-
A suggested nomenclature for designating mutations
-
Beaudet AL, Tsui LC,. A suggested nomenclature for designating mutations. Hum Mutat. 1993; 2: 245-248.
-
(1993)
Hum Mutat
, vol.2
, pp. 245-248
-
-
Beaudet, A.L.1
Tsui, L.C.2
-
14
-
-
0027339681
-
The designation of mutations
-
Beutler E,. The designation of mutations. Am J Hum Genet. 1993; 53: 783-785.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 783-785
-
-
Beutler, E.1
-
15
-
-
77955868835
-
Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations
-
Flanagan SE, Patch AM, Ellard S,. Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations. Genet Test Mol Biomarkers. 2010; 14: 533-537.
-
(2010)
Genet Test Mol Biomarkers
, vol.14
, pp. 533-537
-
-
Flanagan, S.E.1
Patch, A.M.2
Ellard, S.3
-
16
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, et al., A method and server for predicting damaging missense mutations. Nat Methods. 2010; 7: 248-249.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
-
17
-
-
84866002291
-
The cBio cancer genomics portal: An open platform for exploring multidimensional cancer genomics data
-
Cerami E, Gao J, Dogrusoz U, et al., The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. Cancer Discov. 2012; 2: 401-404.
-
(2012)
Cancer Discov
, vol.2
, pp. 401-404
-
-
Cerami, E.1
Gao, J.2
Dogrusoz, U.3
-
18
-
-
84875740314
-
Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal
-
Gao J, Aksoy BA, Dogrusoz U, et al., Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal. Sci Signal. 2013; 6: l1.
-
(2013)
Sci Signal
, vol.6
, pp. l1
-
-
Gao, J.1
Aksoy, B.A.2
Dogrusoz, U.3
-
19
-
-
84859169877
-
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
-
Barretina J, Caponigro G, Stransky N, et al., The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature. 2012; 483: 603-607.
-
(2012)
Nature
, vol.483
, pp. 603-607
-
-
Barretina, J.1
Caponigro, G.2
Stransky, N.3
-
20
-
-
84862601030
-
New approaches to targeted therapy in lung cancer
-
Pao W,. New approaches to targeted therapy in lung cancer. Proc Am Thorac Soc. 2012; 9: 72-73.
-
(2012)
Proc Am Thorac Soc
, vol.9
, pp. 72-73
-
-
Pao, W.1
-
21
-
-
0036726044
-
The US National Library of Medicine in the 21st century: Expanding collections, nontraditional formats, new audiences
-
Lacroix EM, Mehnert R,. The US National Library of Medicine in the 21st century: expanding collections, nontraditional formats, new audiences. Health Info Libr J. 2002; 19: 126-132.
-
(2002)
Health Info Libr J
, vol.19
, pp. 126-132
-
-
Lacroix, E.M.1
Mehnert, R.2
-
22
-
-
84890328625
-
SeqReporter: Automating next-generation sequencing result interpretation and reporting workflow in a clinical laboratory
-
Roy S, Durso MB, Wald A, et al., 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
Durso, M.B.2
Wald, A.3
|