-
1
-
-
77950633122
-
Integrative analysis of the melanoma transcriptome
-
Berger, M.F. et al. (2010) Integrative analysis of the melanoma transcriptome. Genome Res. 20, 413-427.
-
(2010)
Genome Res.
, vol.20
, pp. 413-427
-
-
Berger, M.F.1
-
2
-
-
84879890360
-
Comprehensive molecular characterization of clear cell renal cell carcinoma
-
Cancer Genome Atlas Research Network.
-
Cancer Genome Atlas Research Network. (2013) Comprehensive molecular characterization of clear cell renal cell carcinoma. Nature, 499, 43-49.
-
(2013)
Nature
, vol.499
, pp. 43-49
-
-
-
3
-
-
84861743958
-
RNA-SeQC: RNA-seq metrics for quality control and process optimization
-
DeLuca, D.S. et al. (2012) RNA-SeQC: RNA-seq metrics for quality control and process optimization. Bioinformatics, 28, 1530-1532.
-
(2012)
Bioinformatics
, vol.28
, pp. 1530-1532
-
-
DeLuca, D.S.1
-
4
-
-
39749197456
-
Genotype, haplotype and copy-number variation in worldwide human populations
-
Jakobsson, M. et al. (2008) Genotype, haplotype and copy-number variation in worldwide human populations. Nature, 451, 998-1003.
-
(2008)
Nature
, vol.451
, pp. 998-1003
-
-
Jakobsson, M.1
-
5
-
-
80051507403
-
TopHat-Fusion: An algorithm for discovery of novel fusion transcripts
-
Kim, D. and Salzberg, S.L. (2012) TopHat-Fusion: An algorithm for discovery of novel fusion transcripts. Genome Biol., 12, R72.
-
(2012)
Genome Biol.
, vol.12
-
-
Kim, D.1
Salzberg, S.L.2
-
6
-
-
67649884743
-
Fast and accurate short read alignment with burrows wheeler transform
-
Li, H. and Durbin, R. (2009) Fast and accurate short read alignment with burrows wheeler transform. Bioinformatics, 25, 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
7
-
-
68549104404
-
The sequence alignment/map format and SAMtools
-
Li, H. et al. (2009) The sequence alignment/map format and SAMtools. Bioinformatics, 25, 2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
-
8
-
-
77956295988
-
The genome analysis toolkit: AMapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna, A. et al. (2010) The genome analysis toolkit: AMapReduce framework for analyzing next-generation DNA sequencing data. Genome Res., 20, 1297-1303.
-
(2010)
Genome Res.
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
-
9
-
-
79957829805
-
DeFuse: An algorithm for gene fusion discovery in tumor RNA-Seq data
-
McPherson, A. et al. (2011) deFuse: An algorithm for gene fusion discovery in tumor RNA-Seq data. PLoS Comput. Biol., 7, e1001138.
-
(2011)
PLoS Comput. Biol.
, vol.7
-
-
McPherson, A.1
-
10
-
-
84865805666
-
Transforming fusions of FGFR and TACC genes in human glioblastoma
-
Singh, D. et al. (2012) Transforming fusions of FGFR and TACC genes in human glioblastoma. Science, 377, 1231-1235.
-
(2012)
Science
, vol.377
, pp. 1231-1235
-
-
Singh, D.1
-
11
-
-
73649123907
-
Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1
-
Verhaak, R.G.W. et al. (2010) Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. Cancer Cell, 17, 98-110.
-
(2010)
Cancer Cell
, vol.17
, pp. 98-110
-
-
Verhaak, R.G.W.1
-
12
-
-
84879764400
-
A survey of intragenic breakpoints in glioblastoma identifies a distinct subset associated with poor survival
-
Zheng, S. et al. (2013) A survey of intragenic breakpoints in glioblastoma identifies a distinct subset associated with poor survival. Genes Dev., 27, 1462-1472.
-
(2013)
Genes Dev.
, vol.27
, pp. 1462-1472
-
-
Zheng, S.1
|