-
1
-
-
84878799611
-
Predicting functional effect of human missense mutations using PolyPhen-2
-
Chapter 7, Unit 7.20
-
Adzhubei, I. et al. (2013) Predicting functional effect of human missense mutations using PolyPhen-2. Curr Protoc Hum Genet., Chapter 7, Unit 7.20.
-
(2013)
Curr Protoc Hum Genet.
-
-
Adzhubei, I.1
-
2
-
-
84864294140
-
WANNOVAR: Annotating genetic variants for personal genomes via the web
-
Chang, X. and Wang, K. (2012) wANNOVAR: annotating genetic variants for personal genomes via the web. J. Med. Genet., 49, 433-436.
-
(2012)
J. Med. Genet.
, vol.49
, pp. 433-436
-
-
Chang, X.1
Wang, K.2
-
3
-
-
84874732372
-
CRAVAT: Cancer-related analysis of variants toolkit
-
Douville, C. et al. (2013) CRAVAT: cancer-related analysis of variants toolkit. Bioinformatics, 29, 647-648.
-
(2013)
Bioinformatics
, vol.29
, pp. 647-648
-
-
Douville, C.1
-
4
-
-
57549098807
-
The catalogue of somatic mutations in cancer (COSMIC)
-
Chapter 10, Unit 10 11
-
Forbes, S.A. et al. (2008) The Catalogue of Somatic Mutations in Cancer (COSMIC). Curr. Protoc. Hum. Genet., Chapter 10, Unit 10 11.
-
(2008)
Curr. Protoc. Hum. Genet.
-
-
Forbes, S.A.1
-
5
-
-
84886247811
-
Assessment of computational methods for predicting the effects of missense mutations in human cancers
-
Gnad, F. et al. (2013) Assessment of computational methods for predicting the effects of missense mutations in human cancers. BMC Genomics, 14 (Suppl. 3), S7.
-
(2013)
BMC Genomics
, vol.14
, Issue.SUPPL. 3
-
-
Gnad, F.1
-
6
-
-
84858983547
-
KEGG for integration and interpretation of large-scale molecular data sets
-
Kanehisa, M. et al. (2012) KEGG for integration and interpretation of large-scale molecular data sets. Nucleic Acids Res., 40, D109-D114.
-
(2012)
Nucleic Acids Res.
, vol.40
-
-
Kanehisa, M.1
-
7
-
-
84858384405
-
Interpretome: A freely available, modular, and secure personal genome interpretation engine
-
Karczewski, K.J. et al. (2012) Interpretome: a freely available, modular, and secure personal genome interpretation engine. Pac. Symp. Biocomput., 2012, 339-350.
-
(2012)
Pac. Symp. Biocomput.
, vol.2012
, pp. 339-350
-
-
Karczewski, K.J.1
-
8
-
-
84859740873
-
RNA-Seq Atlas-A reference database for gene expression profiling in normal tissue by next-generation sequencing
-
Krupp, M. et al. (2012) RNA-Seq Atlas-a reference database for gene expression profiling in normal tissue by next-generation sequencing. Bioinformatics, 28, 1184-1185.
-
(2012)
Bioinformatics
, vol.28
, pp. 1184-1185
-
-
Krupp, M.1
-
9
-
-
69649109364
-
Circos: An information aesthetic for comparative genomics
-
Krzywinski, M. et al. (2009) Circos: an information aesthetic for comparative genomics. Genome Res., 19, 1639-1645.
-
(2009)
Genome Res.
, vol.19
, pp. 1639-1645
-
-
Krzywinski, M.1
-
10
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
Kumar, P. et al. (2009) Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat. Protoc., 4, 1073-1081.
-
(2009)
Nat. Protoc.
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
-
11
-
-
84881613239
-
DbNSFP v2.0: A database of human non-synonymous SNVs and their functional predictions and annotations
-
Liu, X. et al. (2013) dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations. Hum. Mutat., 34, E2393-2402.
-
(2013)
Hum. Mutat.
, vol.34
-
-
Liu, X.1
-
12
-
-
84864486576
-
VARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing
-
Medina, I. et al. (2012) VARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing. Nucleic Acids Res., 40, W54-W58.
-
(2012)
Nucleic Acids Res.
, vol.40
-
-
Medina, I.1
-
13
-
-
84881085966
-
A survey of tools for variant analysis of next-generation genome sequencing data
-
[Epub ahead of print, January 21, 2013]
-
Pabinger, S. et al. (2013) A survey of tools for variant analysis of next-generation genome sequencing data. Brief. Bioinform., [Epub ahead of print, January 21, 2013].
-
(2013)
Brief. Bioinform.
-
-
Pabinger, S.1
-
14
-
-
77950644139
-
PhosSNP for systematic analysis of genetic polymorphisms that influence protein phosphorylation
-
Ren, J. et al. (2010) PhosSNP for systematic analysis of genetic polymorphisms that influence protein phosphorylation. Mol. Cell Proteomics, 9, 623-634.
-
(2010)
Mol. Cell Proteomics
, vol.9
, pp. 623-634
-
-
Ren, J.1
-
15
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
-
Wang, K. et al. (2010) ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res., 38, e164.
-
(2010)
Nucleic Acids Res.
, vol.38
-
-
Wang, K.1
|