-
1
-
-
84885865195
-
The value of statistical or bioinformatics annotation for rare variant association with quantitative trait
-
Byrnes, A.E. et al. (2013) The value of statistical or bioinformatics annotation for rare variant association with quantitative trait. Genet. Epidemiol., 37, 666-674.
-
(2013)
Genet. Epidemiol.
, vol.37
, pp. 666-674
-
-
Byrnes, A.E.1
-
3
-
-
84911435067
-
RAREMETAL: Fast and powerful meta-Analysis for rare variants
-
Feng, S. et al. (2014) RAREMETAL: fast and powerful meta-Analysis for rare variants. Bioinformatics, 30, 2828-2829.
-
(2014)
Bioinformatics
, vol.30
, pp. 2828-2829
-
-
Feng, S.1
-
4
-
-
0002178053
-
Bias reduction of maximum likelihood estimates
-
Firth, D. (1993) Bias reduction of maximum likelihood estimates. Biometrika, 80, 27-38.
-
(1993)
Biometrika
, vol.80
, pp. 27-38
-
-
Firth, D.1
-
5
-
-
84904025285
-
A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data
-
Hu, H. et al. (2014) A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. Nat. Biotechnol., 32, 663-669.
-
(2014)
Nat. Biotechnol.
, vol.32
, pp. 663-669
-
-
Hu, H.1
-
6
-
-
62649084535
-
Power of deep, all-exon resequencing for discovery of human trait genes
-
Kryukov, G.V. et al. (2009) Power of deep, all-exon resequencing for discovery of human trait genes. Proc Natl Acad Sci USA, 106, 3871-3876.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 3871-3876
-
-
Kryukov, G.V.1
-
7
-
-
84904006087
-
Rare-variant association analysis: Study designs and statistical tests
-
Lee, S. et al. (2014) Rare-variant association analysis: study designs and statistical tests. Am. J. Hum. Genet., 95, 5-23.
-
(2014)
Am. J. Hum. Genet.
, vol.95
, pp. 5-23
-
-
Lee, S.1
-
8
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data
-
Li, B. and Leal, S.M. (2008) Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am. J. Hum. Genet., 83, 311-321.
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 311-321
-
-
Li, B.1
Leal, S.M.2
-
9
-
-
80053372166
-
FaST linear mixed models for genome-wide association studies
-
Lippert, C. et al. (2011) FaST linear mixed models for genome-wide association studies. Nat. Methods, 8, 833-835.
-
(2011)
Nat. Methods
, vol.8
, pp. 833-835
-
-
Lippert, C.1
-
10
-
-
84877772904
-
FaST-LMM-Select for addressing confounding from spatial structure and rare variants
-
Listgarten, J. et al. (2013) FaST-LMM-Select for addressing confounding from spatial structure and rare variants. Nat. Genet., 45, 470-471.
-
(2013)
Nat. Genet.
, vol.45
, pp. 470-471
-
-
Listgarten, J.1
-
11
-
-
84895808047
-
Meta-Analysis of gene-level tests for rare variant association
-
Liu, D.J. et al. (2014) Meta-Analysis of gene-level tests for rare variant association. Nat. Genet., 46, 200-204.
-
(2014)
Nat. Genet.
, vol.46
, pp. 200-204
-
-
Liu, D.J.1
-
12
-
-
84881614989
-
Recommended joint and meta-Analysis strategies for casecontrol association testing of single low-count variants
-
Ma, C. et al. (2013) Recommended joint and meta-Analysis strategies for casecontrol association testing of single low-count variants. Genet. Epidemiol., 37, 539-550.
-
(2013)
Genet. Epidemiol.
, vol.37
, pp. 539-550
-
-
Ma, C.1
-
13
-
-
84898723939
-
Joint analysis of functional genomic data and genome-wide association studies of 18 human traits
-
Pickrell, J.K. (2014) Joint analysis of functional genomic data and genome-wide association studies of 18 human traits.Am. J. Hum. Genet., 94, 559-573.
-
(2014)
Am J. Hum. Genet.
, vol.94
, pp. 559-573
-
-
Pickrell, J.K.1
-
14
-
-
84899859455
-
Variant association tools for quality control and analysis of large-scale sequence and genotyping array data
-
Wang, G.T. et al. (2014) Variant association tools for quality control and analysis of large-scale sequence and genotyping array data. Am. J. Hum. Genet., 94, 770-783.
-
(2014)
Am. J. Hum. Genet.
, vol.94
, pp. 770-783
-
-
Wang, G.T.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
, pp. e164
-
-
Wang, K.1
-
16
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu, M.C. et al. (2011) Rare-variant association testing for sequencing data with the sequence kernel association test. Am. J. Hum. Genet., 89, 82-93.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
-
17
-
-
80051547469
-
A probabilistic disease-gene finder for personal genomes
-
Yandell, M. et al. (2011) A probabilistic disease-gene finder for personal genomes. Genome Res., 21, 1529-1542.
-
(2011)
Genome Res.
, vol.21
, pp. 1529-1542
-
-
Yandell, M.1
-
18
-
-
84954389230
-
Seqminer: An R-package to facilitate the functional interpretation of sequence-based associations
-
Zhan, X. and Liu, D.J. (2015) SEQMINER: an R-package to facilitate the functional interpretation of sequence-based associations. Genet. Epidemiol., 39, 619-623.
-
(2015)
Genet. Epidemiol.
, vol.39
, pp. 619-623
-
-
Zhan, X.1
Liu, D.J.2
|