-
1
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis, G.R. et al. (2002) Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat. Genet., 30, 97-101.
-
(2002)
Nat. Genet.
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
-
2
-
-
79960405019
-
The variant call format and VCFtools
-
Danecek, P. et al. (2011) The variant call format and VCFtools. Bioinformatics, 27, 2156-2158.
-
(2011)
Bioinformatics
, vol.27
, pp. 2156-2158
-
-
Danecek, P.1
-
3
-
-
77950301214
-
Variance component model to account for sample structure in genome-wide association studies
-
Kang, H.M. et al. (2010) Variance component model to account for sample structure in genome-wide association studies. Nat. Genet., 42, 348-354.
-
(2010)
Nat. Genet.
, vol.42
, pp. 348-354
-
-
Kang, H.M.1
-
4
-
-
84880294630
-
General framework for meta-analysis of rare variants in sequencing association studies
-
Lee, S. et al. (2013) General framework for meta-analysis of rare variants in sequencing association studies. Am. J. Hum. Genet., 93, 42-53.
-
(2013)
Am. J. Hum. Genet.
, vol.93
, pp. 42-53
-
-
Lee, S.1
-
5
-
-
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
-
6
-
-
80052731371
-
A general framework for detecting disease associations with rare variants in sequencing studies
-
Lin, D.Y. and Tang, Z.Z. (2011) A general framework for detecting disease associations with rare variants in sequencing studies. Am. J. Hum. Genet., 89, 354-367.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 354-367
-
-
Lin, D.Y.1
Tang, Z.Z.2
-
7
-
-
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
-
8
-
-
84895808047
-
Meta-analysis of gene-level tests for rare variant association
-
Liu, D. 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.1
-
10
-
-
61449168010
-
A groupwise association test for rare mutations using a weighted sum statistic
-
Madsen, B.E. and Browning, S.R. (2009) A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet., 5, e1000384.
-
(2009)
PLoS Genet.
, vol.5
, pp. e1000384
-
-
Madsen, B.E.1
Browning, S.R.2
-
11
-
-
77953121877
-
Pooled association tests for rare variants in exon-resequen-cing studies
-
Price, A.L. et al. (2010) Pooled association tests for rare variants in exon-resequen-cing studies. Am. J. Hum. Genet., 86, 832-838.
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 832-838
-
-
Price, A.L.1
-
12
-
-
84880198559
-
MASS: Meta-analysis of score statistics for sequencing studies
-
Tang, Z.Z. and Lin, D.Y. (2013) MASS: meta-analysis of score statistics for sequencing studies. Bioinformatics, 29, 1803-1805.
-
(2013)
Bioinformatics
, vol.29
, pp. 1803-1805
-
-
Tang, Z.Z.1
Lin, D.Y.2
-
14
-
-
77955894071
-
METAL: Fast and efficient meta-analysis of genomewide association scans
-
Willer, C.J. et al. (2010) METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics, 26, 2190-2191.
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
-
15
-
-
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
|