-
1
-
-
79951970227
-
CNVnator: an approach to discover, genotype and characterize typical and atypical CNVs from family and population genome sequencing
-
Abyzov, A., Urban, A., Snyder, M. and Gerstein, M. (2011) CNVnator: an approach to discover, genotype and characterize typical and atypical CNVs from family and population genome sequencing. Genome Res., 21, 974-984.
-
(2011)
Genome Res.
, vol.21
, pp. 974-984
-
-
Abyzov, A.1
Urban, A.2
Snyder, M.3
Gerstein, M.4
-
2
-
-
79954672317
-
Genome structural variation discovery and genotyping
-
Alkan, C., Coe, B. and Eichler, E. (2011) Genome structural variation discovery and genotyping. Nat. Rev. Genet., 12, 363-375.
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 363-375
-
-
Alkan, C.1
Coe, B.2
Eichler, E.3
-
3
-
-
23744478860
-
Near-optimal detection of geometric objects by fast multiscale methods
-
Arias-Castro, E., Donoho, D. and Huo, X. (2005) Near-optimal detection of geometric objects by fast multiscale methods. IEEE Trans. Inform. Theor., 51, 2402-2425.
-
(2005)
IEEE Trans. Inform. Theor.
, vol.51
, pp. 2402-2425
-
-
Arias-Castro, E.1
Donoho, D.2
Huo, X.3
-
4
-
-
77956837921
-
Model-based quality assessment and base-calling for second-generation sequencing data
-
Bravo, H. and Irizarry, R. (2010) Model-based quality assessment and base-calling for second-generation sequencing data. Biometrics, 66, 665-674.
-
(2010)
Biometrics
, vol.66
, pp. 665-674
-
-
Bravo, H.1
Irizarry, R.2
-
5
-
-
54349125331
-
Robust nonparametric estimation via wavelet median regression
-
Brown, L. D., Cai, T. T. and Zhou, H. H. (2008) Robust nonparametric estimation via wavelet median regression. Ann. Statist., 36, 2055-2084.
-
(2008)
Ann. Statist.
, vol.36
, pp. 2055-2084
-
-
Brown, L.D.1
Cai, T.T.2
Zhou, H.H.3
-
6
-
-
80054739578
-
-
Optimal detection of heterogeneous and heteroscedastic mixtures. J. R. Statist. Soc. B
-
Cai, T. T., Jeng, X. J. and Jin, J. (2011) Optimal detection of heterogeneous and heteroscedastic mixtures. J. R. Statist. Soc. B, 73, 629-662.
-
(2011)
, vol.73
, pp. 629-662
-
-
Cai, T.T.1
Jeng, X.J.2
Jin, J.3
-
7
-
-
70049114041
-
Asymptotic equivalence and adaptive estimation for robust nonparametric regression
-
Cai, T. T. and Zhou, H. H. (2009) Asymptotic equivalence and adaptive estimation for robust nonparametric regression. Ann. Statist., 37, 3204-3235.
-
(2009)
Ann. Statist.
, vol.37
, pp. 3204-3235
-
-
Cai, T.T.1
Zhou, H.H.2
-
8
-
-
69549116107
-
BreakDancer: an algorithm for high-resolution mapping of genomic structural variation
-
Chen, K., Wallis, J., McLellan, M., Larson, D., Kalick, J., Pohl, C., McGrath, S., Wendl, M., Zhang, Q., Locke, D., Sho, X., Fulton, R., Ley, T., Ding, L. and Mardis, E. (2009) BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. Nat. Meth., 6, 677-681.
-
(2009)
Nat. Meth.
, vol.6
, pp. 677-681
-
-
Chen, K.1
Wallis, J.2
McLellan, M.3
Larson, D.4
Kalick, J.5
Pohl, C.6
McGrath, S.7
Wendl, M.8
Zhang, Q.9
Locke, D.10
Sho, X.11
Fulton, R.12
Ley, T.13
Ding, L.14
Mardis, E.15
-
9
-
-
80052990473
-
Systematic bias in high-throughput sequencing data and its correction by BEADS
-
to be published, doi:10.1093/nar/gkr425.
-
Cheung, M., Down, T., Latorre, I. and Ahringer, J. (2011) Systematic bias in high-throughput sequencing data and its correction by BEADS. Nucleic Acids Res., to be published, doi:10.1093/nar/gkr425.
-
(2011)
Nucleic Acids Res.
-
-
Cheung, M.1
Down, T.2
Latorre, I.3
Ahringer, J.4
-
10
-
-
58149218240
-
High-resolution mapping of copy-number alterations with massively parallel sequencing
-
Chiang, D., Getz, G., Jaffe, D., O'Kelly, M., Zhao, X., Carter, S., Russ, C., Nusbaum, C., Meyerson, M. and Lander, E. (2009) High-resolution mapping of copy-number alterations with massively parallel sequencing. Nat. Meth., 6, 99-103.
-
(2009)
Nat. Meth.
, vol.6
, pp. 99-103
-
-
Chiang, D.1
Getz, G.2
Jaffe, D.3
O'Kelly, M.4
Zhao, X.5
Carter, S.6
Russ, C.7
Nusbaum, C.8
Meyerson, M.9
Lander, E.10
-
11
-
-
67649289900
-
Copy number variation at 1q21.1 associated with neuroblastoma
-
Diskin, S. J., Hou, C., Glessner, J. T., Attiyeh, E. F., Laudenslager, M., Bosse, K., Cole, K., Moss, Y., Wood, A., Lynch, J. E., Pecor, K., Diamond, M., Winter, C., Wang, K., Kim, C., Geiger, E. A., McGrady, P. W., Blakemore, A. I. F., London, W. B., Shaikh, T. H., Bradfield, J., Grant, S. F. A., Li, H., Devoto, M., Rappaport, E. R., Hakonarson, H. and Maris, J. M. (2009) Copy number variation at 1q21.1 associated with neuroblastoma. Nature, 459, 987-991.
-
(2009)
Nature
, vol.459
, pp. 987-991
-
-
Diskin, S.J.1
Hou, C.2
Glessner, J.T.3
Attiyeh, E.F.4
Laudenslager, M.5
Bosse, K.6
Cole, K.7
Moss, Y.8
Wood, A.9
Lynch, J.E.10
Pecor, K.11
Diamond, M.12
Winter, C.13
Wang, K.14
Kim, C.15
Geiger, E.A.16
McGrady, P.W.17
Blakemore, A.I.F.18
London, W.B.19
Shaikh, T.H.20
Bradfield, J.21
Grant, S.F.A.22
Li, H.23
Devoto, M.24
Rappaport, E.R.25
Hakonarson, H.26
Maris, J.M.27
more..
-
12
-
-
31144469134
-
Structural variation in the human genome
-
Feuk, L., Carson, A. and Scherer, S. (2006) Structural variation in the human genome. Nat. Rev. Genet., 7, 85-97.
-
(2006)
Nat. Rev. Genet.
, vol.7
, pp. 85-97
-
-
Feuk, L.1
Carson, A.2
Scherer, S.3
-
13
-
-
79951748341
-
CNAseg-a novel framework for identification of copy number changes in cancer from second-generation sequencing data
-
Ivakhno, S., Royce, T., Cox, A., Evers, D., Cheetham, R. and Tavare, S. (2010) CNAseg-a novel framework for identification of copy number changes in cancer from second-generation sequencing data. Bioinformatics, 26, 3051-3058.
-
(2010)
Bioinformatics
, vol.26
, pp. 3051-3058
-
-
Ivakhno, S.1
Royce, T.2
Cox, A.3
Evers, D.4
Cheetham, R.5
Tavare, S.6
-
14
-
-
78649420973
-
Optimal sparse segment identification with application in copy number variation analysis
-
Jeng, J. J., Cai, T. T. and Li, H. (2010) Optimal sparse segment identification with application in copy number variation analysis. J. Am. Statist. Ass., 105, 1156-1166.
-
(2010)
J. Am. Statist. Ass.
, vol.105
, pp. 1156-1166
-
-
Jeng, J.J.1
Cai, T.T.2
Li, H.3
-
15
-
-
77955635446
-
rSW-seq: algorithm for detection of copy number alterations in deep sequencing data
-
article 432.
-
Kim, T., Luquette, L., Xi, R. and Park, J. (2010) rSW-seq: algorithm for detection of copy number alterations in deep sequencing data. BMC Bioinform., 11, article 432.
-
(2010)
BMC Bioinform.
, vol.11
-
-
Kim, T.1
Luquette, L.2
Xi, R.3
Park, J.4
-
16
-
-
77951940273
-
Modeling non-uniformity in short-read rates in RNA-Seq data
-
article
-
Li, J., Jiang, H. and Wong, W. (2010) Modeling non-uniformity in short-read rates in RNA-Seq data. Genome Biol., 11, article R50.
-
(2010)
Genome Biol.
, vol.11
-
-
Li, J.1
Jiang, H.2
Wong, W.3
-
17
-
-
79961181124
-
Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly
-
Li, Y., Zheng, H., Lou, R., Wu, H., Zhu, H., Li, R., Cao, H., Wu, B., Huang, S., Shao, H., Ma, H., Zhang, F., Feng, S., Zhang, W., Du, H., Tian, G., Li, J., Zhang, X., Li, S., Bolund, L., Kristiansen, K., de Smith, A., Blakemore, A., Coin, L., Yang, H. and Wang, J. (2011) Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly. Nat. Biotech., 29, 723-730.
-
(2011)
Nat. Biotech.
, vol.29
, pp. 723-730
-
-
Li, Y.1
Zheng, H.2
Lou, R.3
Wu, H.4
Zhu, H.5
Li, R.6
Cao, H.7
Wu, B.8
Huang, S.9
Shao, H.10
Ma, H.11
Zhang, F.12
Feng, S.13
Zhang, W.14
Du, H.15
Tian, G.16
Li, J.17
Zhang, X.18
Li, S.19
Bolund, L.20
Kristiansen, K.21
de Smith, A.22
Blakemore, A.23
Coin, L.24
Yang, H.25
Wang, J.26
more..
-
18
-
-
34347353237
-
Copy-number variation and association studies of human disease
-
McCarroll, S. S. and Altshuler, D. M. (2007) Copy-number variation and association studies of human disease. Nat. Genet., 39, suppl., S37-S42.
-
(2007)
Nat. Genet.
, vol.39
, Issue.SUPPL.
-
-
McCarroll, S.S.1
Altshuler, D.M.2
-
19
-
-
70449704529
-
Computational methods for discovering structural variation with next-generation sequencing
-
Medvedev, P., Stanciu, M. and Brudno, M. (2009) Computational methods for discovering structural variation with next-generation sequencing. Nat. Meth., 6, S13-S20.
-
(2009)
Nat. Meth.
, vol.6
-
-
Medvedev, P.1
Stanciu, M.2
Brudno, M.3
-
20
-
-
79551621409
-
ReadDepth: a parallel R package for detecting copy number alterations from short sequencing reads
-
article e16327.
-
Miller, C. A., Hampton, O., Coarfa, C. and Milosavljevic, A. (2011) ReadDepth: a parallel R package for detecting copy number alterations from short sequencing reads. PLOS ONE, 6, article e16327.
-
(2011)
PLOS ONE
, vol.6
-
-
Miller, C.A.1
Hampton, O.2
Coarfa, C.3
Milosavljevic, A.4
-
21
-
-
84975804424
-
Mapping copy number variation by population-scale genome sequencing
-
Mills, R. E., Walter, K., Stewart, C., Handsaker, R. E., Chen, K., Alkan, C., Abyzov, A., Yoon, S. C., Ye, K., Cheetham, R. K., Chinwalla, A., Conrad, D. F., Fu, Y., Grubert, F., Hajirasouliha, I., Hormozdiari, F., Iakoucheva, L. M., Iqbal, Z., Kang, S., Kidd, J. M., Konkel, M. K., Korn, J., Khurana, E., Kural, D., Lam, H. Y. K., Leng, J., Li, R., Li, Y., Lin, C.-Y., Luo, R., Mu, X. J., Nemesh, J., Peckham, H. E., Rausch, T., Scally, A., Shi, X., Stromberg, M. P., Sitz, A. M., Urban, A. E., Walker, J. A., Wu, J., Zhang, Y., Zhang, Z. D., Batzer, M. A., Ding, L., Marth, G. T., McVean, G., Sebat, J., Snyder, M., Wang, J., Ye, K., Eichler, E. E., Gerstein, M. B., Hurles, M. E., Lee, C., McCarroll, S. A. and Korbel, J. O. (2011) Mapping copy number variation by population-scale genome sequencing. Nature, 470, 59-65.
-
(2011)
Nature
, vol.470
, pp. 59-65
-
-
Mills, R.E.1
Walter, K.2
Stewart, C.3
Handsaker, R.E.4
Chen, K.5
Alkan, C.6
Abyzov, A.7
Yoon, S.C.8
Ye, K.9
Cheetham, R.K.10
Chinwalla, A.11
Conrad, D.F.12
Fu, Y.13
Grubert, F.14
Hajirasouliha, I.15
Hormozdiari, F.16
Iakoucheva, L.M.17
Iqbal, Z.18
Kang, S.19
Kidd, J.M.20
Konkel, M.K.21
Korn, J.22
Khurana, E.23
Kural, D.24
Lam, H.25
Leng, J.26
Li, R.27
Li, Y.28
Lin, C.-Y.29
Luo, R.30
Mu, X.J.31
Nemesh, J.32
Peckham, H.E.33
Rausch, T.34
Scally, A.35
Shi, X.36
Stromberg, M.P.37
Sitz, A.M.38
Urban, A.E.39
Walker, J.A.40
Wu, J.41
Zhang, Y.42
Zhang, Z.D.43
Batzer, M.A.44
Ding, L.45
Marth, G.T.46
McVean, G.47
Sebat, J.48
Snyder, M.49
Wang, J.50
Ye, K.51
Eichler, E.E.52
Gerstein, M.B.53
Hurles, M.E.54
Lee, C.55
McCarroll, S.A.56
Korbel, J.O.57
more..
-
22
-
-
79953855362
-
Accurate and exact CNV identification from targeted high-throughput sequence data
-
article 184.
-
Nord, A., Lee, M., King, M. and Walsh, T. (2011) Accurate and exact CNV identification from targeted high-throughput sequence data. BMC Genom., 12, article 184.
-
(2011)
BMC Genom.
, vol.12
-
-
Nord, A.1
Lee, M.2
King, M.3
Walsh, T.4
-
23
-
-
3543105225
-
Circular binary segmentation for the analysis of array-based DNA copy number data
-
Olshen, A. B., Venkatraman, E. S., Lucito, R. and Wigler, M. (2004) Circular binary segmentation for the analysis of array-based DNA copy number data. Biostatistics, 5, 557-572.
-
(2004)
Biostatistics
, vol.5
, pp. 557-572
-
-
Olshen, A.B.1
Venkatraman, E.S.2
Lucito, R.3
Wigler, M.4
-
24
-
-
0036898577
-
Microarray data normalization and transformation
-
Quackenbush, J. (2002) Microarray data normalization and transformation. Nat. Genet., 32, 496-501.
-
(2002)
Nat. Genet.
, vol.32
, pp. 496-501
-
-
Quackenbush, J.1
-
25
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon, R., Ishikawa, S., Fitch, K., Feuk, L., Perry, G., Andrews, T., Fiegler, H., Shapero, M., Carson, A., Chen, W., Cho, E., Dallaire, S., Freeman, J., Gonzalez, J., Gratacs, M., Huang, J., Kalaitzopoulos, D., Komura, D., MacDonald, J., Marshall, C., Mei, R., Montgomery, L., Nishimura, K., Okamura, K., Shen, F., Somerville, M., Tchinda, J., Valsesia, A., Woodwark, C., Yang, F., Zhang, J., Zerjal, T., Zhang, J., Armengol, L., Conrad, D., Estivill, X., Tyler-Smith, C., Carter, N., Aburatani, H., Lee, C., Jones, K., Scherer, S. and Hurles, M. (2006) Global variation in copy number in the human genome. Nature, 444, 444-454.
-
(2006)
Nature
, vol.444
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.3
Feuk, L.4
Perry, G.5
Andrews, T.6
Fiegler, H.7
Shapero, M.8
Carson, A.9
Chen, W.10
Cho, E.11
Dallaire, S.12
Freeman, J.13
Gonzalez, J.14
Gratacs, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.19
Marshall, C.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Zhang, J.33
Armengol, L.34
Conrad, D.35
Estivill, X.36
Tyler-Smith, C.37
Carter, N.38
Aburatani, H.39
Lee, C.40
Jones, K.41
Scherer, S.42
Hurles, M.43
more..
-
26
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat, J., Lakshmi, B., Troge, J., Alexander, J., Young, J., Lundin, P., Maner, S., Massa, H., Walker, M., Chi, M., Navin, N., Lucito, R., Healy, J., Hicks, J., Ye, K., Reiner, A., Gilliam, T., Trask, B., Patterson, N., Zetterberg, A. and Wigler, M.(2004) Large-scale copy number polymorphism in the human genome. Science, 305, 525-528.
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
Lundin, P.6
Maner, S.7
Massa, H.8
Walker, M.9
Chi, M.10
Navin, N.11
Lucito, R.12
Healy, J.13
Hicks, J.14
Ye, K.15
Reiner, A.16
Gilliam, T.17
Trask, B.18
Patterson, N.19
Zetterberg, A.20
Wigler, M.21
more..
-
27
-
-
53649106195
-
Next-generation DNA sequencing
-
Shendure, J. and Ji, H. (2008) Next-generation DNA sequencing. Nat. Biotech., 26, 1135-1145.
-
(2008)
Nat. Biotech.
, vol.26
, pp. 1135-1145
-
-
Shendure, J.1
Ji, H.2
-
28
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson, H., Rujescu, D., Cichon, S., Pietilainen, O., Ingason, A., Steinberg, A., Fossdal, R., Sigurdsson, E., Sigmundsson, T., Buizer-Voskamp, J. et al. (2008) Large recurrent microdeletions associated with schizophrenia. Nature, 455, 178-179.
-
(2008)
Nature
, vol.455
, pp. 178-179
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietilainen, O.4
Ingason, A.5
Steinberg, A.6
Fossdal, R.7
Sigurdsson, E.8
Sigmundsson, T.9
Buizer-Voskamp, J.10
-
29
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
Stone, J., O'Donovan, M., Gurling, H., Kirov, G., Blackwood, D., Corvin, A., Craddock, N., Gill, M., Hultman, C., Lichtenstein, P. et al. (2008) Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature, 455, 237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
Stone, J.1
O'Donovan, M.2
Gurling, H.3
Kirov, G.4
Blackwood, D.5
Corvin, A.6
Craddock, N.7
Gill, M.8
Hultman, C.9
Lichtenstein, P.10
-
30
-
-
33645243394
-
High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays
-
Urban, A., Korbel, J., Selzer, R., Richmond, T., Hacker, A., Popescu, G., Cubells, J., Green, R., Emanuel, B., Gerstein, M., Weissman, S. and Snyder, M. (2006) High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays. Proc. Natn. Acad. Sci. USA, 103, 4534-4539.
-
(2006)
Proc. Natn. Acad. Sci. USA
, vol.103
, pp. 4534-4539
-
-
Urban, A.1
Korbel, J.2
Selzer, R.3
Richmond, T.4
Hacker, A.5
Popescu, G.6
Cubells, J.7
Green, R.8
Emanuel, B.9
Gerstein, M.10
Weissman, S.11
Snyder, M.12
-
31
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
Walsh, T., McClellan, J. M., McCarthy, S. E., Addington, A. M., Pierce, S. B., Cooper, G. M., Nord, A. S., Kusenda, M., Malhotra, D., Bhandari, A., Stray, S. M., Rippey, C. F., Roccanova, P., Makarov, V., Lakshmi, B., Findley, R. L., Sikich, L., Stromberg, T., Merriman, B., Gogtay, N., Butler, P., Eckstrand, K., Noory, L., Gochman, P., Long, R., Chen, Z., Davis, S., Baker, C., Eichler, E. E., Meltzer, P. S., Nelson, S. F., Singleton, A. B., Lee, M. K., Rapoport, J. L., King, M.-C. and Sebat, J. (2008) Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science, 320, 539-543.
-
(2008)
Science
, vol.320
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
Addington, A.M.4
Pierce, S.B.5
Cooper, G.M.6
Nord, A.S.7
Kusenda, M.8
Malhotra, D.9
Bhandari, A.10
Stray, S.M.11
Rippey, C.F.12
Roccanova, P.13
Makarov, V.14
Lakshmi, B.15
Findley, R.L.16
Sikich, L.17
Stromberg, T.18
Merriman, B.19
Gogtay, N.20
Butler, P.21
Eckstrand, K.22
Noory, L.23
Gochman, P.24
Long, R.25
Chen, Z.26
Davis, S.27
Baker, C.28
Eichler, E.E.29
Meltzer, P.S.30
Nelson, S.F.31
Singleton, A.B.32
Lee, M.K.33
Rapoport, J.L.34
King, M.-C.35
Sebat, J.36
more..
-
32
-
-
77649323880
-
Optimal and fast detection of spacial clusters with scan statistics
-
Walther, G. (2010) Optimal and fast detection of spacial clusters with scan statistics. Ann. Statist., 38, 1010-1033.
-
(2010)
Ann. Statist.
, vol.38
, pp. 1010-1033
-
-
Walther, G.1
-
33
-
-
64849083125
-
CNV-seq, a new method to detect copy number variation using high-throughput sequencing
-
article.
-
Xie, C. and Tammi, M. (2009) CNV-seq, a new method to detect copy number variation using high-throughput sequencing. BMC Bioinform., 10, article80.
-
(2009)
BMC Bioinform.
, vol.10
, pp. 80
-
-
Xie, C.1
Tammi, M.2
-
34
-
-
69749122557
-
Sensitive and accurate detection of copy number variants using read depth of coverage
-
Yoon, S., Xuan, Z., Makarov, V., Ye, K. and Sebat, J. (2009) Sensitive and accurate detection of copy number variants using read depth of coverage. Genome Res., 19, 1568-1592.
-
(2009)
Genome Res.
, vol.19
, pp. 1568-1592
-
-
Yoon, S.1
Xuan, Z.2
Makarov, V.3
Ye, K.4
Sebat, J.5
-
35
-
-
70350221909
-
Copy number variation in human health, disease and evolutions
-
Zhang, F., Gu, W., Hurles, M. and Lupski, J. (2009) Copy number variation in human health, disease and evolutions. A. Rev. Genom. Hum. Genet., 10, 451-481.
-
(2009)
A. Rev. Genom. Hum. Genet.
, vol.10
, pp. 451-481
-
-
Zhang, F.1
Gu, W.2
Hurles, M.3
Lupski, J.4
-
36
-
-
84867628055
-
A note on quantile coupling inequalities and their applications.
-
Department of Statistics, Yale University, New Haven.
-
Zhou, H. (2006) A note on quantile coupling inequalities and their applications.. Technical Report. Department of Statistics, Yale University, New Haven.
-
(2006)
Technical Report
-
-
Zhou, H.1
|