-
1
-
-
33751329250
-
Global variation in copy number in the human genome
-
10.1038/nature05329, 2669898, 17122850
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W. Global variation in copy number in the human genome. Nature 2006, 444(7118):444-454. 10.1038/nature05329, 2669898, 17122850.
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
-
2
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
10.1038/ng1416, 15286789
-
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y, Scherer SW, Lee C. Detection of large-scale variation in the human genome. Nat Genet 2004, 36(9):949-951. 10.1038/ng1416, 15286789.
-
(2004)
Nat Genet
, vol.36
, Issue.9
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
Scherer, S.W.7
Lee, C.8
-
3
-
-
84975804424
-
Mapping copy number variation by population-scale genome sequencing
-
10.1038/nature09708, 3077050, 21293372
-
Mills RE, Walter K, Stewart C, Handsaker RE, Chen K, Alkan C, Abyzov A, Yoon SC, Ye K, Cheetham RK. Mapping copy number variation by population-scale genome sequencing. Nature 2011, 470(7332):59-65. 10.1038/nature09708, 3077050, 21293372.
-
(2011)
Nature
, vol.470
, Issue.7332
, 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
-
4
-
-
81055149805
-
Whole genome resequencing of black Angus and Holstein cattle for SNP and CNV discovery
-
10.1186/1471-2164-12-559, 3229636, 22085807
-
Stothard P, Choi JW, Basu U, Sumner-Thomson JM, Meng Y, Liao X, Moore SS. Whole genome resequencing of black Angus and Holstein cattle for SNP and CNV discovery. BMC Genomics 2011, 12:559. 10.1186/1471-2164-12-559, 3229636, 22085807.
-
(2011)
BMC Genomics
, vol.12
, pp. 559
-
-
Stothard, P.1
Choi, J.W.2
Basu, U.3
Sumner-Thomson, J.M.4
Meng, Y.5
Liao, X.6
Moore, S.S.7
-
5
-
-
81055149804
-
Global assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping
-
10.1186/1471-2164-12-557, 3248099, 22082336
-
Zhan B, Fadista J, Thomsen B, Hedegaard J, Panitz F, Bendixen C. Global assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping. BMC Genomics 2011, 12:557. 10.1186/1471-2164-12-557, 3248099, 22082336.
-
(2011)
BMC Genomics
, vol.12
, pp. 557
-
-
Zhan, B.1
Fadista, J.2
Thomsen, B.3
Hedegaard, J.4
Panitz, F.5
Bendixen, C.6
-
6
-
-
79952112002
-
Copy number variation in the porcine genome inferred from a 60 k SNP BeadChip
-
10.1186/1471-2164-11-593, 3091738, 20969757
-
Ramayo-Caldas Y, Castello A, Pena RN, Alves E, Mercade A, Souza CA, Fernandez AI, Perez-Enciso M, Folch JM. Copy number variation in the porcine genome inferred from a 60 k SNP BeadChip. BMC Genomics 2010, 11:593. 10.1186/1471-2164-11-593, 3091738, 20969757.
-
(2010)
BMC Genomics
, vol.11
, pp. 593
-
-
Ramayo-Caldas, Y.1
Castello, A.2
Pena, R.N.3
Alves, E.4
Mercade, A.5
Souza, C.A.6
Fernandez, A.I.7
Perez-Enciso, M.8
Folch, J.M.9
-
7
-
-
84865865592
-
Copy number variation in the genomes of domestic animals
-
Clop A, Vidal O, Amills M. Copy number variation in the genomes of domestic animals. Anim Genet 2011, 43.
-
(2011)
Anim Genet
, vol.43
-
-
Clop, A.1
Vidal, O.2
Amills, M.3
-
8
-
-
84859535421
-
Copy number variation of individual cattle genomes using next-generation sequencing
-
10.1101/gr.133967.111, 3317159, 22300768
-
Bickhart DM, Hou Y, Schroeder SG, Alkan C, Cardone MF, Matukumalli LK, Song J, Schnabel RD, Ventura M, Taylor JF. Copy number variation of individual cattle genomes using next-generation sequencing. Genome Res 2012, 22(4):778-790. 10.1101/gr.133967.111, 3317159, 22300768.
-
(2012)
Genome Res
, vol.22
, Issue.4
, pp. 778-790
-
-
Bickhart, D.M.1
Hou, Y.2
Schroeder, S.G.3
Alkan, C.4
Cardone, M.F.5
Matukumalli, L.K.6
Song, J.7
Schnabel, R.D.8
Ventura, M.9
Taylor, J.F.10
-
9
-
-
61849154119
-
Mapping DNA structural variation in dogs
-
2661804, 19015322
-
Chen WK, Swartz JD, Rush LJ, Alvarez CE. Mapping DNA structural variation in dogs. Genome Res 2009, 19(3):500-509. 2661804, 19015322.
-
(2009)
Genome Res
, vol.19
, Issue.3
, pp. 500-509
-
-
Chen, W.K.1
Swartz, J.D.2
Rush, L.J.3
Alvarez, C.E.4
-
10
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
-
10.1038/35057149, 11237013
-
Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, Mullikin JC, Mortimore BJ, Willey DL. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 2001, 409(6822):928-933. 10.1038/35057149, 11237013.
-
(2001)
Nature
, vol.409
, Issue.6822
, pp. 928-933
-
-
Sachidanandam, R.1
Weissman, D.2
Schmidt, S.C.3
Kakol, J.M.4
Stein, L.D.5
Marth, G.6
Sherry, S.7
Mullikin, J.C.8
Mortimore, B.J.9
Willey, D.L.10
-
11
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
10.1126/science.1098918, 15273396
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, Maner S, Massa H, Walker M, Chi M. Large-scale copy number polymorphism in the human genome. Science 2004, 305(5683):525-528. 10.1126/science.1098918, 15273396.
-
(2004)
Science
, vol.305
, Issue.5683
, 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
-
12
-
-
31144469134
-
Structural variation in the human genome
-
Feuk L, Carson AR, Scherer SW. Structural variation in the human genome. Nat Rev Genet 2006, 7(2):85-97.
-
(2006)
Nat Rev Genet
, vol.7
, Issue.2
, pp. 85-97
-
-
Feuk, L.1
Carson, A.R.2
Scherer, S.W.3
-
13
-
-
79954672317
-
Genome structural variation discovery and genotyping
-
10.1038/nrg2958, 21358748
-
Alkan C, Coe BP, Eichler EE. Genome structural variation discovery and genotyping. Nat Rev Genet 2011, 12(5):363-376. 10.1038/nrg2958, 21358748.
-
(2011)
Nat Rev Genet
, vol.12
, Issue.5
, pp. 363-376
-
-
Alkan, C.1
Coe, B.P.2
Eichler, E.E.3
-
14
-
-
77951719393
-
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
-
10.1038/ng.555, 3329635, 20364138
-
Park H, Kim JI, Ju YS, Gokcumen O, Mills RE, Kim S, Lee S, Suh D, Hong D, Kang HP. Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing. Nat Genet 2010, 42(5):400-405. 10.1038/ng.555, 3329635, 20364138.
-
(2010)
Nat Genet
, vol.42
, Issue.5
, pp. 400-405
-
-
Park, H.1
Kim, J.I.2
Ju, Y.S.3
Gokcumen, O.4
Mills, R.E.5
Kim, S.6
Lee, S.7
Suh, D.8
Hong, D.9
Kang, H.P.10
-
15
-
-
77952296952
-
Towards a comprehensive structural variation map of an individual human genome
-
10.1186/gb-2010-11-5-r52, 2898065, 20482838
-
Pang AW, MacDonald JR, Pinto D, Wei J, Rafiq MA, Conrad DF, Park H, Hurles ME, Lee C, Venter JC. Towards a comprehensive structural variation map of an individual human genome. Genome Biol 2010, 11(5):R52. 10.1186/gb-2010-11-5-r52, 2898065, 20482838.
-
(2010)
Genome Biol
, vol.11
, Issue.5
-
-
Pang, A.W.1
MacDonald, J.R.2
Pinto, D.3
Wei, J.4
Rafiq, M.A.5
Conrad, D.F.6
Park, H.7
Hurles, M.E.8
Lee, C.9
Venter, J.C.10
-
16
-
-
78049412267
-
Diversity of human copy number variation and multicopy genes
-
10.1126/science.1197005, 3020103, 21030649
-
Sudmant PH, Kitzman JO, Antonacci F, Alkan C, Malig M, Tsalenko A, Sampas N, Bruhn L, Shendure J, Eichler EE. Diversity of human copy number variation and multicopy genes. Science 2010, 330(6004):641-646. 10.1126/science.1197005, 3020103, 21030649.
-
(2010)
Science
, vol.330
, Issue.6004
, pp. 641-646
-
-
Sudmant, P.H.1
Kitzman, J.O.2
Antonacci, F.3
Alkan, C.4
Malig, M.5
Tsalenko, A.6
Sampas, N.7
Bruhn, L.8
Shendure, J.9
Eichler, E.E.10
-
17
-
-
33846614650
-
A high-resolution map of segmental DNA copy number variation in the mouse genome
-
10.1371/journal.pgen.0030003, 1761046, 17206864
-
Graubert TA, Cahan P, Edwin D, Selzer RR, Richmond TA, Eis PS, Shannon WD, Li X, McLeod HL, Cheverud JM. A high-resolution map of segmental DNA copy number variation in the mouse genome. PLoS Genet 2007, 3(1):e3. 10.1371/journal.pgen.0030003, 1761046, 17206864.
-
(2007)
PLoS Genet
, vol.3
, Issue.1
-
-
Graubert, T.A.1
Cahan, P.2
Edwin, D.3
Selzer, R.R.4
Richmond, T.A.5
Eis, P.S.6
Shannon, W.D.7
Li, X.8
McLeod, H.L.9
Cheverud, J.M.10
-
18
-
-
46249114293
-
Mouse segmental duplication and copy number variation
-
10.1038/ng.172, 2574762, 18500340
-
She X, Cheng Z, Zollner S, Church DM, Eichler EE. Mouse segmental duplication and copy number variation. Nat Genet 2008, 40(7):909-914. 10.1038/ng.172, 2574762, 18500340.
-
(2008)
Nat Genet
, vol.40
, Issue.7
, pp. 909-914
-
-
She, X.1
Cheng, Z.2
Zollner, S.3
Church, D.M.4
Eichler, E.E.5
-
19
-
-
38049055222
-
Genomic copy number and expression variation within the C57BL/6J inbred mouse strain
-
2134784, 18032724
-
Watkins-Chow DE, Pavan WJ. Genomic copy number and expression variation within the C57BL/6J inbred mouse strain. Genome Res 2008, 18(1):60-66. 2134784, 18032724.
-
(2008)
Genome Res
, vol.18
, Issue.1
, pp. 60-66
-
-
Watkins-Chow, D.E.1
Pavan, W.J.2
-
20
-
-
46249105777
-
Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster
-
10.1126/science.1158078, 18535209
-
Emerson JJ, Cardoso-Moreira M, Borevitz JO, Long M. Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster. Science 2008, 320(5883):1629-1631. 10.1126/science.1158078, 18535209.
-
(2008)
Science
, vol.320
, Issue.5883
, pp. 1629-1631
-
-
Emerson, J.J.1
Cardoso-Moreira, M.2
Borevitz, J.O.3
Long, M.4
-
21
-
-
84862529082
-
A genome-wide detection of copy number variations using SNP genotyping arrays in swine
-
10.1186/1471-2164-13-273, 3464621, 22726314
-
Wang J, Jiang J, Fu W, Jiang L, Ding X, Liu JF, Zhang Q. A genome-wide detection of copy number variations using SNP genotyping arrays in swine. BMC Genomics 2012, 13:273. 10.1186/1471-2164-13-273, 3464621, 22726314.
-
(2012)
BMC Genomics
, vol.13
, pp. 273
-
-
Wang, J.1
Jiang, J.2
Fu, W.3
Jiang, L.4
Ding, X.5
Liu, J.F.6
Zhang, Q.7
-
22
-
-
58049191440
-
A snapshot of CNVs in the pig genome
-
10.1371/journal.pone.0003916, 2596487, 19079605
-
Fadista J, Nygaard M, Holm LE, Thomsen B, Bendixen C. A snapshot of CNVs in the pig genome. PLoS One 2008, 3(12):e3916. 10.1371/journal.pone.0003916, 2596487, 19079605.
-
(2008)
PLoS One
, vol.3
, Issue.12
-
-
Fadista, J.1
Nygaard, M.2
Holm, L.E.3
Thomsen, B.4
Bendixen, C.5
-
23
-
-
77950637626
-
Identification of copy number variations and common deletion polymorphisms in cattle
-
10.1186/1471-2164-11-232, 2859865, 20377913
-
Bae JS, Cheong HS, Kim LH, NamGung S, Park TJ, Chun JY, Kim JY, Pasaje CF, Lee JS, Shin HD. Identification of copy number variations and common deletion polymorphisms in cattle. BMC Genomics 2010, 11:232. 10.1186/1471-2164-11-232, 2859865, 20377913.
-
(2010)
BMC Genomics
, vol.11
, pp. 232
-
-
Bae, J.S.1
Cheong, H.S.2
Kim, L.H.3
NamGung, S.4
Park, T.J.5
Chun, J.Y.6
Kim, J.Y.7
Pasaje, C.F.8
Lee, J.S.9
Shin, H.D.10
-
24
-
-
77951798133
-
Analysis of copy number variations among diverse cattle breeds
-
10.1101/gr.105403.110, 2860171, 20212021
-
Liu GE, Hou Y, Zhu B, Cardone MF, Jiang L, Cellamare A, Mitra A, Alexander LJ, Coutinho LL, Dell'Aquila ME. Analysis of copy number variations among diverse cattle breeds. Genome Res 2010, 20(5):693-703. 10.1101/gr.105403.110, 2860171, 20212021.
-
(2010)
Genome Res
, vol.20
, Issue.5
, pp. 693-703
-
-
Liu, G.E.1
Hou, Y.2
Zhu, B.3
Cardone, M.F.4
Jiang, L.5
Cellamare, A.6
Mitra, A.7
Alexander, L.J.8
Coutinho, L.L.9
Dell'Aquila, M.E.10
-
25
-
-
77951840186
-
Copy number variation in the bovine genome
-
10.1186/1471-2164-11-284, 2902221, 20459598
-
Fadista J, Thomsen B, Holm LE, Bendixen C. Copy number variation in the bovine genome. BMC Genomics 2010, 11:284. 10.1186/1471-2164-11-284, 2902221, 20459598.
-
(2010)
BMC Genomics
, vol.11
, pp. 284
-
-
Fadista, J.1
Thomsen, B.2
Holm, L.E.3
Bendixen, C.4
-
26
-
-
79951849727
-
Genomic characteristics of cattle copy number variations
-
10.1186/1471-2164-12-127, 3053260, 21345189
-
Hou Y, Liu GE, Bickhart DM, Cardone MF, Wang K, Kim ES, Matukumalli LK, Ventura M, Song J, VanRaden PM. Genomic characteristics of cattle copy number variations. BMC Genomics 2011, 12:127. 10.1186/1471-2164-12-127, 3053260, 21345189.
-
(2011)
BMC Genomics
, vol.12
, pp. 127
-
-
Hou, Y.1
Liu, G.E.2
Bickhart, D.M.3
Cardone, M.F.4
Wang, K.5
Kim, E.S.6
Matukumalli, L.K.7
Ventura, M.8
Song, J.9
VanRaden, P.M.10
-
27
-
-
35648976118
-
The diploid genome sequence of an individual human
-
10.1371/journal.pbio.0050254, 1964779, 17803354
-
Levy S, Sutton G, Ng PC, Feuk L, Halpern AL, Walenz BP, Axelrod N, Huang J, Kirkness EF, Denisov G. The diploid genome sequence of an individual human. PLoS Biol 2007, 5(10):e254. 10.1371/journal.pbio.0050254, 1964779, 17803354.
-
(2007)
PLoS Biol
, vol.5
, Issue.10
-
-
Levy, S.1
Sutton, G.2
Ng, P.C.3
Feuk, L.4
Halpern, A.L.5
Walenz, B.P.6
Axelrod, N.7
Huang, J.8
Kirkness, E.F.9
Denisov, G.10
-
28
-
-
67449106767
-
DNA copy number variation and gene expression analyses reveal the implication of specific oncogenes and genes in GBM
-
10.1080/07357900802563044, 19219654
-
Margareto J, Leis O, Larrarte E, Pomposo IC, Garibi JM, Lafuente JV. DNA copy number variation and gene expression analyses reveal the implication of specific oncogenes and genes in GBM. Cancer Invest 2009, 27(5):541-548. 10.1080/07357900802563044, 19219654.
-
(2009)
Cancer Invest
, vol.27
, Issue.5
, pp. 541-548
-
-
Margareto, J.1
Leis, O.2
Larrarte, E.3
Pomposo, I.C.4
Garibi, J.M.5
Lafuente, J.V.6
-
29
-
-
33846978695
-
Relative impact of nucleotide and copy number variation on gene expression phenotypes
-
10.1126/science.1136678, 2665772, 17289997
-
Stranger BE, Forrest MS, Dunning M, Ingle CE, Beazley C, Thorne N, Redon R, Bird CP, de Grassi A, Lee C. Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science 2007, 315(5813):848-853. 10.1126/science.1136678, 2665772, 17289997.
-
(2007)
Science
, vol.315
, Issue.5813
, pp. 848-853
-
-
Stranger, B.E.1
Forrest, M.S.2
Dunning, M.3
Ingle, C.E.4
Beazley, C.5
Thorne, N.6
Redon, R.7
Bird, C.P.8
de Grassi, A.9
Lee, C.10
-
30
-
-
70350221909
-
Copy number variation in human health, disease, and evolution
-
10.1146/annurev.genom.9.081307.164217, 19715442
-
Zhang F, Gu W, Hurles ME, Lupski JR. Copy number variation in human health, disease, and evolution. Annu Rev Genomics Hum Genet 2009, 10:451-481. 10.1146/annurev.genom.9.081307.164217, 19715442.
-
(2009)
Annu Rev Genomics Hum Genet
, vol.10
, pp. 451-481
-
-
Zhang, F.1
Gu, W.2
Hurles, M.E.3
Lupski, J.R.4
-
31
-
-
32844460938
-
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
-
10.1038/nature04489, 16482158
-
Aitman TJ, Dong R, Vyse TJ, Norsworthy PJ, Johnson MD, Smith J, Mangion J, Roberton-Lowe C, Marshall AJ, Petretto E. Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Nature 2006, 439(7078):851-855. 10.1038/nature04489, 16482158.
-
(2006)
Nature
, vol.439
, Issue.7078
, pp. 851-855
-
-
Aitman, T.J.1
Dong, R.2
Vyse, T.J.3
Norsworthy, P.J.4
Johnson, M.D.5
Smith, J.6
Mangion, J.7
Roberton-Lowe, C.8
Marshall, A.J.9
Petretto, E.10
-
32
-
-
80052260252
-
A copy number variation morbidity map of developmental delay
-
10.1038/ng.909, 3171215, 21841781
-
Cooper GM, Coe BP, Girirajan S, Rosenfeld JA, Vu TH, Baker C, Williams C, Stalker H, Hamid R, Hannig V. A copy number variation morbidity map of developmental delay. Nat Genet 2011, 43(9):838-846. 10.1038/ng.909, 3171215, 21841781.
-
(2011)
Nat Genet
, vol.43
, Issue.9
, pp. 838-846
-
-
Cooper, G.M.1
Coe, B.P.2
Girirajan, S.3
Rosenfeld, J.A.4
Vu, T.H.5
Baker, C.6
Williams, C.7
Stalker, H.8
Hamid, R.9
Hannig, V.10
-
33
-
-
34250841166
-
Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans
-
10.1086/518257, 1867093, 17503323
-
Yang Y, Chung EK, Wu YL, Savelli SL, Nagaraja HN, Zhou B, Hebert M, Jones KN, Shu Y, Kitzmiller K. Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans. Am J Hum Genet 2007, 80(6):1037-1054. 10.1086/518257, 1867093, 17503323.
-
(2007)
Am J Hum Genet
, vol.80
, Issue.6
, pp. 1037-1054
-
-
Yang, Y.1
Chung, E.K.2
Wu, Y.L.3
Savelli, S.L.4
Nagaraja, H.N.5
Zhou, B.6
Hebert, M.7
Jones, K.N.8
Shu, Y.9
Kitzmiller, K.10
-
34
-
-
67649289900
-
Copy number variation at 1q21.1 associated with neuroblastoma
-
10.1038/nature08035, 2755253, 19536264
-
Diskin SJ, Hou C, Glessner JT, Attiyeh EF, Laudenslager M, Bosse K, Cole K, Mosse YP, Wood A, Lynch JE. Copy number variation at 1q21.1 associated with neuroblastoma. Nature 2009, 459(7249):987-991. 10.1038/nature08035, 2755253, 19536264.
-
(2009)
Nature
, vol.459
, Issue.7249
, 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
Mosse, Y.P.8
Wood, A.9
Lynch, J.E.10
-
35
-
-
77949831756
-
Structural variation in the human genome and its role in disease
-
10.1146/annurev-med-100708-204735, 20059347
-
Stankiewicz P, Lupski JR. Structural variation in the human genome and its role in disease. Annu Rev Med 2010, 61:437-455. 10.1146/annurev-med-100708-204735, 20059347.
-
(2010)
Annu Rev Med
, vol.61
, pp. 437-455
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
36
-
-
80755187820
-
Human copy number variation and complex genetic disease
-
10.1146/annurev-genet-102209-163544, 21854229
-
Girirajan S, Campbell CD, Eichler EE. Human copy number variation and complex genetic disease. Annu Rev Genet 2011, 45:203-226. 10.1146/annurev-genet-102209-163544, 21854229.
-
(2011)
Annu Rev Genet
, vol.45
, pp. 203-226
-
-
Girirajan, S.1
Campbell, C.D.2
Eichler, E.E.3
-
37
-
-
67651219230
-
Copy number variation in intron 1 of SOX5 causes the Pea-comb phenotype in chickens
-
10.1371/journal.pgen.1000512, 2685452, 19521496
-
Wright D, Boije H, Meadows JR, Bed'hom B, Gourichon D, Vieaud A, Tixier-Boichard M, Rubin CJ, Imsland F, Hallbook F. Copy number variation in intron 1 of SOX5 causes the Pea-comb phenotype in chickens. PLoS Genet 2009, 5(6):e1000512. 10.1371/journal.pgen.1000512, 2685452, 19521496.
-
(2009)
PLoS Genet
, vol.5
, Issue.6
-
-
Wright, D.1
Boije, H.2
Meadows, J.R.3
Bed'hom, B.4
Gourichon, D.5
Vieaud, A.6
Tixier-Boichard, M.7
Rubin, C.J.8
Imsland, F.9
Hallbook, F.10
-
38
-
-
0036801609
-
A large duplication associated with dominant white color in pigs originated by homologous recombination between LINE elements flanking KIT
-
10.1007/s00335-002-2184-5, 12420135
-
Giuffra E, Tornsten A, Marklund S, Bongcam-Rudloff E, Chardon P, Kijas JM, Anderson SI, Archibald AL, Andersson L. A large duplication associated with dominant white color in pigs originated by homologous recombination between LINE elements flanking KIT. Mamm Genome 2002, 13(10):569-577. 10.1007/s00335-002-2184-5, 12420135.
-
(2002)
Mamm Genome
, vol.13
, Issue.10
, pp. 569-577
-
-
Giuffra, E.1
Tornsten, A.2
Marklund, S.3
Bongcam-Rudloff, E.4
Chardon, P.5
Kijas, J.M.6
Anderson, S.I.7
Archibald, A.L.8
Andersson, L.9
-
39
-
-
75749135275
-
Copy number variation and missense mutations of the agouti signaling protein (ASIP) gene in goat breeds with different coat colors
-
10.1159/000268089, 20016133
-
Fontanesi L, Beretti F, Riggio V, Gomez Gonzalez E, Dall'Olio S, Davoli R, Russo V, Portolano B. Copy number variation and missense mutations of the agouti signaling protein (ASIP) gene in goat breeds with different coat colors. Cytogenet Genome Res 2009, 126(4):333-347. 10.1159/000268089, 20016133.
-
(2009)
Cytogenet Genome Res
, vol.126
, Issue.4
, pp. 333-347
-
-
Fontanesi, L.1
Beretti, F.2
Riggio, V.3
Gomez Gonzalez, E.4
Dall'Olio, S.5
Davoli, R.6
Russo, V.7
Portolano, B.8
-
40
-
-
35349010252
-
Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs
-
10.1038/ng.2007.4, 17906623
-
Salmon Hillbertz NH, Isaksson M, Karlsson EK, Hellmen E, Pielberg GR, Savolainen P, Wade CM, von Euler H, Gustafson U, Hedhammar A. Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs. Nat Genet 2007, 39(11):1318-1320. 10.1038/ng.2007.4, 17906623.
-
(2007)
Nat Genet
, vol.39
, Issue.11
, pp. 1318-1320
-
-
Salmon Hillbertz, N.H.1
Isaksson, M.2
Karlsson, E.K.3
Hellmen, E.4
Pielberg, G.R.5
Savolainen, P.6
Wade, C.M.7
von Euler, H.8
Gustafson, U.9
Hedhammar, A.10
-
41
-
-
77955621176
-
An ADAM9 mutation in canine cone-rod dystrophy 3 establishes homology with human cone-rod dystrophy 9
-
2925905, 20806078
-
Goldstein O, Mezey JG, Boyko AR, Gao C, Wang W, Bustamante CD, Anguish LJ, Jordan JA, Pearce-Kelling SE, Aguirre GD. An ADAM9 mutation in canine cone-rod dystrophy 3 establishes homology with human cone-rod dystrophy 9. Mol Vis 2010, 16:1549-1569. 2925905, 20806078.
-
(2010)
Mol Vis
, vol.16
, pp. 1549-1569
-
-
Goldstein, O.1
Mezey, J.G.2
Boyko, A.R.3
Gao, C.4
Wang, W.5
Bustamante, C.D.6
Anguish, L.J.7
Jordan, J.A.8
Pearce-Kelling, S.E.9
Aguirre, G.D.10
-
42
-
-
79955975154
-
Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene
-
10.1016/j.nbd.2011.03.010, 21420493
-
Gill JL, Capper D, Vanbellinghen JF, Chung SK, Higgins RJ, Rees MI, Shelton GD, Harvey RJ. Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene. Neurobiol Dis 2011, 43(1):184-189. 10.1016/j.nbd.2011.03.010, 21420493.
-
(2011)
Neurobiol Dis
, vol.43
, Issue.1
, pp. 184-189
-
-
Gill, J.L.1
Capper, D.2
Vanbellinghen, J.F.3
Chung, S.K.4
Higgins, R.J.5
Rees, M.I.6
Shelton, G.D.7
Harvey, R.J.8
-
43
-
-
77952726398
-
A deletion mutation in bovine SLC4A2 is associated with osteopetrosis in Red Angus cattle
-
10.1186/1471-2164-11-337, 2891616, 20507629
-
Meyers SN, McDaneld TG, Swist SL, Marron BM, Steffen DJ, O'Toole D, O'Connell JR, Beever JE, Sonstegard TS, Smith TP. A deletion mutation in bovine SLC4A2 is associated with osteopetrosis in Red Angus cattle. BMC Genomics 2010, 11:337. 10.1186/1471-2164-11-337, 2891616, 20507629.
-
(2010)
BMC Genomics
, vol.11
, pp. 337
-
-
Meyers, S.N.1
McDaneld, T.G.2
Swist, S.L.3
Marron, B.M.4
Steffen, D.J.5
O'Toole, D.6
O'Connell, J.R.7
Beever, J.E.8
Sonstegard, T.S.9
Smith, T.P.10
-
44
-
-
78649771224
-
A novel mutation in the maternally imprinted PEG3 domain results in a loss of MIMT1 expression and causes abortions and stillbirths in cattle (Bos taurus)
-
10.1371/journal.pone.0015116, 2994898, 21152099
-
Flisikowski K, Venhoranta H, Nowacka-Woszuk J, McKay SD, Flyckt A, Taponen J, Schnabel R, Schwarzenbacher H, Szczerbal I, Lohi H. A novel mutation in the maternally imprinted PEG3 domain results in a loss of MIMT1 expression and causes abortions and stillbirths in cattle (Bos taurus). PLoS One 2010, 5(11):e15116. 10.1371/journal.pone.0015116, 2994898, 21152099.
-
(2010)
PLoS One
, vol.5
, Issue.11
-
-
Flisikowski, K.1
Venhoranta, H.2
Nowacka-Woszuk, J.3
McKay, S.D.4
Flyckt, A.5
Taponen, J.6
Schnabel, R.7
Schwarzenbacher, H.8
Szczerbal, I.9
Lohi, H.10
-
45
-
-
78649351737
-
Analysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPs
-
10.1186/1471-2164-11-673, 3091787, 21114805
-
Seroussi E, Glick G, Shirak A, Yakobson E, Weller JI, Ezra E, Zeron Y. Analysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPs. BMC Genomics 2010, 11:673. 10.1186/1471-2164-11-673, 3091787, 21114805.
-
(2010)
BMC Genomics
, vol.11
, pp. 673
-
-
Seroussi, E.1
Glick, G.2
Shirak, A.3
Yakobson, E.4
Weller, J.I.5
Ezra, E.6
Zeron, Y.7
-
46
-
-
33751345434
-
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
-
10.1101/gr.5629106, 1665641, 17122084
-
Komura D, Shen F, Ishikawa S, Fitch KR, Chen W, Zhang J, Liu G, Ihara S, Nakamura H, Hurles ME. Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays. Genome Res 2006, 16(12):1575-1584. 10.1101/gr.5629106, 1665641, 17122084.
-
(2006)
Genome Res
, vol.16
, Issue.12
, pp. 1575-1584
-
-
Komura, D.1
Shen, F.2
Ishikawa, S.3
Fitch, K.R.4
Chen, W.5
Zhang, J.6
Liu, G.7
Ihara, S.8
Nakamura, H.9
Hurles, M.E.10
-
47
-
-
35748971743
-
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases
-
10.1093/hmg/ddm208, 17666407
-
de Smith AJ, Tsalenko A, Sampas N, Scheffer A, Yamada NA, Tsang P, Ben-Dor A, Yakhini Z, Ellis RJ, Bruhn L. Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases. Hum Mol Genet 2007, 16(23):2783-2794. 10.1093/hmg/ddm208, 17666407.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.23
, pp. 2783-2794
-
-
de Smith, A.J.1
Tsalenko, A.2
Sampas, N.3
Scheffer, A.4
Yamada, N.A.5
Tsang, P.6
Ben-Dor, A.7
Yakhini, Z.8
Ellis, R.J.9
Bruhn, L.10
-
48
-
-
52249106010
-
Comparison of the Agilent
-
Baumbusch LO, Aaroe J, Johansen FE, Hicks J, Sun H, Bruhn L, Gunderson K, Naume B, Kristensen VN, Liestol K. Comparison of the Agilent. ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors. BMC Genomics 2008, 9:379.
-
(2008)
ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors. BMC Genomics
, vol.9
, pp. 379
-
-
Baumbusch, L.O.1
Aaroe, J.2
Johansen, F.E.3
Hicks, J.4
Sun, H.5
Bruhn, L.6
Gunderson, K.7
Naume, B.8
Kristensen, V.N.9
Liestol, K.10
-
49
-
-
10844232112
-
Whole genome DNA copy number changes identified by high density oligonucleotide arrays
-
10.1186/1479-7364-1-4-287, 15588488
-
Huang J, Wei W, Zhang J, Liu G, Bignell GR, Stratton MR, Futreal PA, Wooster R, Jones KW, Shapero MH. Whole genome DNA copy number changes identified by high density oligonucleotide arrays. Hum Genomics 2004, 1(4):287-299. 10.1186/1479-7364-1-4-287, 15588488.
-
(2004)
Hum Genomics
, vol.1
, Issue.4
, pp. 287-299
-
-
Huang, J.1
Wei, W.2
Zhang, J.3
Liu, G.4
Bignell, G.R.5
Stratton, M.R.6
Futreal, P.A.7
Wooster, R.8
Jones, K.W.9
Shapero, M.H.10
-
50
-
-
62549137441
-
CNV discovery using SNP genotyping arrays
-
Yau C, Holmes CC. CNV discovery using SNP genotyping arrays. Cytogenet Genome Res 2008, 123(1-4):307-312.
-
(2008)
Cytogenet Genome Res
, vol.123
, Issue.1-4
, pp. 307-312
-
-
Yau, C.1
Holmes, C.C.2
-
51
-
-
57149102071
-
Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis
-
10.1016/j.ygeno.2008.08.012, 2631358, 18822366
-
Ionita-Laza I, Rogers AJ, Lange C, Raby BA, Lee C. Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis. Genomics 2009, 93(1):22-26. 10.1016/j.ygeno.2008.08.012, 2631358, 18822366.
-
(2009)
Genomics
, vol.93
, Issue.1
, pp. 22-26
-
-
Ionita-Laza, I.1
Rogers, A.J.2
Lange, C.3
Raby, B.A.4
Lee, C.5
-
52
-
-
73449095762
-
The pitfalls of platform comparison: DNA copy number array technologies assessed
-
10.1186/1471-2164-10-588, 2797821, 19995423
-
Curtis C, Lynch AG, Dunning MJ, Spiteri I, Marioni JC, Hadfield J, Chin SF, Brenton JD, Tavare S, Caldas C. The pitfalls of platform comparison: DNA copy number array technologies assessed. BMC Genomics 2009, 10:588. 10.1186/1471-2164-10-588, 2797821, 19995423.
-
(2009)
BMC Genomics
, vol.10
, pp. 588
-
-
Curtis, C.1
Lynch, A.G.2
Dunning, M.J.3
Spiteri, I.4
Marioni, J.C.5
Hadfield, J.6
Chin, S.F.7
Brenton, J.D.8
Tavare, S.9
Caldas, C.10
-
53
-
-
54949156063
-
Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios
-
10.1186/1471-2105-9-409, 2572624, 18831757
-
Staaf J, Vallon-Christersson J, Lindgren D, Juliusson G, Rosenquist R, Hoglund M, Borg A, Ringner M. Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios. BMC Bioinformatics 2008, 9:409. 10.1186/1471-2105-9-409, 2572624, 18831757.
-
(2008)
BMC Bioinformatics
, vol.9
, pp. 409
-
-
Staaf, J.1
Vallon-Christersson, J.2
Lindgren, D.3
Juliusson, G.4
Rosenquist, R.5
Hoglund, M.6
Borg, A.7
Ringner, M.8
-
54
-
-
70350004083
-
Comparing CNV detection methods for SNP arrays
-
10.1093/bfgp/elp017, 19737800
-
Winchester L, Yau C, Ragoussis J. Comparing CNV detection methods for SNP arrays. Brief Funct Genomic Proteomic 2009, 8(5):353-366. 10.1093/bfgp/elp017, 19737800.
-
(2009)
Brief Funct Genomic Proteomic
, vol.8
, Issue.5
, pp. 353-366
-
-
Winchester, L.1
Yau, C.2
Ragoussis, J.3
-
55
-
-
84864521942
-
Fine mapping of copy number variations on two cattle genome assemblies using high density SNP array
-
10.1186/1471-2164-13-376, 3583728, 22866901
-
Hou Y, Bickhart DM, Hvinden ML, Li C, Song J, Boichard DA, Fritz S, Eggen A, Denise S, Wiggans GR. Fine mapping of copy number variations on two cattle genome assemblies using high density SNP array. BMC Genomics 2012, 13(1):376. 10.1186/1471-2164-13-376, 3583728, 22866901.
-
(2012)
BMC Genomics
, vol.13
, Issue.1
, pp. 376
-
-
Hou, Y.1
Bickhart, D.M.2
Hvinden, M.L.3
Li, C.4
Song, J.5
Boichard, D.A.6
Fritz, S.7
Eggen, A.8
Denise, S.9
Wiggans, G.R.10
-
56
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
10.1038/nature07953, 2925224, 19404257
-
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009, 459(7246):569-573. 10.1038/nature07953, 2925224, 19404257.
-
(2009)
Nature
, vol.459
, Issue.7246
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
Korvatska, O.4
Kim, C.E.5
Wood, S.6
Zhang, H.7
Estes, A.8
Brune, C.W.9
Bradfield, J.P.10
-
57
-
-
79551581823
-
Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study
-
10.1002/humu.21398, 3230937, 21089066
-
Marenne G, Rodriguez-Santiago B, Closas MG, Perez-Jurado L, Rothman N, Rico D, Pita G, Pisano DG, Kogevinas M, Silverman DT. Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study. Hum Mutat 2011, 32(2):240-248. 10.1002/humu.21398, 3230937, 21089066.
-
(2011)
Hum Mutat
, vol.32
, Issue.2
, pp. 240-248
-
-
Marenne, G.1
Rodriguez-Santiago, B.2
Closas, M.G.3
Perez-Jurado, L.4
Rothman, N.5
Rico, D.6
Pita, G.7
Pisano, D.G.8
Kogevinas, M.9
Silverman, D.T.10
-
58
-
-
84858442084
-
Genomic regions showing copy number variations associate with resistance or susceptibility to gastrointestinal nematodes in Angus cattle
-
10.1007/s10142-011-0252-1, 21928070
-
Hou Y, Liu GE, Bickhart DM, Matukumalli LK, Li C, Song J, Gasbarre LC, Van Tassell CP, Sonstegard TS. Genomic regions showing copy number variations associate with resistance or susceptibility to gastrointestinal nematodes in Angus cattle. Funct Integr Genomics 2012, 12(1):81-92. 10.1007/s10142-011-0252-1, 21928070.
-
(2012)
Funct Integr Genomics
, vol.12
, Issue.1
, pp. 81-92
-
-
Hou, Y.1
Liu, G.E.2
Bickhart, D.M.3
Matukumalli, L.K.4
Li, C.5
Song, J.6
Gasbarre, L.C.7
Van Tassell, C.P.8
Sonstegard, T.S.9
-
59
-
-
75549089967
-
The UCSC Genome Browser database: update 2010
-
Rhead B, Karolchik D, Kuhn RM, Hinrichs AS, Zweig AS, Fujita PA, Diekhans M, Smith KE, Rosenbloom KR, Raney BJ. The UCSC Genome Browser database: update 2010. Nucleic Acids Res 2010, 38(Database issue):613-619.
-
(2010)
Nucleic Acids Res
, vol.38
, Issue.DATABASE ISSUE
, pp. 613-619
-
-
Rhead, B.1
Karolchik, D.2
Kuhn, R.M.3
Hinrichs, A.S.4
Zweig, A.S.5
Fujita, P.A.6
Diekhans, M.7
Smith, K.E.8
Rosenbloom, K.R.9
Raney, B.J.10
-
60
-
-
84868688073
-
Genome-wide identification of copy number variations in Chinese Holstein
-
10.1371/journal.pone.0048732, 3492429, 23144949
-
Jiang L, Jiang J, Wang J, Ding X, Liu J, Zhang Q. Genome-wide identification of copy number variations in Chinese Holstein. PLoS One 2012, 7(11):e48732. 10.1371/journal.pone.0048732, 3492429, 23144949.
-
(2012)
PLoS One
, vol.7
, Issue.11
-
-
Jiang, L.1
Jiang, J.2
Wang, J.3
Ding, X.4
Liu, J.5
Zhang, Q.6
-
61
-
-
61849144443
-
The genomic architecture of segmental duplications and associated copy number variants in dogs
-
2661811, 19129542
-
Nicholas TJ, Cheng Z, Ventura M, Mealey K, Eichler EE, Akey JM. The genomic architecture of segmental duplications and associated copy number variants in dogs. Genome Res 2009, 19(3):491-499. 2661811, 19129542.
-
(2009)
Genome Res
, vol.19
, Issue.3
, pp. 491-499
-
-
Nicholas, T.J.1
Cheng, Z.2
Ventura, M.3
Mealey, K.4
Eichler, E.E.5
Akey, J.M.6
-
62
-
-
35948984173
-
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
-
10.1101/gr.6861907, 2045149, 17921354
-
Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, Hakonarson H, Bucan M. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 2007, 17(11):1665-1674. 10.1101/gr.6861907, 2045149, 17921354.
-
(2007)
Genome Res
, vol.17
, Issue.11
, pp. 1665-1674
-
-
Wang, K.1
Li, M.2
Hadley, D.3
Liu, R.4
Glessner, J.5
Grant, S.F.6
Hakonarson, H.7
Bucan, M.8
-
63
-
-
65149096757
-
A whole-genome assembly of the domestic cow, Bos taurus
-
10.1186/gb-2009-10-4-r42, 2688933, 19393038
-
Zimin AV, Delcher AL, Florea L, Kelley DR, Schatz MC, Puiu D, Hanrahan F, Pertea G, Van Tassell CP, Sonstegard TS. A whole-genome assembly of the domestic cow, Bos taurus. Genome Biol 2009, 10(4):R42. 10.1186/gb-2009-10-4-r42, 2688933, 19393038.
-
(2009)
Genome Biol
, vol.10
, Issue.4
-
-
Zimin, A.V.1
Delcher, A.L.2
Florea, L.3
Kelley, D.R.4
Schatz, M.C.5
Puiu, D.6
Hanrahan, F.7
Pertea, G.8
Van Tassell, C.P.9
Sonstegard, T.S.10
-
64
-
-
39749197456
-
Genotype, haplotype and copy-number variation in worldwide human populations
-
10.1038/nature06742, 18288195
-
Jakobsson M, Scholz SW, Scheet P, Gibbs JR, VanLiere JM, Fung HC, Szpiech ZA, Degnan JH, Wang K, Guerreiro R. Genotype, haplotype and copy-number variation in worldwide human populations. Nature 2008, 451(7181):998-1003. 10.1038/nature06742, 18288195.
-
(2008)
Nature
, vol.451
, Issue.7181
, pp. 998-1003
-
-
Jakobsson, M.1
Scholz, S.W.2
Scheet, P.3
Gibbs, J.R.4
VanLiere, J.M.5
Fung, H.C.6
Szpiech, Z.A.7
Degnan, J.H.8
Wang, K.9
Guerreiro, R.10
-
65
-
-
77953776675
-
Strong synaptic transmission impact by copy number variations in schizophrenia
-
10.1073/pnas.1000274107, 2890845, 20489179
-
Glessner JT, Reilly MP, Kim CE, Takahashi N, Albano A, Hou C, Bradfield JP, Zhang H, Sleiman PM, Flory JH. Strong synaptic transmission impact by copy number variations in schizophrenia. Proc Natl Acad Sci U S A 2010, 107(23):10584-10589. 10.1073/pnas.1000274107, 2890845, 20489179.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, Issue.23
, pp. 10584-10589
-
-
Glessner, J.T.1
Reilly, M.P.2
Kim, C.E.3
Takahashi, N.4
Albano, A.5
Hou, C.6
Bradfield, J.P.7
Zhang, H.8
Sleiman, P.M.9
Flory, J.H.10
-
66
-
-
0034069495
-
Gene ontology: tool for the unification of biology. The Gene Ontology Consortium
-
10.1038/75556, 3037419, 10802651
-
Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS, Eppig JT. Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet 2000, 25(1):25-29. 10.1038/75556, 3037419, 10802651.
-
(2000)
Nat Genet
, vol.25
, Issue.1
, pp. 25-29
-
-
Ashburner, M.1
Ball, C.A.2
Blake, J.A.3
Botstein, D.4
Butler, H.5
Cherry, J.M.6
Davis, A.P.7
Dolinski, K.8
Dwight, S.S.9
Eppig, J.T.10
-
67
-
-
75549090213
-
KEGG for representation and analysis of molecular networks involving diseases and drugs
-
Kanehisa M, Goto S, Furumichi M, Tanabe M, Hirakawa M. KEGG for representation and analysis of molecular networks involving diseases and drugs. Nucleic Acids Res 2010, 38(Database issue):355-360.
-
(2010)
Nucleic Acids Res
, vol.38
, Issue.DATABASE ISSUE
, pp. 355-360
-
-
Kanehisa, M.1
Goto, S.2
Furumichi, M.3
Tanabe, M.4
Hirakawa, M.5
-
68
-
-
61449172037
-
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
-
da Huang W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc 2009, 4(1):44-57.
-
(2009)
Nat Protoc
, vol.4
, Issue.1
, pp. 44-57
-
-
da Huang, W.1
Sherman, B.T.2
Lempicki, R.A.3
-
69
-
-
31044436017
-
Determination of cytochrome P450 2D6 (CYP2D6) gene copy number by real-time quantitative PCR
-
10.1155/JBB.2005.248, 1224698, 16192683
-
Bodin L, Beaune PH, Loriot MA. Determination of cytochrome P450 2D6 (CYP2D6) gene copy number by real-time quantitative PCR. J Biomed Biotechnol 2005, 2005(3):248-253. 10.1155/JBB.2005.248, 1224698, 16192683.
-
(2005)
J Biomed Biotechnol
, vol.2005
, Issue.3
, pp. 248-253
-
-
Bodin, L.1
Beaune, P.H.2
Loriot, M.A.3
-
70
-
-
77649232260
-
Accurate and objective copy number profiling using real-time quantitative PCR
-
10.1016/j.ymeth.2009.12.007, 20060046
-
D'Haene B, Vandesompele J, Hellemans J. Accurate and objective copy number profiling using real-time quantitative PCR. Methods 2010, 50(4):262-270. 10.1016/j.ymeth.2009.12.007, 20060046.
-
(2010)
Methods
, vol.50
, Issue.4
, pp. 262-270
-
-
D'Haene, B.1
Vandesompele, J.2
Hellemans, J.3
|