-
1
-
-
72149083621
-
Mapping human genetic diversity in Asia
-
Abdulla MA, Ahmed I, Assawamakin A, Bhak J, Brahmachari SK, Calacal GC, Chaurasia A, Chen CH, Chen J, Chen YT, and others. 2009. Mapping human genetic diversity in Asia. Science 326:1541-1545.
-
(2009)
Science
, vol.326
, pp. 1541-1545
-
-
Abdulla, M.A.1
Ahmed, I.2
Assawamakin, A.3
Bhak, J.4
Brahmachari, S.K.5
Calacal, G.C.6
Chaurasia, A.7
Chen, C.H.8
Chen, J.9
Chen, Y.T.10
-
2
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR. 2010. A method and server for predicting damaging missense mutations. Nat Methods 7:248-249.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
Kondrashov, A.S.7
Sunyaev, S.R.8
-
3
-
-
69749124820
-
The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group
-
Ahn SM, Kim TH, Lee S, Kim D, Ghang H, Kim DS, Kim BC, Kim SY, Kim WY, Kim C and others. 2009. The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group. Genome Res 19:1622-9.
-
(2009)
Genome Res
, vol.19
, pp. 1622-1629
-
-
Ahn, S.M.1
Kim, T.H.2
Lee, S.3
Kim, D.4
Ghang, H.5
Kim, D.S.6
Kim, B.C.7
Kim, S.Y.8
Kim, W.Y.9
Kim, C.10
-
4
-
-
34047182529
-
PharmGKB: a logical home for knowledge relating genotype to drug response phenotype
-
Altman RB. 2007. PharmGKB: a logical home for knowledge relating genotype to drug response phenotype. Nat Genet 39:426.
-
(2007)
Nat Genet
, vol.39
, pp. 426
-
-
Altman, R.B.1
-
6
-
-
17944370402
-
Genetic evidence on the origins of Indian caste populations
-
Bamshad M, Kivisild T, Watkins WS, Dixon ME, Ricker CE, Rao BB, Naidu JM, Prasad BV, Reddy PG, Rasanayagam A and others. 2001. Genetic evidence on the origins of Indian caste populations. Genome Res 11:994-1004.
-
(2001)
Genome Res
, vol.11
, pp. 994-1004
-
-
Bamshad, M.1
Kivisild, T.2
Watkins, W.S.3
Dixon, M.E.4
Ricker, C.E.5
Rao, B.B.6
Naidu, J.M.7
Prasad, B.V.8
Reddy, P.G.9
Rasanayagam, A.10
-
7
-
-
10744228209
-
Ethnic India: a genomic view, with special reference to peopling and structure
-
Basu A, Mukherjee N, Roy S, Sengupta S, Banerjee S, Chakraborty M, Dey B, Roy M, Roy B, Bhattacharyya NP and others. 2003. Ethnic India: a genomic view, with special reference to peopling and structure. Genome Res 13:2277-2290.
-
(2003)
Genome Res
, vol.13
, pp. 2277-2290
-
-
Basu, A.1
Mukherjee, N.2
Roy, S.3
Sengupta, S.4
Banerjee, S.5
Chakraborty, M.6
Dey, B.7
Roy, M.8
Roy, B.9
Bhattacharyya, N.P.10
-
8
-
-
79957622234
-
miRvar: a comprehensive database for genomic variations in microRNAs
-
Bhartiya D, Laddha SV, Mukhopadhyay A, Scaria V. 2011. miRvar: a comprehensive database for genomic variations in microRNAs. Hum Mutat 32:E2226-E2245.
-
(2011)
Hum Mutat
, vol.32
-
-
Bhartiya, D.1
Laddha, S.V.2
Mukhopadhyay, A.3
Scaria, V.4
-
9
-
-
69549116107
-
BreakDancer: an algorithm for high-resolution mapping of genomic structuralvariation
-
Chen K, Wallis JW, McLellan MD, Larson DE, Kalicki JM, Pohl CS, McGrath SD, Wendl MC, Zhang Q, Locke DP, Shi X, Fulton RS, Ley TJ, Wilson RK, Ding L, Mardis ER. BreakDancer: an algorithm for high-resolution mapping of genomic structuralvariation. Nat Methods 6:677-681.
-
Nat Methods
, vol.6
, pp. 677-681
-
-
Chen, K.1
Wallis, J.W.2
McLellan, M.D.3
Larson, D.E.4
Kalicki, J.M.5
Pohl, C.S.6
McGrath, S.D.7
Wendl, M.C.8
Zhang, Q.9
Locke, D.P.10
Shi, X.11
Fulton, R.S.12
Ley, T.J.13
Wilson, R.K.14
Ding, L.15
Mardis, E.R.16
-
10
-
-
77952574849
-
Uncovering the roles of rare variants in common disease through whole-genome sequencing
-
Cirulli ET, Goldstein DB. 2010. Uncovering the roles of rare variants in common disease through whole-genome sequencing 2009. Nat RevGenet 11:415-425.
-
(2010)
Nat RevGenet
, vol.11
, pp. 415-425
-
-
Cirulli, E.T.1
Goldstein, D.B.2
-
11
-
-
78049321495
-
Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing
-
Fujimoto A, Nakagawa H, Hosono N, Nakano K, Abe T, Boroevich KA, Nagasaki M, Yamaguchi R, Shibuya T, Kubo M and others. 2010. Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing. Nat Genet 42:931-936.
-
(2010)
Nat Genet
, vol.42
, pp. 931-936
-
-
Fujimoto, A.1
Nakagawa, H.2
Hosono, N.3
Nakano, K.4
Abe, T.5
Boroevich, K.A.6
Nagasaki, M.7
Yamaguchi, R.8
Shibuya, T.9
Kubo, M.10
-
15
-
-
38549122239
-
International genome project launched
-
Hayden EC. 2008. International genome project launched. Nature 451:378-379.
-
(2008)
Nature
, vol.451
, pp. 378-379
-
-
Hayden, E.C.1
-
16
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA. 2009. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA 106:9362-9367.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
Manolio, T.A.7
-
17
-
-
28044436937
-
The Indian Genome Variation database (IGVdb): a project overview
-
Indian Genome Variation Consortium 2005. The Indian Genome Variation database (IGVdb): a project overview. Hum Genet 118:1-11.
-
(2005)
Hum Genet
, vol.118
, pp. 1-11
-
-
Indian Genome Variation Consortium1
-
18
-
-
44149107150
-
Genetic landscape of the people of India: a canvas for disease gene exploration
-
Indian Genome Variation Consortium 2008. Genetic landscape of the people of India: a canvas for disease gene exploration. J Genet 87:3-20.
-
(2008)
J Genet
, vol.87
, pp. 3-20
-
-
Indian Genome Variation Consortium1
-
19
-
-
79959503826
-
The International HapMap Project
-
International HapMap Consortium 2003. The International HapMap Project. Nature 426:789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
International HapMap Consortium1
-
21
-
-
69249232047
-
A highly annotated whole-genome sequence of a Korean individual
-
Kim JI, Ju YS, Park H, Kim S, Lee S, Yi JH, Mudge J, Miller NA, Hong D, Bell CJ, and others. 2009. A highly annotated whole-genome sequence of a Korean individual. Nature 460:1011-1015.
-
(2009)
Nature
, vol.460
, pp. 1011-1015
-
-
Kim, J.I.1
Ju, Y.S.2
Park, H.3
Kim, S.4
Lee, S.5
Yi, J.H.6
Mudge, J.7
Miller, N.A.8
Hong, D.9
Bell, C.J.10
-
22
-
-
78651333227
-
Haplotype-resolved genome sequencing of a Gujarati Indian individual
-
Kitzman JO, Mackenzie AP, Adey A, Hiatt JB, Patwardhan RP, Sudmant PH, Ng SB, Alkan C, Qiu R, Eichler EE and others. 2011. Haplotype-resolved genome sequencing of a Gujarati Indian individual. Nat Biotechnol 29:59-63.
-
(2011)
Nat Biotechnol
, vol.29
, pp. 59-63
-
-
Kitzman, J.O.1
Mackenzie, A.P.2
Adey, A.3
Hiatt, J.B.4
Patwardhan, R.P.5
Sudmant, P.H.6
Ng, S.B.7
Alkan, C.8
Qiu, R.9
Eichler, E.E.10
-
23
-
-
78651293534
-
miRBase: integrating microRNA annotation and deep-sequencing data
-
Kozomara A, Griffiths-Jones S. 2011. miRBase: integrating microRNA annotation and deep-sequencing data. Nucleic Acids Res 39:D152-D157.
-
(2011)
Nucleic Acids Res
, vol.39
-
-
Kozomara, A.1
Griffiths-Jones, S.2
-
24
-
-
55549101623
-
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome
-
Ley TJ, Mardis ER, Ding L, Fulton B, McLellan MD, Chen K, Dooling D, Dunford-Shore BH, McGrath S, Hickenbotham M, and others. 2008. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature 456:66-72.
-
(2008)
Nature
, vol.456
, pp. 66-72
-
-
Ley, T.J.1
Mardis, E.R.2
Ding, L.3
Fulton, B.4
McLellan, M.D.5
Chen, K.6
Dooling, D.7
Dunford-Shore, B.H.8
McGrath, S.9
Hickenbotham, M.10
-
25
-
-
39649117755
-
The impact of next-generation sequencing technology on genetics
-
Mardis ER. 2008. The impact of next-generation sequencing technology on genetics. Trends Genet 24:133-141.
-
(2008)
Trends Genet
, vol.24
, pp. 133-141
-
-
Mardis, E.R.1
-
26
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis ER, Ding L, Dooling DJ, Larson DE, McLellan MD, Chen K, Koboldt DC, Fulton RS, Delehaunty KD, McGrath SD, and others. 2009. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med 361:1058-1066.
-
(2009)
N Engl J Med
, vol.361
, pp. 1058-1066
-
-
Mardis, E.R.1
Ding, L.2
Dooling, D.J.3
Larson, D.E.4
McLellan, M.D.5
Chen, K.6
Koboldt, D.C.7
Fulton, R.S.8
Delehaunty, K.D.9
McGrath, S.D.10
-
27
-
-
34249724360
-
Noncoding RNAs and RNA editing in brain development, functional diversification, and neurological disease
-
Mehler MF, Mattick JS. 2007. Noncoding RNAs and RNA editing in brain development, functional diversification, and neurological disease. Physiol Rev 87:799-823.
-
(2007)
Physiol Rev
, vol.87
, pp. 799-823
-
-
Mehler, M.F.1
Mattick, J.S.2
-
28
-
-
72849144434
-
Sequencing technologies-the next generation
-
Metzker ML. 2010. Sequencing technologies-the next generation. Nat RevGenet 11:31-46.
-
(2010)
Nat RevGenet
, vol.11
, pp. 31-46
-
-
Metzker, M.L.1
-
29
-
-
77956838065
-
Advances in understanding cancer genomes through second-generation sequencing
-
Meyerson M, Gabriel S, Getz G 2010. Advances in understanding cancer genomes through second-generation sequencing. Nat RevGenet 11:685-696.
-
(2010)
Nat RevGenet
, vol.11
, pp. 685-696
-
-
Meyerson, M.1
Gabriel, S.2
Getz, G.3
-
30
-
-
0035026704
-
Predicting deleterious amino acid substitutions
-
Ng PC, Henikoff S. Predicting deleterious amino acid substitutions. 2001. Genome Res 11:863-874.
-
(2001)
Genome Res
, vol.11
, pp. 863-874
-
-
Ng, P.C.1
Henikoff, S.2
-
31
-
-
70349472875
-
Reconstructing Indian population history
-
Reich D, Thangaraj K, Patterson N, Price AL, Singh L. 2009. Reconstructing Indian population history. Nature 461:489-494.
-
(2009)
Nature
, vol.461
, pp. 489-494
-
-
Reich, D.1
Thangaraj, K.2
Patterson, N.3
Price, A.L.4
Singh, L.5
-
32
-
-
0034816694
-
Genomic structures and population histories of linguistically distinct tribal groups of India
-
Roychoudhury S, Roy S, Basu A, Banerjee R, Vishwanathan H, Usha Rani MV, Sil SK, Mitra M, Majumder PP. 2001. Genomic structures and population histories of linguistically distinct tribal groups of India. Hum Genet 109:339-350.
-
(2001)
Hum Genet
, vol.109
, pp. 339-350
-
-
Roychoudhury, S.1
Roy, S.2
Basu, A.3
Banerjee, R.4
Vishwanathan, H.5
Usha Rani, M.V.6
Sil, S.K.7
Mitra, M.8
Majumder, P.P.9
-
33
-
-
37749031255
-
Next-generation sequencing transforms today's biology
-
Schuster SC. 2008. Next-generation sequencing transforms today's biology. Nat Methods 5:16-18.
-
(2008)
Nat Methods
, vol.5
, pp. 16-18
-
-
Schuster, S.C.1
-
34
-
-
53649106195
-
Next-generation DNA sequencing
-
Shendure J, Ji H. 2008. Next-generation DNA sequencing. Nat Biotechnol 26:1135-1145.
-
(2008)
Nat Biotechnol
, vol.26
, pp. 1135-1145
-
-
Shendure, J.1
Ji, H.2
-
35
-
-
0035173378
-
dbSNP: the NCBI database of genetic variation
-
Sherry ST, Ward MH, Kholodov M, Baker J, Phan L, Smigielski EM, Sirotkin K. 2001. dbSNP: the NCBI database of genetic variation. Nucleic Acids Res 29:308-311.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.H.2
Kholodov, M.3
Baker, J.4
Phan, L.5
Smigielski, E.M.6
Sirotkin, K.7
-
37
-
-
73949085491
-
Non-coding RNAs: regulators of disease
-
Taft RJ, Pang KC, Mercer TR, Dinger M, Mattick JS. 2010. Non-coding RNAs: regulators of disease. J Pathol 220:126-139.
-
(2010)
J Pathol
, vol.220
, pp. 126-139
-
-
Taft, R.J.1
Pang, K.C.2
Mercer, T.R.3
Dinger, M.4
Mattick, J.S.5
-
38
-
-
70350710156
-
Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations
-
Teo YY, Sim X, Ong RT, Tan AK, Chen J, Tantoso E, Small KS, Ku CS, Lee EJ, Seielstad M and others. 2009. Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations. Genome Res 19:2154-2162.
-
(2009)
Genome Res
, vol.19
, pp. 2154-2162
-
-
Teo, Y.Y.1
Sim, X.2
Ong, R.T.3
Tan, A.K.4
Chen, J.5
Tantoso, E.6
Small, K.S.7
Ku, C.S.8
Lee, E.J.9
Seielstad, M.10
-
39
-
-
68249092574
-
Massively parallel sequencing: the next big thing in genetic medicine
-
Tucker T, Marra M, Friedman JM. 2009. Massively parallel sequencing: the next big thing in genetic medicine. Am J Hum Genet 85:142-154.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 142-154
-
-
Tucker, T.1
Marra, M.2
Friedman, J.M.3
-
40
-
-
64149123778
-
Next-generation sequencing: from basic research to diagnostics
-
Voelkerding KV, Dames SA, Durtschi JD. 2009. Next-generation sequencing: from basic research to diagnostics. Clin Chem 55:641-658.
-
(2009)
Clin Chem
, vol.55
, pp. 641-658
-
-
Voelkerding, K.V.1
Dames, S.A.2
Durtschi, J.D.3
-
41
-
-
77956534324
-
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
-
Wang K, Li M, Hakonarson H. 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
Li, M.2
Hakonarson, H.3
-
42
-
-
55549097849
-
The diploid genome sequence of an Asian individual
-
Wang J, Wang W, Li R, Li Y, Tian G, Goodman L, Fan W, Zhang J, Li J, Guo Y, and others. 2008. The diploid genome sequence of an Asian individual. Nature 456:60-65.
-
(2008)
Nature
, vol.456
, pp. 60-65
-
-
Wang, J.1
Wang, W.2
Li, R.3
Li, Y.4
Tian, G.5
Goodman, L.6
Fan, W.7
Zhang, J.8
Li, J.9
Guo, Y.10
-
43
-
-
33644876210
-
DrugBank: a comprehensive resource for in silico drug discovery and exploration
-
Wishart DS, Knox C, Guo AC, Shrivastava S, Hassanali M, Stothard P, Chang Z, Woolsey J. 2006. DrugBank: a comprehensive resource for in silico drug discovery and exploration. Nucleic Acids Res 34:D668-D672.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Wishart, D.S.1
Knox, C.2
Guo, A.C.3
Shrivastava, S.4
Hassanali, M.5
Stothard, P.6
Chang, Z.7
Woolsey, J.8
|