-
1
-
-
80054746492
-
Exome sequencing as a tool for Mendelian disease gene discovery
-
Bamshad,M.J., Ng,S.B., Bigham,A.W., Tabor,H.K., Emond,M.J., Nickerson,D.A. and Shendure,J. (2011) Exome sequencing as a tool for Mendelian disease gene discovery. Nat. Rev. Genet., 12, 745-755.
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 745-755
-
-
Bamshad, M.J.1
Ng, S.B.2
Bigham, A.W.3
Tabor, H.K.4
Emond, M.J.5
Nickerson, D.A.6
Shendure, J.7
-
2
-
-
73349110071
-
Exome sequencing identifies the cause of a mendelian disorder
-
Ng,S.B., Buckingham,K.J., Lee,C., Bigham,A.W., Tabor,H.K., Dent,K.M., Huff,C.D., Shannon,P.T., Jabs,E.W., Nickerson,D.A. et al. (2010) Exome sequencing identifies the cause of a mendelian disorder. Nat. Genet., 42, 30-35.
-
(2010)
Nat. Genet.
, vol.42
, pp. 30-35
-
-
Ng, S.B.1
Buckingham, K.J.2
Lee, C.3
Bigham, A.W.4
Tabor, H.K.5
Dent, K.M.6
Huff, C.D.7
Shannon, P.T.8
Jabs, E.W.9
Nickerson, D.A.10
-
3
-
-
84875758730
-
Lessons from the cancer genome
-
Garraway,L.A. and Lander,E.S. (2013) Lessons from the cancer genome. Cell, 153, 17-37.
-
(2013)
Cell
, vol.153
, pp. 17-37
-
-
Garraway, L.A.1
Lander, E.S.2
-
4
-
-
84875490185
-
Cancer genome landscapes
-
Vogelstein,B., Papadopoulos,N., Velculescu,V.E., Zhou,S., Diaz,L.A. Jr and Kinzler,K.W. (2013) Cancer genome landscapes. Science, 339, 1546-1558.
-
(2013)
Science
, vol.339
, pp. 1546-1558
-
-
Vogelstein, B.1
Papadopoulos, N.2
Velculescu, V.E.3
Zhou, S.4
Diaz Jr., L.A.5
Kinzler, K.W.6
-
5
-
-
80051968181
-
Needles in stacks of needles: Finding disease-causal variants in a wealth of genomic data
-
Cooper,G.M. and Shendure,J. (2011) Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data. Nat. Rev. Genet., 12, 628-640.
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 628-640
-
-
Cooper, G.M.1
Shendure, J.2
-
6
-
-
84879411643
-
Sequencing studies in human genetics: Design and interpretation
-
Goldstein,D.B., Allen,A., Keebler,J., Margulies,E.H., Petrou,S., Petrovski,S. and Sunyaev,S. (2013) Sequencing studies in human genetics: design and interpretation. Nat. Rev. Genet., 14, 460-470.
-
(2013)
Nat. Rev. Genet.
, vol.14
, pp. 460-470
-
-
Goldstein, D.B.1
Allen, A.2
Keebler, J.3
Margulies, E.H.4
Petrou, S.5
Petrovski, S.6
Sunyaev, S.7
-
7
-
-
77956295988
-
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna,A., Hanna,M., Banks,E., Sivachenko,A., Cibulskis,K., Kernytsky,A., Garimella,K., Altshuler,D., Gabriel,S., Daly,M. et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res., 20, 1297-1303.
-
(2010)
Genome Res.
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
Kernytsky, A.6
Garimella, K.7
Altshuler, D.8
Gabriel, S.9
Daly, M.10
-
8
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo,M.A., Banks,E., Poplin,R., Garimella,K.V., Maguire,J.R., Hartl,C., Philippakis,A.A., del Angel,G., Rivas,M.A., Hanna,M. et al. (2011) A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet., 43, 491-498.
-
(2011)
Nat. Genet.
, vol.43
, pp. 491-498
-
-
Depristo, M.A.1
Banks, E.2
Poplin, R.3
Garimella, K.V.4
Maguire, J.R.5
Hartl, C.6
Philippakis, A.A.7
Del Angel, G.8
Rivas, M.A.9
Hanna, M.10
-
9
-
-
68549104404
-
The Sequence Alignment/Map format and SAMtools
-
Li,H., Handsaker,B., Wysoker,A., Fennell,T., Ruan,J., Homer,N., Marth,G., Abecasis,G. and Durbin,R. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics, 25, 2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
Homer, N.6
Marth, G.7
Abecasis, G.8
Durbin, R.9
-
10
-
-
84864486576
-
VARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing
-
Medina,I., De Maria,A., Bleda,M., Salavert,F., Alonso,R., Gonzalez,C.Y. and Dopazo,J. (2012) VARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing. Nucleic Acids Res., 40, W54-W58.
-
(2012)
Nucleic Acids Res.
, vol.40
-
-
Medina, I.1
De Maria, A.2
Bleda, M.3
Salavert, F.4
Alonso, R.5
Gonzalez, C.Y.6
Dopazo, J.7
-
11
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
-
Wang,K., Li,M. and 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
-
12
-
-
84874609313
-
Rare variant detection using family-based sequencing analysis
-
Peng,G., Fan,Y., Palculict,T.B., Shen,P., Ruteshouser,E.C., Chi,A.K., Davis,R.W., Huff,V., Scharfe,C. and Wang,W. (2013) Rare variant detection using family-based sequencing analysis. Proc. Natl. Acad. Sci. U.S.A., 110, 3985-3990.
-
(2013)
Proc. Natl. Acad. Sci. U.S.A.
, vol.110
, pp. 3985-3990
-
-
Peng, G.1
Fan, Y.2
Palculict, T.B.3
Shen, P.4
Ruteshouser, E.C.5
Chi, A.K.6
Davis, R.W.7
Huff, V.8
Scharfe, C.9
Wang, W.10
-
13
-
-
84868138663
-
A likelihood-based framework for variant calling and de novo mutation detection in families
-
Li,B., Chen,W., Zhan,X., Busonero,F., Sanna,S., Sidore,C., Cucca,F., Kang,H.M. and Abecasis,G.R. (2012) A likelihood-based framework for variant calling and de novo mutation detection in families. PLoS Genet., 8, e1002944.
-
(2012)
PLoS Genet.
, vol.8
-
-
Li, B.1
Chen, W.2
Zhan, X.3
Busonero, F.4
Sanna, S.5
Sidore, C.6
Cucca, F.7
Kang, H.M.8
Abecasis, G.R.9
-
14
-
-
84863229597
-
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
-
Koboldt,D.C., Zhang,Q., Larson,D.E., Shen,D., McLellan,M.D., Lin,L., Miller,C.A., Mardis,E.R., Ding,L. and Wilson,R.K. (2012) VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res., 22, 568-576.
-
(2012)
Genome Res.
, vol.22
, pp. 568-576
-
-
Koboldt, D.C.1
Zhang, Q.2
Larson, D.E.3
Shen, D.4
McLellan, M.D.5
Lin, L.6
Miller, C.A.7
Mardis, E.R.8
Ding, L.9
Wilson, R.K.10
-
15
-
-
84860147579
-
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases
-
Li,M.X., Gui,H.S., Kwan,J.S., Bao,S.Y. and Sham,P.C. (2012) A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases. Nucleic Acids Res., 40, e53.
-
(2012)
Nucleic Acids Res.
, vol.40
-
-
Li, M.X.1
Gui, H.S.2
Kwan, J.S.3
Bao, S.Y.4
Sham, P.C.5
-
16
-
-
79960405019
-
The variant call format and VCFtools
-
Danecek,P., Auton,A., Abecasis,G., Albers,C.A., Banks,E., DePristo,M.A., Handsaker,R.E., Lunter,G., Marth,G.T., Sherry,S.T. et al. (2011) The variant call format and VCFtools. Bioinformatics, 27, 2156-2158.
-
(2011)
Bioinformatics
, vol.27
, pp. 2156-2158
-
-
Danecek, P.1
Auton, A.2
Abecasis, G.3
Albers, C.A.4
Banks, E.5
Depristo, M.A.6
Handsaker, R.E.7
Lunter, G.8
Marth, G.T.9
Sherry, S.T.10
-
17
-
-
84864438093
-
CellBase, a comprehensive collection of RESTful web services for retrieving relevant biological information from heterogeneous sources
-
Bleda,M., Tarraga,J., de Maria,A., Salavert,F., Garcia-Alonso,L., Celma,M., Martin,A., Dopazo,J. and Medina,I. (2012) CellBase, a comprehensive collection of RESTful web services for retrieving relevant biological information from heterogeneous sources. Nucleic Acids Res., 40, W609-W614.
-
(2012)
Nucleic Acids Res.
, vol.40
-
-
Bleda, M.1
Tarraga, J.2
De Maria, A.3
Salavert, F.4
Garcia-Alonso, L.5
Celma, M.6
Martin, A.7
Dopazo, J.8
Medina, I.9
-
18
-
-
0035173378
-
DbSNP: The NCBI database of genetic variation
-
Sherry,S.T., Ward,M.H., Kholodov,M., Baker,J., Phan,L., Smigielski,E.M. and 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
-
19
-
-
0036713510
-
Human non-synonymous SNPs: Server and survey
-
Ramensky,V., Bork,P. and Sunyaev,S. (2002) Human non-synonymous SNPs: server and survey. Nucleic Acids Res., 30, 3894-3900.
-
(2002)
Nucleic Acids Res.
, vol.30
, pp. 3894-3900
-
-
Ramensky, V.1
Bork, P.2
Sunyaev, S.3
-
20
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
Kumar,P., Henikoff,S. and Ng,P.C. (2009) Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat. Protoc., 4, 1073-1081.
-
(2009)
Nat. Protoc.
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
21
-
-
84891768365
-
Ensembl 2014
-
Flicek,P., Amode,M.R., Barrell,D., Beal,K., Billis,K., Brent,S., Carvalho-Silva,D., Clapham,P., Coates,G., Fitzgerald,S. et al. (2014) Ensembl 2014. Nucleic Acids Res., 42, D749-D755.
-
(2014)
Nucleic Acids Res.
, vol.42
-
-
Flicek, P.1
Amode, M.R.2
Barrell, D.3
Beal, K.4
Billis, K.5
Brent, S.6
Carvalho-Silva, D.7
Clapham, P.8
Coates, G.9
Fitzgerald, S.10
-
22
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
Durbin,R.M., Abecasis,G.R., Altshuler,D.L., Auton,A., Brooks,L.D., Gibbs,R.A., Hurles,M.E. and McVean,G.A. (2010) A map of human genome variation from population-scale sequencing. Nature, 467, 1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Durbin, R.M.1
Abecasis, G.R.2
Altshuler, D.L.3
Auton, A.4
Brooks, L.D.5
Gibbs, R.A.6
Hurles, M.E.7
McVean, G.A.8
-
23
-
-
84872143942
-
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
-
Fu,W., O'Connor,T.D., Jun,G., Kang,H.M., Abecasis,G., Leal,S.M., Gabriel,S., Rieder,M.J., Altshuler,D., Shendure,J. et al. (2013) Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants. Nature, 493, 216-220.
-
(2013)
Nature
, vol.493
, pp. 216-220
-
-
Fu, W.1
O'connor, T.D.2
Jun, G.3
Kang, H.M.4
Abecasis, G.5
Leal, S.M.6
Gabriel, S.7
Rieder, M.J.8
Altshuler, D.9
Shendure, J.10
-
24
-
-
84868343901
-
The Human Gene Mutation Database (HGMD) and its exploitation in the fields of personalized genomics and molecular evolution
-
Chapter 1, Unit1 13
-
Stenson,P.D., Ball,E.V., Mort,M., Phillips,A.D., Shaw,K. and Cooper,D.N. (2012) The Human Gene Mutation Database (HGMD) and its exploitation in the fields of personalized genomics and molecular evolution. Curr. Protoc. Bioinformatics, Chapter 1, Unit1 13.
-
(2012)
Curr. Protoc. Bioinformatics
, vol.1
-
-
Stenson, P.D.1
Ball, E.V.2
Mort, M.3
Phillips, A.D.4
Shaw, K.5
Cooper, D.N.6
-
25
-
-
84891809093
-
ClinVar: Public archive of relationships among sequence variation and human phenotype
-
Landrum,M.J., Lee,J.M., Riley,G.R., Jang,W., Rubinstein,W.S., Church,D.M. and Maglott,D.R. (2014) ClinVar: public archive of relationships among sequence variation and human phenotype. Nucleic Acids Res., 42, D980-D985.
-
(2014)
Nucleic Acids Res.
, vol.42
-
-
Landrum, M.J.1
Lee, J.M.2
Riley, G.R.3
Jang, W.4
Rubinstein, W.S.5
Church, D.M.6
Maglott, D.R.7
-
26
-
-
84891783174
-
Activities at the Universal Protein Resource (UniProt)
-
The Uniprot Consortium
-
The Uniprot Consortium. (2014) Activities at the Universal Protein Resource (UniProt). Nucleic Acids Res., 42, D191-D198.
-
(2014)
Nucleic Acids Res.
, vol.42
-
-
-
27
-
-
84883592733
-
Genome Maps, a new generation genome browser
-
Medina,I., Salavert,F., Sanchez,R., de Maria,A., Alonso,R., Escobar,P., Bleda,M. and Dopazo,J. (2013) Genome Maps, a new generation genome browser. Nucleic Acids Res., 41, W41-W46.
-
(2013)
Nucleic Acids Res.
, vol.41
-
-
Medina, I.1
Salavert, F.2
Sanchez, R.3
De Maria, A.4
Alonso, R.5
Escobar, P.6
Bleda, M.7
Dopazo, J.8
-
28
-
-
84896137184
-
Two novel mutations in the bckdk gene (branched-chain keto-acid dehydrogenase kinase) are responsible of a neurobehavioral deficit in two pediatric unrelated patients
-
Garcia-Cazorla,A., Oyarzabal,A., Fort,J., Robles,C., Castejon,E., Ruiz-Sala,P., Bodoy,S., Merinero,B., Lopez-Sala,A., Dopazo,J. et al. (2014) Two Novel Mutations in the BCKDK Gene (Branched-Chain Keto-Acid Dehydrogenase Kinase) are Responsible of a Neurobehavioral Deficit in two Pediatric Unrelated Patients. Hum. Mutat.
-
(2014)
Hum. Mutat
-
-
Garcia-Cazorla, A.1
Oyarzabal, A.2
Fort, J.3
Robles, C.4
Castejon, E.5
Ruiz-Sala, P.6
Bodoy, S.7
Merinero, B.8
Lopez-Sala, A.9
Dopazo, J.10
-
29
-
-
84895543557
-
Combined genetic and high-throughput strategies for molecular diagnosis of inherited retinal dystrophies
-
de Castro-Miro,M., Pomares,E., Lores-Motta,L., Tonda,R., Dopazo,J., Marfany,G. and Gonzalez-Duarte,R. (2014) Combined genetic and high-throughput strategies for molecular diagnosis of inherited retinal dystrophies. PLoS ONE, 9, e88410.
-
(2014)
PLoS ONE
, vol.9
-
-
De Castro-Miro, M.1
Pomares, E.2
Lores-Motta, L.3
Tonda, R.4
Dopazo, J.5
Marfany, G.6
Gonzalez-Duarte, R.7
-
30
-
-
84887266834
-
Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa
-
Mendez-Vidal,C., Gonzalez-Del Pozo,M., Vela-Boza,A., Santoyo-Lopez,J., Lopez-Domingo,F.J., Vazquez-Marouschek,C., Dopazo,J., Borrego,S. and Antinolo,G. (2013) Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa. Mol. Vis., 19, 2187-2195.
-
(2013)
Mol. Vis.
, vol.19
, pp. 2187-2195
-
-
Mendez-Vidal, C.1
Gonzalez-Del Pozo, M.2
Vela-Boza, A.3
Santoyo-Lopez, J.4
Lopez-Domingo, F.J.5
Vazquez-Marouschek, C.6
Dopazo, J.7
Borrego, S.8
Antinolo, G.9
-
31
-
-
82555175936
-
Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencing
-
Gonzalez-del Pozo,M., Borrego,S., Barragan,I., Pieras,J.I., Santoyo,J., Matamala,N., Naranjo,B., Dopazo,J. and Antinolo,G. (2011) Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencing. PLoS ONE, 6, e27894.
-
(2011)
PLoS ONE
, vol.6
-
-
Gonzalez-Del Pozo, M.1
Borrego, S.2
Barragan, I.3
Pieras, J.I.4
Santoyo, J.5
Matamala, N.6
Naranjo, B.7
Dopazo, J.8
Antinolo, G.9
-
32
-
-
78049441932
-
Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa
-
Barragan,I., Borrego,S., Pieras,J.I., Gonzalez-del Pozo,M., Santoyo,J., Ayuso,C., Baiget,M., Millan,J.M., Mena,M., Abd El-Aziz,M.M. et al. (2010) Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa. Hum. Mutat., 31, E1772-E1800.
-
(2010)
Hum. Mutat.
, vol.31
-
-
Barragan, I.1
Borrego, S.2
Pieras, J.I.3
Gonzalez-Del Pozo, M.4
Santoyo, J.5
Ayuso, C.6
Baiget, M.7
Millan, J.M.8
Mena, M.9
Abd El-Aziz, M.M.10
-
33
-
-
84882814856
-
Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria
-
Tort,F., Garcia-Silva,M.T., Ferrer-Cortes,X., Navarro-Sastre,A., Garcia-Villoria,J., Coll,M.J., Vidal,E., Jimenez-Almazan,J., Dopazo,J., Briones,P. et al. (2013) Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria. Mol. Genet. Metab., 110, 73-77.
-
(2013)
Mol. Genet. Metab.
, vol.110
, pp. 73-77
-
-
Tort, F.1
Garcia-Silva, M.T.2
Ferrer-Cortes, X.3
Navarro-Sastre, A.4
Garcia-Villoria, J.5
Coll, M.J.6
Vidal, E.7
Jimenez-Almazan, J.8
Dopazo, J.9
Briones, P.10
-
34
-
-
84893681804
-
Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster
-
Santoni,F.A., Makrythanasis,P., Nikolaev,S., Guipponi,M., Robyr,D., Bottani,A. and Antonarakis,S.E. (2014) Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster. Genome Res., 24, 349-355.
-
(2014)
Genome Res.
, vol.24
, pp. 349-355
-
-
Santoni, F.A.1
Makrythanasis, P.2
Nikolaev, S.3
Guipponi, M.4
Robyr, D.5
Bottani, A.6
Antonarakis, S.E.7
-
35
-
-
84863556835
-
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
-
Tennessen,J.A., Bigham,A.W., O'Connor,T.D., Fu,W., Kenny,E.E., Gravel,S., McGee,S., Do,R., Liu,X., Jun,G. et al. (2012) Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science, 337, 64-69.
-
(2012)
Science
, vol.337
, pp. 64-69
-
-
Tennessen, J.A.1
Bigham, A.W.2
O'connor, T.D.3
Fu, W.4
Kenny, E.E.5
Gravel, S.6
McGee, S.7
Do, R.8
Liu, X.9
Jun, G.10
-
36
-
-
67849101190
-
SNOW, a web-based tool for the statistical analysis of protein-protein interaction networks
-
Minguez,P., Gotz,S., Montaner,D., Al-Shahrour,F. and Dopazo,J. (2009) SNOW, a web-based tool for the statistical analysis of protein-protein interaction networks. Nucleic Acids Res., 37, W109-W114.
-
(2009)
Nucleic Acids Res.
, vol.37
-
-
Minguez, P.1
Gotz, S.2
Montaner, D.3
Al-Shahrour, F.4
Dopazo, J.5
-
37
-
-
76249105279
-
Genome-wide prioritization of disease genes and identification of disease-disease associations from an integrated human functional linkage network
-
Linghu,B., Snitkin,E.S., Hu,Z., Xia,Y. and Delisi,C. (2009) Genome-wide prioritization of disease genes and identification of disease-disease associations from an integrated human functional linkage network. Genome Biol., 10, R91.
-
(2009)
Genome Biol.
, vol.10
-
-
Linghu, B.1
Snitkin, E.S.2
Hu, Z.3
Xia, Y.4
Delisi, C.5
-
38
-
-
84863987708
-
Computational tools for prioritizing candidate genes: Boosting disease gene discovery
-
Moreau,Y. and Tranchevent,L.C. (2012) Computational tools for prioritizing candidate genes: boosting disease gene discovery. Nat. Rev. Genet., 13, 523-536.
-
(2012)
Nat. Rev. Genet.
, vol.13
, pp. 523-536
-
-
Moreau, Y.1
Tranchevent, L.C.2
-
39
-
-
77954339096
-
Babelomics: An integrative platform for the analysis of transcriptomics, proteomics and genomic data with advanced functional profiling
-
Medina,I., Carbonell,J., Pulido,L., Madeira,S.C., Goetz,S., Conesa,A., Tarraga,J., Pascual-Montano,A., Nogales-Cadenas,R., Santoyo,J. et al. (2010) Babelomics: an integrative platform for the analysis of transcriptomics, proteomics and genomic data with advanced functional profiling. Nucleic Acids Res., 38, W210-W213.
-
(2010)
Nucleic Acids Res.
, vol.38
-
-
Medina, I.1
Carbonell, J.2
Pulido, L.3
Madeira, S.C.4
Goetz, S.5
Conesa, A.6
Tarraga, J.7
Pascual-Montano, A.8
Nogales-Cadenas, R.9
Santoyo, J.10
|