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Ensembl 2002: accommodating comparative genomics.

M. Clamp, T. Andrews, D. Barker, P. Bevan, G. Cameron, Y. Chen, L. Clarke, T. Cox, J. Cuff, V. Curwen, T. Down, R. Durbin, E. Eyras, J. Gilbert, M. Hammond, T. Hubbard, A. Kasprzyk, D. Keefe, H. Lehväslaiho, V. Iyer, C. Melsopp, E. Mongin, R. Pettett, S. Potter, A. Rust, E. Schmidt, S. Searle, G. Slater, J. Smith, W. Spooner, A. Stabenau, J. Stalker, E. Stupka, A. Ureta-Vidal, I. Vastrik, and E. Birney. Nucleic Acids Research, 31 (1): 38-42 (2003)

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The Ensembl genome database project.T. Hubbard, D. Barker, E. Birney, G. Cameron, Y. Chen, L. Clarke, T. Cox, J. Cuff, V. Curwen, T. Down and 25 other author(s). Nucleic Acids Research, 30 (1): 38-41 (2002)HGBASE: a database of SNPs and other variations in and around human genes.A. Brookes, H. Lehväslaiho, M. Siegfried, J. Boehm, Y. Yuan, C. Sarkar, P. Bork, and J. Ortigao. Nucleic Acids Research, 28 (1): 356-360 (2000)Ensembl 2004.E. Birney, T. Andrews, P. Bevan, M. Cáccamo, G. Cameron, Y. Chen, L. Clarke, G. Coates, T. Cox, J. Cuff and 38 other author(s). Nucleic Acids Research, 32 (Database-Issue): 468-470 (2004)The DBCLS BioHackathon: standardization and interoperability for bioinformatics web services and workflows.T. Katayama, K. Arakawa, M. Nakao, K. Ono, K. Aoki-Kinoshita, Y. Yamamoto, A. Yamaguchi, S. Kawashima, H. Chun, J. Aerts and 47 other author(s). J. Biomedical Semantics, (2010)Human Sequence Variation and Mutation Databases.H. Lehväslaiho. Briefings in Bioinformatics, 1 (1): 161-166 (2000)Shape analysis of 3D nanoscale reconstructions of brain cell nuclear envelopes by implicit and explicit parametric representations.M. Agus, M. Castillo, J. Molina, E. Gobbetti, H. Lehväslaiho, A. Morales, P. Magistretti, M. Hadwiger, and C. Calì. Comput. Graph. X, (2019)MutRes and LsdbRes: A Bioinformatics Platform for Mutation Databases.P. Marín-García, and H. Lehväslaiho. Spanish Bioinformatics Conference, page 100. Technical University of Catalonia, Barcelona, (2004)Ensembl 2002: accommodating comparative genomics.M. Clamp, T. Andrews, D. Barker, P. Bevan, G. Cameron, Y. Chen, L. Clarke, T. Cox, J. Cuff, V. Curwen and 26 other author(s). Nucleic Acids Research, 31 (1): 38-42 (2003)HGVbase: a curated resource describing human DNA variation and phenotype relationships.D. Fredman, G. Munns, D. Rios, F. Sjöholm, M. Siegfried, B. Lenhard, H. Lehväslaiho, and A. Brookes. Nucleic Acids Research, 32 (Database-Issue): 516-519 (2004)HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources.D. Fredman, M. Siegfried, Y. Yuan, P. Bork, H. Lehväslaiho, and A. Brookes. Nucleic Acids Research, 30 (1): 387-391 (2002)

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Ensembl 2002: accommodating comparative genomics.

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Disambiguation of "Lehväslaiho, Heikki"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Ensembl 2002: accommodating comparative genomics.

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Ensembl 2002: accommodating comparative genomics.