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Steven E Brenner

Showing results (41-50 of 166) with videos related to

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Biorxiv : the Preprint Server for Biology|July 9, 2024
Variant Impact Predictor database (VIPdb), version 2: Trends from 25 years of genetic variant impact predictorsYu-Jen Lin, Arul S Menon, Zhiqiang Hu, et al.
Genome Medicine|July 13, 2023
ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burdenAndrew G Sharo, Yangyun Zou, Aashish N Adhikari, et al.
Genome Research|June 3, 2004
WebLogo: a sequence logo generatorGavin E Crooks, Gary Hon, John-Marc Chandonia, et al.
Journal of Structural Biology|January 27, 2009
A method for the alignment of heterogeneous macromolecules from electron microscopyMaxim Shatsky, Richard J Hall, Steven E Brenner, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 4, 2013
Personalized medicine: from genotypes and molecular phenotypes towards therapy- session introductionJennifer Listgarten, Oliver Stegle, Quaid Morris, et al.
Genome Research|July 3, 2014
Comparison of D. melanogaster and C. elegans developmental stages, tissues, and cells by modENCODE RNA-seq dataJingyi Jessica Li, Haiyan Huang, Peter J Bickel, et al.
Human Genomics|August 28, 2024
Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictorsYu-Jen Lin, Arul S Menon, Zhiqiang Hu, et al.
Plos Computational Biology|November 9, 2018
Putting benchmarks in their rightful place: The heart of computational biologyBjoern Peters, Steven E Brenner, Edwin Wang, et al.
Genome Research|July 26, 2011
Genome-scale phylogenetic function annotation of large and diverse protein familiesBarbara E Engelhardt, Michael I Jordan, John R Srouji, et al.
Proteins|November 25, 2004
A generalized affine gap model significantly improves protein sequence alignment accuracyMarcus A Zachariah, Gavin E Crooks, Stephen R Holbrook, et al.
Pageof 17

Showing results (41-50 of 166) with videos related to

Sort By:
Pageof 17
Biorxiv : the Preprint Server for Biology|July 9, 2024
Variant Impact Predictor database (VIPdb), version 2: Trends from 25 years of genetic variant impact predictorsYu-Jen Lin, Arul S Menon, Zhiqiang Hu, et al.
Genome Medicine|July 13, 2023
ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burdenAndrew G Sharo, Yangyun Zou, Aashish N Adhikari, et al.
Genome Research|June 3, 2004
WebLogo: a sequence logo generatorGavin E Crooks, Gary Hon, John-Marc Chandonia, et al.
Journal of Structural Biology|January 27, 2009
A method for the alignment of heterogeneous macromolecules from electron microscopyMaxim Shatsky, Richard J Hall, Steven E Brenner, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 4, 2013
Personalized medicine: from genotypes and molecular phenotypes towards therapy- session introductionJennifer Listgarten, Oliver Stegle, Quaid Morris, et al.
Genome Research|July 3, 2014
Comparison of D. melanogaster and C. elegans developmental stages, tissues, and cells by modENCODE RNA-seq dataJingyi Jessica Li, Haiyan Huang, Peter J Bickel, et al.
Human Genomics|August 28, 2024
Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictorsYu-Jen Lin, Arul S Menon, Zhiqiang Hu, et al.
Plos Computational Biology|November 9, 2018
Putting benchmarks in their rightful place: The heart of computational biologyBjoern Peters, Steven E Brenner, Edwin Wang, et al.
Genome Research|July 26, 2011
Genome-scale phylogenetic function annotation of large and diverse protein familiesBarbara E Engelhardt, Michael I Jordan, John R Srouji, et al.
Proteins|November 25, 2004
A generalized affine gap model significantly improves protein sequence alignment accuracyMarcus A Zachariah, Gavin E Crooks, Stephen R Holbrook, et al.
Pageof 17