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Eric Banks

Showing results (1-10 of 54) with videos related to

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Genome Biology|September 20, 2008
NetGrep: fast network schema searches in interactomesEric Banks, Elena Nabieva, Ryan Peterson, et al.
Bioinformatics (Oxford, England)|December 13, 2019
Lean and deep models for more accurate filtering of SNP and INDEL variant callsSam Friedman, Laura Gauthier, Yossi Farjoun, et al.
Plos Computational Biology|October 25, 2008
Organization of physical interactomes as uncovered by network schemasEric Banks, Elena Nabieva, Bernard Chazelle, et al.
Acta Crystallographica. Section C, Crystal Structure Communications|April 12, 2003
N-fluoropyridinium trifluoromethanesulfonate and 1-fluoro-2,4,6-trimethoxy-1,3,5-triazinium hexafluoroantimonate: the first experimental determination of the F-N+ bond length involving sp2 nitrogenR Eric Banks, Mohamed K Besheesh, Robin G Pritchard
Bioinformatics (Oxford, England)|August 2, 2011
ContEst: estimating cross-contamination of human samples in next-generation sequencing dataKristian Cibulskis, Aaron McKenna, Tim Fennell, et al.
Genome Biology|September 19, 2015
Tools and best practices for data processing in allelic expression analysisStephane E Castel, Ami Levy-Moonshine, Pejman Mohammadi, et al.
Fertility and Sterility|September 19, 2012
Reducing multiples: a mathematical formula that accurately predicts rates of singletons, twins, and higher-order multiples in women undergoing in vitro fertilizationZev Williams, Eric Banks, Mario Bkassiny, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Blended Length Genome Sequencing (blend-seq): Combining Short Reads with Low-Coverage Long Reads to Maximize Variant DiscoveryRicky Magner, Fabio Cunial, Sumit Basu, et al.
Plos Computational Biology|July 19, 2012
Efficiency and power as a function of sequence coverage, SNP array density, and imputationJason Flannick, Joshua M Korn, Pierre Fontanillas, et al.
Communications Biology|December 9, 2020
A validated lineage-derived somatic truth data set enables benchmarking in cancer genome analysisMegan Shand, Jose Soto, Lee Lichtenstein, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Genome Biology|September 20, 2008
NetGrep: fast network schema searches in interactomesEric Banks, Elena Nabieva, Ryan Peterson, et al.
Bioinformatics (Oxford, England)|December 13, 2019
Lean and deep models for more accurate filtering of SNP and INDEL variant callsSam Friedman, Laura Gauthier, Yossi Farjoun, et al.
Plos Computational Biology|October 25, 2008
Organization of physical interactomes as uncovered by network schemasEric Banks, Elena Nabieva, Bernard Chazelle, et al.
Acta Crystallographica. Section C, Crystal Structure Communications|April 12, 2003
N-fluoropyridinium trifluoromethanesulfonate and 1-fluoro-2,4,6-trimethoxy-1,3,5-triazinium hexafluoroantimonate: the first experimental determination of the F-N+ bond length involving sp2 nitrogenR Eric Banks, Mohamed K Besheesh, Robin G Pritchard
Bioinformatics (Oxford, England)|August 2, 2011
ContEst: estimating cross-contamination of human samples in next-generation sequencing dataKristian Cibulskis, Aaron McKenna, Tim Fennell, et al.
Genome Biology|September 19, 2015
Tools and best practices for data processing in allelic expression analysisStephane E Castel, Ami Levy-Moonshine, Pejman Mohammadi, et al.
Fertility and Sterility|September 19, 2012
Reducing multiples: a mathematical formula that accurately predicts rates of singletons, twins, and higher-order multiples in women undergoing in vitro fertilizationZev Williams, Eric Banks, Mario Bkassiny, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Blended Length Genome Sequencing (blend-seq): Combining Short Reads with Low-Coverage Long Reads to Maximize Variant DiscoveryRicky Magner, Fabio Cunial, Sumit Basu, et al.
Plos Computational Biology|July 19, 2012
Efficiency and power as a function of sequence coverage, SNP array density, and imputationJason Flannick, Joshua M Korn, Pierre Fontanillas, et al.
Communications Biology|December 9, 2020
A validated lineage-derived somatic truth data set enables benchmarking in cancer genome analysisMegan Shand, Jose Soto, Lee Lichtenstein, et al.
Pageof 6