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Marc Salit

Showing results (21-30 of 51) with videos related to

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Nature Reviews. Genetics|April 14, 2023
Variant calling and benchmarking in an era of complete human genome sequencesNathan D Olson, Justin Wagner, Nathan Dwarshuis, et al.
Genome Research|August 6, 2011
Synthetic spike-in standards for RNA-seq experimentsLichun Jiang, Felix Schlesinger, Carrie A Davis, et al.
BMC Biotechnology|March 21, 2018
Cell-based reference samples designed with specific differences in microRNA biomarkersP Scott Pine, Steven P Lund, Sanford A Stass, et al.
Nucleic Acids Research|March 24, 2017
Measurements of translation initiation from all 64 codons in E. coliAriel Hecht, Jeff Glasgow, Paul R Jaschke, et al.
Genome Medicine|March 3, 2016
Medical implications of technical accuracy in genome sequencingRachel L Goldfeder, James R Priest, Justin M Zook, et al.
Nature|March 3, 2006
Top-down standards will not serve systems biologyJohn Quackenbush, Christian Stoeckert, Catherine Ball, et al.
Nature Methods|July 18, 2017
Genome-wide reconstruction of complex structural variants using read cloudsNoah Spies, Ziming Weng, Alex Bishara, et al.
Nature|June 21, 2023
Single-cell quantification of ribosome occupancy in early mouse developmentHakan Ozadam, Tori Tonn, Crystal M Han, et al.
BMC Genomics|January 17, 2016
svclassify: a method to establish benchmark structural variant callsHemang Parikh, Marghoob Mohiyuddin, Hugo Y K Lam, et al.
The Journal of Molecular Diagnostics : JMD|January 6, 2019
A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic TestingStephen E Lincoln, Rebecca Truty, Chiao-Feng Lin, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Nature Reviews. Genetics|April 14, 2023
Variant calling and benchmarking in an era of complete human genome sequencesNathan D Olson, Justin Wagner, Nathan Dwarshuis, et al.
Genome Research|August 6, 2011
Synthetic spike-in standards for RNA-seq experimentsLichun Jiang, Felix Schlesinger, Carrie A Davis, et al.
BMC Biotechnology|March 21, 2018
Cell-based reference samples designed with specific differences in microRNA biomarkersP Scott Pine, Steven P Lund, Sanford A Stass, et al.
Nucleic Acids Research|March 24, 2017
Measurements of translation initiation from all 64 codons in E. coliAriel Hecht, Jeff Glasgow, Paul R Jaschke, et al.
Genome Medicine|March 3, 2016
Medical implications of technical accuracy in genome sequencingRachel L Goldfeder, James R Priest, Justin M Zook, et al.
Nature|March 3, 2006
Top-down standards will not serve systems biologyJohn Quackenbush, Christian Stoeckert, Catherine Ball, et al.
Nature Methods|July 18, 2017
Genome-wide reconstruction of complex structural variants using read cloudsNoah Spies, Ziming Weng, Alex Bishara, et al.
Nature|June 21, 2023
Single-cell quantification of ribosome occupancy in early mouse developmentHakan Ozadam, Tori Tonn, Crystal M Han, et al.
BMC Genomics|January 17, 2016
svclassify: a method to establish benchmark structural variant callsHemang Parikh, Marghoob Mohiyuddin, Hugo Y K Lam, et al.
The Journal of Molecular Diagnostics : JMD|January 6, 2019
A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic TestingStephen E Lincoln, Rebecca Truty, Chiao-Feng Lin, et al.
Pageof 6