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Jennifer McDaniel

Showing results (11-20 of 23) with videos related to

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Nature Biotechnology|April 3, 2019
An open resource for accurately benchmarking small variant and reference callsJustin M Zook, Jennifer McDaniel, Nathan D Olson, et al.
Nature Communications|January 8, 2025
Small variant benchmark from a complete assembly of X and Y chromosomesJustin Wagner, Nathan D Olson, Jennifer McDaniel, et al.
Science (New York, N.Y.)|March 31, 2022
A complete reference genome improves analysis of human genetic variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Science Translational Medicine|August 15, 2014
Intratumoral injection of Clostridium novyi-NT spores induces antitumor responsesNicholas J Roberts, Linping Zhang, Filip Janku, et al.
Nature Biotechnology|February 8, 2022
Curated variation benchmarks for challenging medically relevant autosomal genesJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Biomolecular Detection and Quantification|June 24, 2016
An international comparability study on quantification of mRNA gene expression ratios: CCQM-P103.1Alison S Devonshire, Rebecca Sanders, Alexandra S Whale, et al.
Scientific Data|June 9, 2016
Extensive sequencing of seven human genomes to characterize benchmark reference materialsJustin M Zook, David Catoe, Jennifer McDaniel, et al.
Cell Genomics|June 20, 2022
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regionsNathan D Olson, Justin Wagner, Jennifer McDaniel, et al.
Nature|October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomesErich D Jarvis, Giulio Formenti, Arang Rhie, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
A complete human pancreatic cancer genomeJustin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Nature Biotechnology|April 3, 2019
An open resource for accurately benchmarking small variant and reference callsJustin M Zook, Jennifer McDaniel, Nathan D Olson, et al.
Nature Communications|January 8, 2025
Small variant benchmark from a complete assembly of X and Y chromosomesJustin Wagner, Nathan D Olson, Jennifer McDaniel, et al.
Science (New York, N.Y.)|March 31, 2022
A complete reference genome improves analysis of human genetic variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Science Translational Medicine|August 15, 2014
Intratumoral injection of Clostridium novyi-NT spores induces antitumor responsesNicholas J Roberts, Linping Zhang, Filip Janku, et al.
Nature Biotechnology|February 8, 2022
Curated variation benchmarks for challenging medically relevant autosomal genesJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Biomolecular Detection and Quantification|June 24, 2016
An international comparability study on quantification of mRNA gene expression ratios: CCQM-P103.1Alison S Devonshire, Rebecca Sanders, Alexandra S Whale, et al.
Scientific Data|June 9, 2016
Extensive sequencing of seven human genomes to characterize benchmark reference materialsJustin M Zook, David Catoe, Jennifer McDaniel, et al.
Cell Genomics|June 20, 2022
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regionsNathan D Olson, Justin Wagner, Jennifer McDaniel, et al.
Nature|October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomesErich D Jarvis, Giulio Formenti, Arang Rhie, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
A complete human pancreatic cancer genomeJustin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Pageof 3