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Nature Biotechnology
|
April 3, 2019
An open resource for accurately benchmarking small variant and reference calls
Justin 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 chromosomes
Justin 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 variation
Sergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Science Translational Medicine
|
August 15, 2014
Intratumoral injection of Clostridium novyi-NT spores induces antitumor responses
Nicholas J Roberts, Linping Zhang, Filip Janku, et al.
Nature Biotechnology
|
February 8, 2022
Curated variation benchmarks for challenging medically relevant autosomal genes
Justin 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-P103.1
Alison S Devonshire, Rebecca Sanders, Alexandra S Whale, et al.
Scientific Data
|
June 9, 2016
Extensive sequencing of seven human genomes to characterize benchmark reference materials
Justin 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 regions
Nathan D Olson, Justin Wagner, Jennifer McDaniel, et al.
Nature
|
October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomes
Erich D Jarvis, Giulio Formenti, Arang Rhie, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
A complete human pancreatic cancer genome
Justin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Nature Biotechnology
|
April 3, 2019
An open resource for accurately benchmarking small variant and reference calls
Justin 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 chromosomes
Justin 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 variation
Sergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Science Translational Medicine
|
August 15, 2014
Intratumoral injection of Clostridium novyi-NT spores induces antitumor responses
Nicholas J Roberts, Linping Zhang, Filip Janku, et al.
Nature Biotechnology
|
February 8, 2022
Curated variation benchmarks for challenging medically relevant autosomal genes
Justin 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-P103.1
Alison S Devonshire, Rebecca Sanders, Alexandra S Whale, et al.
Scientific Data
|
June 9, 2016
Extensive sequencing of seven human genomes to characterize benchmark reference materials
Justin 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 regions
Nathan D Olson, Justin Wagner, Jennifer McDaniel, et al.
Nature
|
October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomes
Erich D Jarvis, Giulio Formenti, Arang Rhie, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
A complete human pancreatic cancer genome
Justin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Page
of 3