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Andrew Carroll

Showing results (81-90 of 119) with videos related to

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Science (New York, N.Y.)|December 16, 2021
Pangenomics enables genotyping of known structural variants in 5202 diverse genomesJouni Sirén, Jean Monlong, Xian Chang, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 7, 2009
Improved early event-free survival with imatinib in Philadelphia chromosome-positive acute lymphoblastic leukemia: a children's oncology group studyKirk R Schultz, W Paul Bowman, Alexander Aledo, et al.
Plos Computational Biology|June 20, 2020
A crowdsourced set of curated structural variants for the human genomeLesley M Chapman, Noah Spies, Patrick Pai, et al.
Nature Communications|September 23, 2020
A diploid assembly-based benchmark for variants in the major histocompatibility complexChen-Shan Chin, Justin Wagner, Qiandong Zeng, et al.
Nature Genetics|February 8, 2011
Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemiaJun J Yang, Cheng Cheng, Meenakshi Devidas, et al.
Nature Biotechnology|August 14, 2019
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genomeAaron M Wenger, Paul Peluso, William J Rowell, 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.
Biorxiv : the Preprint Server for Biology|September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologiesJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
American Journal of Human Genetics|April 28, 2026
Sensitivity of HiFi long-read genome sequencing for difficult-to-detect pathogenic variants when applied to real-world clinical laboratory samplesJoseph M Devaney, Jessica X Chong, Patricia C Lopes, et al.
Nature Biotechnology|March 29, 2022
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencingSneha D Goenka, John E Gorzynski, Kishwar Shafin, et al.
Pageof 12

Showing results (81-90 of 119) with videos related to

Sort By:
Pageof 12
Science (New York, N.Y.)|December 16, 2021
Pangenomics enables genotyping of known structural variants in 5202 diverse genomesJouni Sirén, Jean Monlong, Xian Chang, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 7, 2009
Improved early event-free survival with imatinib in Philadelphia chromosome-positive acute lymphoblastic leukemia: a children's oncology group studyKirk R Schultz, W Paul Bowman, Alexander Aledo, et al.
Plos Computational Biology|June 20, 2020
A crowdsourced set of curated structural variants for the human genomeLesley M Chapman, Noah Spies, Patrick Pai, et al.
Nature Communications|September 23, 2020
A diploid assembly-based benchmark for variants in the major histocompatibility complexChen-Shan Chin, Justin Wagner, Qiandong Zeng, et al.
Nature Genetics|February 8, 2011
Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemiaJun J Yang, Cheng Cheng, Meenakshi Devidas, et al.
Nature Biotechnology|August 14, 2019
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genomeAaron M Wenger, Paul Peluso, William J Rowell, 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.
Biorxiv : the Preprint Server for Biology|September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologiesJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
American Journal of Human Genetics|April 28, 2026
Sensitivity of HiFi long-read genome sequencing for difficult-to-detect pathogenic variants when applied to real-world clinical laboratory samplesJoseph M Devaney, Jessica X Chong, Patricia C Lopes, et al.
Nature Biotechnology|March 29, 2022
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencingSneha D Goenka, John E Gorzynski, Kishwar Shafin, et al.
Pageof 12