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Genome Research|November 10, 2017
Comparative genome analysis of programmed DNA elimination in nematodesJianbin Wang, Shenghan Gao, Yulia Mostovoy, et al.
Nature Methods|May 10, 2016
A hybrid approach for de novo human genome sequence assembly and phasingYulia Mostovoy, Michal Levy-Sakin, Jessica Lam, et al.
Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
American Journal of Human Genetics|November 9, 2024
Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assemblyYulia Mostovoy, Philip M Boone, Yongqing Huang, et al.
Nature Communications|March 6, 2019
Genome maps across 26 human populations reveal population-specific patterns of structural variationMichal Levy-Sakin, Steven Pastor, Yulia Mostovoy, et al.
Nature Ecology & Evolution|July 31, 2019
Genome of the Komodo dragon reveals adaptations in the cardiovascular and chemosensory systems of monitor lizardsAbigail L Lind, Yvonne Y Y Lai, Yulia Mostovoy, et al.
Genetics|October 30, 2015
Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel ArraysAngel C Y Mak, Yvonne Y Y Lai, Ernest T Lam, et al.
Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Population-scale Long-read Sequencing in the <i>All of Us</i> Research ProgramKiran V Garimella, Qiuhui Li, Julie Wertz, et al.
American Journal of Human Genetics|April 2, 2024
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic diseaseGabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
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