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Showing results (151-160 of 156) with videos related to

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The Journal of Clinical Investigation|March 26, 2011
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progressionLukas D Wartman, David E Larson, Zhifu Xiang, et al.
Nature Biotechnology|July 24, 2020
Author Correction: A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.
Nature Biotechnology|June 17, 2020
A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.
Plos Computational Biology|July 10, 2015
Genome Modeling System: A Knowledge Management Platform for GenomicsMalachi Griffith, Obi L Griffith, Scott M Smith, et al.
Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.
Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Pageof 16

Showing results (151-160 of 156) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 156 results.
The Journal of Clinical Investigation|March 26, 2011
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progressionLukas D Wartman, David E Larson, Zhifu Xiang, et al.
Nature Biotechnology|July 24, 2020
Author Correction: A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.
Nature Biotechnology|June 17, 2020
A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.
Plos Computational Biology|July 10, 2015
Genome Modeling System: A Knowledge Management Platform for GenomicsMalachi Griffith, Obi L Griffith, Scott M Smith, et al.
Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.
Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Pageof 16