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Ryan E Mills

Showing results (51-60 of 67) with videos related to

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Nature Genetics|April 6, 2010
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencingHansoo Park, Jong-Il Kim, Young Seok Ju, et al.
Scientific Data|November 20, 2023
Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseasesMcKinzie A Garrison, Yeongjun Jang, Taejeong Bae, et al.
Oncotarget|November 23, 2017
Rapid, ultra low coverage copy number profiling of cell-free DNA as a precision oncology screening strategyDaniel H Hovelson, Chia-Jen Liu, Yugang Wang, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Multi-platform framework for mapping somatic retrotransposition in human tissuesSeunghyun Wang, Mingyun Bae, Jinhao Wang, et al.
Science (New York, N.Y.)|April 29, 2017
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism NetworkMichael J McConnell, John V Moran, Alexej Abyzov, et al.
Nature|July 10, 2009
A highly annotated whole-genome sequence of a Korean individualJong-Il Kim, Young Seok Ju, Hansoo Park, et al.
Genome Biology|March 30, 2021
Comprehensive identification of somatic nucleotide variants in human brain tissueYifan Wang, Taejeong Bae, Jeremy Thorpe, 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.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
Nature Genetics|April 6, 2010
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencingHansoo Park, Jong-Il Kim, Young Seok Ju, et al.
Scientific Data|November 20, 2023
Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseasesMcKinzie A Garrison, Yeongjun Jang, Taejeong Bae, et al.
Oncotarget|November 23, 2017
Rapid, ultra low coverage copy number profiling of cell-free DNA as a precision oncology screening strategyDaniel H Hovelson, Chia-Jen Liu, Yugang Wang, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Multi-platform framework for mapping somatic retrotransposition in human tissuesSeunghyun Wang, Mingyun Bae, Jinhao Wang, et al.
Science (New York, N.Y.)|April 29, 2017
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism NetworkMichael J McConnell, John V Moran, Alexej Abyzov, et al.
Nature|July 10, 2009
A highly annotated whole-genome sequence of a Korean individualJong-Il Kim, Young Seok Ju, Hansoo Park, et al.
Genome Biology|March 30, 2021
Comprehensive identification of somatic nucleotide variants in human brain tissueYifan Wang, Taejeong Bae, Jeremy Thorpe, 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.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
Pageof 7