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Petr Danecek

Showing results (21-30 of 50) with videos related to

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Nature|May 11, 2022
Genetic and chemotherapeutic influences on germline hypermutationJoanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, et al.
American Journal of Human Genetics|October 9, 2021
Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disordersEugene J Gardner, Alejandro Sifrim, Sarah J Lindsay, et al.
Nature Communications|September 15, 2015
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panelJie Huang, Bryan Howie, Shane McCarthy, et al.
American Journal of Human Genetics|February 4, 2018
Response to GiemMarc Haber, Claude Doumet-Serhal, Christiana Scheib, et al.
American Journal of Human Genetics|August 1, 2017
Continuity and Admixture in the Last Five Millennia of Levantine History from Ancient Canaanite and Present-Day Lebanese Genome SequencesMarc Haber, Claude Doumet-Serhal, Christiana Scheib, et al.
American Journal of Human Genetics|June 2, 2015
Tracing the route of modern humans out of Africa by using 225 human genome sequences from Ethiopians and EgyptiansLuca Pagani, Stephan Schiffels, Deepti Gurdasani, et al.
Bioinformatics (Oxford, England)|December 22, 2018
Very low-depth whole-genome sequencing in complex trait association studiesArthur Gilly, Lorraine Southam, Daniel Suveges, et al.
Science (New York, N.Y.)|March 21, 2020
Insights into human genetic variation and population history from 929 diverse genomesAnders Bergström, Shane A McCarthy, Ruoyun Hui, et al.
Nature Communications|October 13, 2019
Contribution of retrotransposition to developmental disordersEugene J Gardner, Elena Prigmore, Giuseppe Gallone, et al.
Nature|November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditionsQin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Nature|May 11, 2022
Genetic and chemotherapeutic influences on germline hypermutationJoanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, et al.
American Journal of Human Genetics|October 9, 2021
Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disordersEugene J Gardner, Alejandro Sifrim, Sarah J Lindsay, et al.
Nature Communications|September 15, 2015
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panelJie Huang, Bryan Howie, Shane McCarthy, et al.
American Journal of Human Genetics|February 4, 2018
Response to GiemMarc Haber, Claude Doumet-Serhal, Christiana Scheib, et al.
American Journal of Human Genetics|August 1, 2017
Continuity and Admixture in the Last Five Millennia of Levantine History from Ancient Canaanite and Present-Day Lebanese Genome SequencesMarc Haber, Claude Doumet-Serhal, Christiana Scheib, et al.
American Journal of Human Genetics|June 2, 2015
Tracing the route of modern humans out of Africa by using 225 human genome sequences from Ethiopians and EgyptiansLuca Pagani, Stephan Schiffels, Deepti Gurdasani, et al.
Bioinformatics (Oxford, England)|December 22, 2018
Very low-depth whole-genome sequencing in complex trait association studiesArthur Gilly, Lorraine Southam, Daniel Suveges, et al.
Science (New York, N.Y.)|March 21, 2020
Insights into human genetic variation and population history from 929 diverse genomesAnders Bergström, Shane A McCarthy, Ruoyun Hui, et al.
Nature Communications|October 13, 2019
Contribution of retrotransposition to developmental disordersEugene J Gardner, Elena Prigmore, Giuseppe Gallone, et al.
Nature|November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditionsQin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.
Pageof 5