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Showing results (161-170 of 225) with videos related to

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Genomics|July 21, 2010
Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotypingJinchuan Xing, W Scott Watkins, Adam Shlien, et al.
Nature Genetics|November 17, 2009
Exome sequencing identifies the cause of a mendelian disorderSarah B Ng, Kati J Buckingham, Choli Lee, et al.
Clinical Genetics|May 20, 2020
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposisBryony A Thompson, Angela K Snow, Cathryn Koptiuch, et al.
Nature Communications|August 29, 2024
Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndromeMegan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Oncotarget|December 31, 2016
Evolutionary selected Tibetan variants of HIF pathway and risk of lung cancerLucie Lanikova, N Scott Reading, Hao Hu, et al.
Human Molecular Genetics|February 11, 2022
Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palateYao Yu, Rolando Alvarado, Lauren E Petty, et al.
Plos Biology|January 14, 2014
Best practices for scientific computingGreg Wilson, D A Aruliah, C Titus Brown, et al.
Science (New York, N.Y.)|March 12, 2010
Analysis of genetic inheritance in a family quartet by whole-genome sequencingJared C Roach, Gustavo Glusman, Arian F A Smit, et al.
HGG Advances|May 24, 2025
Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopiesJocelyn N Plowman, Evanjalina J Matoy, Lavanya V Uppala, et al.
HGG Advances|May 12, 2024
Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopiesJocelyn N Plowman, Evanjalina J Matoy, Lavanya V Uppala, et al.
Pageof 23

Showing results (161-170 of 225) with videos related to

Sort By:
Pageof 23
Genomics|July 21, 2010
Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotypingJinchuan Xing, W Scott Watkins, Adam Shlien, et al.
Nature Genetics|November 17, 2009
Exome sequencing identifies the cause of a mendelian disorderSarah B Ng, Kati J Buckingham, Choli Lee, et al.
Clinical Genetics|May 20, 2020
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposisBryony A Thompson, Angela K Snow, Cathryn Koptiuch, et al.
Nature Communications|August 29, 2024
Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndromeMegan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Oncotarget|December 31, 2016
Evolutionary selected Tibetan variants of HIF pathway and risk of lung cancerLucie Lanikova, N Scott Reading, Hao Hu, et al.
Human Molecular Genetics|February 11, 2022
Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palateYao Yu, Rolando Alvarado, Lauren E Petty, et al.
Plos Biology|January 14, 2014
Best practices for scientific computingGreg Wilson, D A Aruliah, C Titus Brown, et al.
Science (New York, N.Y.)|March 12, 2010
Analysis of genetic inheritance in a family quartet by whole-genome sequencingJared C Roach, Gustavo Glusman, Arian F A Smit, et al.
HGG Advances|May 24, 2025
Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopiesJocelyn N Plowman, Evanjalina J Matoy, Lavanya V Uppala, et al.
HGG Advances|May 12, 2024
Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopiesJocelyn N Plowman, Evanjalina J Matoy, Lavanya V Uppala, et al.
Pageof 23