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Human genomics

Showing results (1-10 of 1,247) with videos related to

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Human Genomics|October 27, 2022
DUSP5 and PHLDA1 mutations in mature cystic teratomas of the ovary identified on whole-exome sequencing may explain teratoma characteristicsWen-Chung Wang, Yen-Chein Lai
Human Genomics|November 6, 2015
Genomics is changing personal healthcare and medicine: the dawn of iPH (individualized preventive healthcare)Ruty Mehrian-Shai, Juergen K V Reichardt
Human Genomics|June 23, 2016
AMD and the alternative complement pathway: genetics and functional implicationsPerciliz L Tan, Catherine Bowes Rickman, Nicholas Katsanis
Human Genomics|June 14, 2016
Human genome meeting 2016 : Houston, TX, USA. 28 February - 2 March 2016
Human Genomics|November 19, 2014
Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataractDonna S Mackay, Thomas M Bennett, Susan M Culican, et al.
Human Genomics|August 20, 2015
Performance evaluation of indel calling tools using real short-read dataMohammad Shabbir Hasan, Xiaowei Wu, Liqing Zhang
Human Genomics|January 20, 2016
Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligamentsYichuan Liu, Yun Li, Michael E March, et al.
Human Genomics|January 9, 2016
Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibilityShannon Bruse, Michael Moreau, Yana Bromberg, et al.
Human Genomics|February 5, 2016
A review of the new HGNC gene family resourceKristian A Gray, Ruth L Seal, Susan Tweedie, et al.
Human Genomics|June 3, 2016
Systematic analysis of the molecular mechanism underlying atherosclerosis using a text mining approachDan Xi, Jinzhen Zhao, Wenyan Lai, et al.
Pageof 125

Showing results (1-10 of 1,247) with videos related to

Sort By:
Pageof 125
Human Genomics|October 27, 2022
DUSP5 and PHLDA1 mutations in mature cystic teratomas of the ovary identified on whole-exome sequencing may explain teratoma characteristicsWen-Chung Wang, Yen-Chein Lai
Human Genomics|November 6, 2015
Genomics is changing personal healthcare and medicine: the dawn of iPH (individualized preventive healthcare)Ruty Mehrian-Shai, Juergen K V Reichardt
Human Genomics|June 23, 2016
AMD and the alternative complement pathway: genetics and functional implicationsPerciliz L Tan, Catherine Bowes Rickman, Nicholas Katsanis
Human Genomics|June 14, 2016
Human genome meeting 2016 : Houston, TX, USA. 28 February - 2 March 2016
Human Genomics|November 19, 2014
Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataractDonna S Mackay, Thomas M Bennett, Susan M Culican, et al.
Human Genomics|August 20, 2015
Performance evaluation of indel calling tools using real short-read dataMohammad Shabbir Hasan, Xiaowei Wu, Liqing Zhang
Human Genomics|January 20, 2016
Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligamentsYichuan Liu, Yun Li, Michael E March, et al.
Human Genomics|January 9, 2016
Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibilityShannon Bruse, Michael Moreau, Yana Bromberg, et al.
Human Genomics|February 5, 2016
A review of the new HGNC gene family resourceKristian A Gray, Ruth L Seal, Susan Tweedie, et al.
Human Genomics|June 3, 2016
Systematic analysis of the molecular mechanism underlying atherosclerosis using a text mining approachDan Xi, Jinzhen Zhao, Wenyan Lai, et al.
Pageof 125