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Chee Seng Ku

Showing results (11-20 of 29) with videos related to

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Public Health Genomics|November 30, 2016
The Rise and Rise of Exome SequencingChee-Seng Ku, David N Cooper, George P Patrinos
Journal of Medical Genetics|February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic diseaseChee-Seng Ku, Eng King Tan, David N Cooper
Expert Review of Molecular Diagnostics|May 24, 2012
The 'sequence everything' approach and personalized clinical decision challengesChee-Seng Ku, David N Cooper, Dimitrios H Roukos
Human Genetics|November 25, 2010
Regions of homozygosity and their impact on complex diseases and traitsChee Seng Ku, Nasheen Naidoo, Shu Mei Teo, et al.
Journal of Human Genetics|March 20, 2010
The pursuit of genome-wide association studies: where are we now?Chee Seng Ku, En Yun Loy, Yudi Pawitan, et al.
The Lancet. Oncology|April 3, 2010
Molecular epidemiology and its current clinical use in cancer managementMikael Hartman, En Yun Loy, Chee Seng Ku, et al.
Human Genomics|December 14, 2011
Human genetics and genomics a decade after the release of the draft sequence of the human genomeNasheen Naidoo, Yudi Pawitan, Richie Soong, et al.
Journal of Human Genetics|May 21, 2010
The discovery of human genetic variations and their use as disease markers: past, present and futureChee Seng Ku, En Yun Loy, Agus Salim, et al.
Bioinformatics (Oxford, England)|September 4, 2012
Statistical challenges associated with detecting copy number variations with next-generation sequencingShu Mei Teo, Yudi Pawitan, Chee Seng Ku, et al.
International Journal of Hematology|November 16, 2004
Genetic polymorphism of the CYP2C9 subfamily of 3 different races in warfarin maintenance doseGin Gin Gan, Maude Elvira Phipps, Chee Seng Ku, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Public Health Genomics|November 30, 2016
The Rise and Rise of Exome SequencingChee-Seng Ku, David N Cooper, George P Patrinos
Journal of Medical Genetics|February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic diseaseChee-Seng Ku, Eng King Tan, David N Cooper
Expert Review of Molecular Diagnostics|May 24, 2012
The 'sequence everything' approach and personalized clinical decision challengesChee-Seng Ku, David N Cooper, Dimitrios H Roukos
Human Genetics|November 25, 2010
Regions of homozygosity and their impact on complex diseases and traitsChee Seng Ku, Nasheen Naidoo, Shu Mei Teo, et al.
Journal of Human Genetics|March 20, 2010
The pursuit of genome-wide association studies: where are we now?Chee Seng Ku, En Yun Loy, Yudi Pawitan, et al.
The Lancet. Oncology|April 3, 2010
Molecular epidemiology and its current clinical use in cancer managementMikael Hartman, En Yun Loy, Chee Seng Ku, et al.
Human Genomics|December 14, 2011
Human genetics and genomics a decade after the release of the draft sequence of the human genomeNasheen Naidoo, Yudi Pawitan, Richie Soong, et al.
Journal of Human Genetics|May 21, 2010
The discovery of human genetic variations and their use as disease markers: past, present and futureChee Seng Ku, En Yun Loy, Agus Salim, et al.
Bioinformatics (Oxford, England)|September 4, 2012
Statistical challenges associated with detecting copy number variations with next-generation sequencingShu Mei Teo, Yudi Pawitan, Chee Seng Ku, et al.
International Journal of Hematology|November 16, 2004
Genetic polymorphism of the CYP2C9 subfamily of 3 different races in warfarin maintenance doseGin Gin Gan, Maude Elvira Phipps, Chee Seng Ku, et al.
Pageof 3