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Celine S Hong

Showing results (1-10 of 8) with videos related to

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BMC Bioinformatics|March 7, 2021
SomatoSim: precision simulation of somatic single nucleotide variantsMarwan A Hawari, Celine S Hong, Leslie G Biesecker
Genome Medicine|August 10, 2016
Assessing the reproducibility of exome copy number variations predictionsCeline S Hong, Larry N Singh, James C Mullikin, et al.
Plos One|March 3, 2011
A computational method for prediction of excretory proteins and application to identification of gastric cancer markers in urineCeline S Hong, Juan Cui, Zhaohui Ni, et al.
Human Molecular Genetics|August 22, 2023
Genome-wide identification of dominant polyadenylation hexamers for use in variant classificationHenoke K Shiferaw, Celine S Hong, David N Cooper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 19, 2016
Assessing the capability of massively parallel sequencing for opportunistic pharmacogenetic screeningDavid Ng, Celine S Hong, Larry N Singh, et al.
BMC Bioinformatics|April 9, 2021
Low-level variant calling for non-matched samples using a position-based and nucleotide-specific approachJeffrey N Dudley, Celine S Hong, Marwan A Hawari, et al.
International Journal of Cancer|November 26, 2014
Comprehensive characterization of the genomic alterations in human gastric cancerJuan Cui, Yanbin Yin, Qin Ma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2017
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centersRashesh V Sanghvi, Christian J Buhay, Bradford C Powell, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
BMC Bioinformatics|March 7, 2021
SomatoSim: precision simulation of somatic single nucleotide variantsMarwan A Hawari, Celine S Hong, Leslie G Biesecker
Genome Medicine|August 10, 2016
Assessing the reproducibility of exome copy number variations predictionsCeline S Hong, Larry N Singh, James C Mullikin, et al.
Plos One|March 3, 2011
A computational method for prediction of excretory proteins and application to identification of gastric cancer markers in urineCeline S Hong, Juan Cui, Zhaohui Ni, et al.
Human Molecular Genetics|August 22, 2023
Genome-wide identification of dominant polyadenylation hexamers for use in variant classificationHenoke K Shiferaw, Celine S Hong, David N Cooper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 19, 2016
Assessing the capability of massively parallel sequencing for opportunistic pharmacogenetic screeningDavid Ng, Celine S Hong, Larry N Singh, et al.
BMC Bioinformatics|April 9, 2021
Low-level variant calling for non-matched samples using a position-based and nucleotide-specific approachJeffrey N Dudley, Celine S Hong, Marwan A Hawari, et al.
International Journal of Cancer|November 26, 2014
Comprehensive characterization of the genomic alterations in human gastric cancerJuan Cui, Yanbin Yin, Qin Ma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2017
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centersRashesh V Sanghvi, Christian J Buhay, Bradford C Powell, et al.
Pageof 1