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Sumit Middha

Showing results (21-30 of 80) with videos related to

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Bioinformatics (Oxford, England)|June 13, 2012
SAAP-RRBS: streamlined analysis and annotation pipeline for reduced representation bisulfite sequencingZhifu Sun, Saurabh Baheti, Sumit Middha, et al.
Familial Cancer|April 14, 2017
Universal screening for microsatellite instability in colorectal cancer in the clinical genomics era: new recommendations, methods, and considerationsJaclyn F Hechtman, Sumit Middha, Zsofia K Stadler, et al.
Human Pathology|August 20, 2018
Somatic HNF1A mutations in the malignant transformation of hepatocellular adenomas: a retrospective analysis of data from MSK-IMPACT and TCGAJaclyn F Hechtman, Ghassan K Abou-Alfa, Zsofia K Stadler, et al.
The Prostate|August 12, 2014
Mutational landscape of candidate genes in familial prostate cancerAnna M Johnson, Kimberly A Zuhlke, Chris Plotts, et al.
Molecular Endocrinology (Baltimore, Md.)|June 27, 2012
Research resource: whole transcriptome RNA sequencing detects multiple 1α,25-dihydroxyvitamin D(3)-sensitive metabolic pathways in developing zebrafishTheodore A Craig, Yuji Zhang, Melissa S McNulty, et al.
American Journal of Human Genetics|May 19, 2015
Comprehensively evaluating cis-regulatory variation in the human prostate transcriptome by using gene-level allele-specific expressionNicholas B Larson, Shannon McDonnell, Amy J French, et al.
Neurology|February 7, 2014
Ubiquitin ligase defect by DCAF8 mutation causes HMSN2 with giant axonsChristopher J Klein, Yanhong Wu, Peter Vogel, et al.
Investigative Ophthalmology & Visual Science|August 30, 2014
Comprehensive assessment of genetic variants within TCF4 in Fuchs' endothelial corneal dystrophyEric D Wieben, Ross A Aleff, Bruce W Eckloff, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 8, 2014
Application of whole exome sequencing in undiagnosed inherited polyneuropathiesChristopher J Klein, Sumit Middha, Xiaohui Duan, et al.
The Journal of Pathology|July 19, 2017
The genetic landscape of endometrial clear cell carcinomasDeborah F DeLair, Kathleen A Burke, Pier Selenica, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Bioinformatics (Oxford, England)|June 13, 2012
SAAP-RRBS: streamlined analysis and annotation pipeline for reduced representation bisulfite sequencingZhifu Sun, Saurabh Baheti, Sumit Middha, et al.
Familial Cancer|April 14, 2017
Universal screening for microsatellite instability in colorectal cancer in the clinical genomics era: new recommendations, methods, and considerationsJaclyn F Hechtman, Sumit Middha, Zsofia K Stadler, et al.
Human Pathology|August 20, 2018
Somatic HNF1A mutations in the malignant transformation of hepatocellular adenomas: a retrospective analysis of data from MSK-IMPACT and TCGAJaclyn F Hechtman, Ghassan K Abou-Alfa, Zsofia K Stadler, et al.
The Prostate|August 12, 2014
Mutational landscape of candidate genes in familial prostate cancerAnna M Johnson, Kimberly A Zuhlke, Chris Plotts, et al.
Molecular Endocrinology (Baltimore, Md.)|June 27, 2012
Research resource: whole transcriptome RNA sequencing detects multiple 1α,25-dihydroxyvitamin D(3)-sensitive metabolic pathways in developing zebrafishTheodore A Craig, Yuji Zhang, Melissa S McNulty, et al.
American Journal of Human Genetics|May 19, 2015
Comprehensively evaluating cis-regulatory variation in the human prostate transcriptome by using gene-level allele-specific expressionNicholas B Larson, Shannon McDonnell, Amy J French, et al.
Neurology|February 7, 2014
Ubiquitin ligase defect by DCAF8 mutation causes HMSN2 with giant axonsChristopher J Klein, Yanhong Wu, Peter Vogel, et al.
Investigative Ophthalmology & Visual Science|August 30, 2014
Comprehensive assessment of genetic variants within TCF4 in Fuchs' endothelial corneal dystrophyEric D Wieben, Ross A Aleff, Bruce W Eckloff, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 8, 2014
Application of whole exome sequencing in undiagnosed inherited polyneuropathiesChristopher J Klein, Sumit Middha, Xiaohui Duan, et al.
The Journal of Pathology|July 19, 2017
The genetic landscape of endometrial clear cell carcinomasDeborah F DeLair, Kathleen A Burke, Pier Selenica, et al.
Pageof 8