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Shweta Ramdas

Showing results (1-10 of 25) with videos related to

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NAR Genomics and Bioinformatics|February 6, 2026
ANOMALY: a Snakemake pipeline for identifying NuMTs from long-read sequencing dataNirmal S Mahar, Rachit Singh, Ishaan Gupta, et al.
Plos One|July 23, 2013
Sporulation genes associated with sporulation efficiency in natural isolates of yeastParul Tomar, Aatish Bhatia, Shweta Ramdas, et al.
Plos One|December 15, 2012
Structural, genetic, and functional signatures of disordered neuro-immunological development in autism spectrum disorderVishal Saxena, Shweta Ramdas, Courtney Rothrock Ochoa, et al.
Journal of Genetics|May 7, 2009
Investigations on possible role of MIF gene polymorphism in progression of chikungunya infection into cases of acute flaccid paralysis and chronic arthropathyShweta Ramdas Fulsundar, Subarna Roy, Sathya Prakash Manimunda, et al.
Scientific Data|April 25, 2019
Extended regions of suspected mis-assembly in the rat reference genomeShweta Ramdas, Ayse Bilge Ozel, Mary K Treutelaar, et al.
British Journal of Haematology|May 24, 2019
Genome-wide linkage analysis and whole-exome sequencing identifies an ITGA2B mutation in a family with thrombocytopeniaRami Khoriaty, Ayse B Ozel, Shweta Ramdas, et al.
Plos One|April 30, 2009
Conservation and variability of West Nile virus proteinsQi Ying Koo, Asif M Khan, Keun-Ok Jung, et al.
Oncotarget|October 21, 2017
Mutation landscape and intra-tumor heterogeneity of two MANECs of the esophagus revealed by multi-region sequencingWenqing Yuan, Zhen Liu, Wanjun Lei, et al.
BMC Medical Genomics|August 20, 2025
Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in IndiaJhanvi Shah, Debasrija Mondal, Deepika Jain, et al.
American Journal of Human Genetics|February 6, 2026
Expanded chromatin accessibility mapping explains genetic variation associated with complex traits in liverBrandon M Wenz, Max F Dudek, Shweta Ramdas, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
NAR Genomics and Bioinformatics|February 6, 2026
ANOMALY: a Snakemake pipeline for identifying NuMTs from long-read sequencing dataNirmal S Mahar, Rachit Singh, Ishaan Gupta, et al.
Plos One|July 23, 2013
Sporulation genes associated with sporulation efficiency in natural isolates of yeastParul Tomar, Aatish Bhatia, Shweta Ramdas, et al.
Plos One|December 15, 2012
Structural, genetic, and functional signatures of disordered neuro-immunological development in autism spectrum disorderVishal Saxena, Shweta Ramdas, Courtney Rothrock Ochoa, et al.
Journal of Genetics|May 7, 2009
Investigations on possible role of MIF gene polymorphism in progression of chikungunya infection into cases of acute flaccid paralysis and chronic arthropathyShweta Ramdas Fulsundar, Subarna Roy, Sathya Prakash Manimunda, et al.
Scientific Data|April 25, 2019
Extended regions of suspected mis-assembly in the rat reference genomeShweta Ramdas, Ayse Bilge Ozel, Mary K Treutelaar, et al.
British Journal of Haematology|May 24, 2019
Genome-wide linkage analysis and whole-exome sequencing identifies an ITGA2B mutation in a family with thrombocytopeniaRami Khoriaty, Ayse B Ozel, Shweta Ramdas, et al.
Plos One|April 30, 2009
Conservation and variability of West Nile virus proteinsQi Ying Koo, Asif M Khan, Keun-Ok Jung, et al.
Oncotarget|October 21, 2017
Mutation landscape and intra-tumor heterogeneity of two MANECs of the esophagus revealed by multi-region sequencingWenqing Yuan, Zhen Liu, Wanjun Lei, et al.
BMC Medical Genomics|August 20, 2025
Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in IndiaJhanvi Shah, Debasrija Mondal, Deepika Jain, et al.
American Journal of Human Genetics|February 6, 2026
Expanded chromatin accessibility mapping explains genetic variation associated with complex traits in liverBrandon M Wenz, Max F Dudek, Shweta Ramdas, et al.
Pageof 3