Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Bharathram Uppili

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Database : the Journal of Biological Databases and Curation|April 11, 2024
STRIDE-DB: a comprehensive database for exploration of instability and phenotypic relevance of short tandem repeats in the human genomeBharathram Uppili, Mohammed Faruq
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|September 12, 2018
EasyQC: Tool with Interactive User Interface for Efficient Next-Generation Sequencing Data Quality ControlVijaya Raghavan Rangamaran, Bharathram Uppili, Dharani Gopal, et al.
Human Genome Variation|June 13, 2024
Identifying unstable CNG repeat loci in the human genome: a heuristic approach and implications for neurological disordersVarun Suroliya, Bharathram Uppili, Manish Kumar, et al.
Clinical Genetics|February 4, 2025
Genome-Wide Association Study Reveals Genetic Architecture of Common EpilepsiesSarita Thakran, Debleena Guin, Priyanka Singh, et al.
The Journal of Gene Medicine|March 3, 2018
A novel mutation in SLC39A14 causing hypermanganesemia associated with infantile onset dystoniaMonica Juneja, Uzma Shamim, Aditi Joshi, et al.
Brain Communications|April 3, 2023
Sequencing through hyperexpanded Friedreich's ataxia-GAA repeats by nanopore technology: implications in genotype-phenotype correlationBharathram Uppili, Pooja Sharma, Istaq Ahmad, et al.
Molecular Genetics and Metabolism Reports|July 20, 2018
A novel mutation in SGSH causing Sanfillipo type 3A Mucopolysaccharidoses in an Indian familyJyotsna Singh, P K Muhammad, Sweta Jain, et al.
Neurogenetics|November 2, 2023
Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohortNishu Tyagi, Bharathram Uppili, Pooja Sharma, et al.
Vaccines|January 22, 2022
Vaccine Breakthrough Infections by SARS-CoV-2 Variants after ChAdOx1 nCoV-19 Vaccination in Healthcare WorkersPratibha Kale, Ekta Gupta, Chhagan Bihari, et al.
Journal of Medical Virology|March 22, 2021
Reinfection or reactivation: Genome-based two distinct SNP profile of SARS-CoV2 repositivity in an Indian caseMahesh S Dhar, Vivekanand Asokachandran, Bharathram Uppili, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Database : the Journal of Biological Databases and Curation|April 11, 2024
STRIDE-DB: a comprehensive database for exploration of instability and phenotypic relevance of short tandem repeats in the human genomeBharathram Uppili, Mohammed Faruq
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|September 12, 2018
EasyQC: Tool with Interactive User Interface for Efficient Next-Generation Sequencing Data Quality ControlVijaya Raghavan Rangamaran, Bharathram Uppili, Dharani Gopal, et al.
Human Genome Variation|June 13, 2024
Identifying unstable CNG repeat loci in the human genome: a heuristic approach and implications for neurological disordersVarun Suroliya, Bharathram Uppili, Manish Kumar, et al.
Clinical Genetics|February 4, 2025
Genome-Wide Association Study Reveals Genetic Architecture of Common EpilepsiesSarita Thakran, Debleena Guin, Priyanka Singh, et al.
The Journal of Gene Medicine|March 3, 2018
A novel mutation in SLC39A14 causing hypermanganesemia associated with infantile onset dystoniaMonica Juneja, Uzma Shamim, Aditi Joshi, et al.
Brain Communications|April 3, 2023
Sequencing through hyperexpanded Friedreich's ataxia-GAA repeats by nanopore technology: implications in genotype-phenotype correlationBharathram Uppili, Pooja Sharma, Istaq Ahmad, et al.
Molecular Genetics and Metabolism Reports|July 20, 2018
A novel mutation in SGSH causing Sanfillipo type 3A Mucopolysaccharidoses in an Indian familyJyotsna Singh, P K Muhammad, Sweta Jain, et al.
Neurogenetics|November 2, 2023
Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohortNishu Tyagi, Bharathram Uppili, Pooja Sharma, et al.
Vaccines|January 22, 2022
Vaccine Breakthrough Infections by SARS-CoV-2 Variants after ChAdOx1 nCoV-19 Vaccination in Healthcare WorkersPratibha Kale, Ekta Gupta, Chhagan Bihari, et al.
Journal of Medical Virology|March 22, 2021
Reinfection or reactivation: Genome-based two distinct SNP profile of SARS-CoV2 repositivity in an Indian caseMahesh S Dhar, Vivekanand Asokachandran, Bharathram Uppili, et al.
Pageof 2