Area of research
Cancer Research · Infectious Diseases
Research interest
Research interests include Cancer-related molecular mechanisms research, SARS-CoV-2 and COVID-19 Research, RNA modifications and cancer, and Genomics and Rare Diseases.
Genetic Spectrum of Autism Spectrum Disorder Associated Variants in the Indian Population: Insights from 1,029 IndiGenomes
Decoding the genetic symphony: Profiling protein-coding and long noncoding RNA expression in T-acute lymphoblastic leukemia for clinical insights.
The genomic landscape of <i>CYP2D6</i> variation in the Indian population.
SCAR-6 elncRNA locus epigenetically regulates PROZ and modulates coagulation and vascular function.
Syntenic lncRNAs exhibit DNA regulatory functions with sequence evolution
A Rapid and Scalable Multiplex PCR-Based Next-Generation Amplicon Sequencing Method for Familial Hypercholesterolemia Genetic Screening.
<i>SCAR-6</i> elncRNA locus epigenetically regulates <i>PROZ</i> and modulates coagulation and vascular function
LncRNA <i>TAAL</i> is a Modulator of <i>Tie1</i> -Mediated Vascular Function in Diabetic Retinopathy
An amplicon-based approach for fast and scalable genome sequencing of lumpy skin disease virus on benchtop next-generation sequencers
An <i>Alu</i> insertion map of the Indian population: identification and analysis in 1021 genomes of the IndiGen project.
SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion
LncRNA VEAL2 regulates PRKCB2 to modulate endothelial permeability in diabetic retinopathy.
An optimized, amplicon-based approach for sequencing of SARS-CoV-2 from patient samples using COVIDSeq assay on Illumina MiSeq sequencing platforms.
Insights from Genomes and Genetic Epidemiology of SARS-CoV-2 isolates from the state of Andhra Pradesh
A genome-wide circular RNA transcriptome in rat.
High throughput detection and genetic epidemiology of SARS-CoV-2 using COVIDSeq next generation sequencing
Genetic epidemiology of variants associated with immune escape from global SARS-CoV-2 genomes
Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding
Exome sequencing of patients with histiocytoid cardiomyopathy reveals a de novo <i>NDUFB11</i> mutation that plays a role in the pathogenesis of histiocytoid cardiomyopathy
Barcoding of Asian seabass across its geographic range provides evidence for its bifurcation into two distinct species