Haridev Aravind

Background

About Haridev Aravind

NGS Analyst specializing in germline variant interpretation, classification, and reporting with expertise in Mendelian genetics. Experienced in analyzing whole genome, exome, and targeted panels, including carrier and trio studies, and proficient in genotype–phenotype correlation using clinical databases and in silico tools. Strong background in applied genetics with the ability to communicate complex genomic findings to clinicians and contribute effectively in diagnostic genomics. Key Skills: Genomic and Plasmid DNA isolation, Replica Plating, Thin layer Chromatography, Paper Chromatography, Agarose Gel Electrophoresis, Quantification of DNA and RNA Bioinformatic tools: BLAST, BLAT, VEP, String Database, Bio-python Genome Visualization: IGV, UCSC Genome browser, Ensembl Genome Browser Databases: ClinVar, HGMD, Ensembl, HmtDB, DECIPHER, MITOMAP, Uniprot, LOVD, OMIM In-silico prediction tools: SIFT, Polyphen2, MutationTaster2, SpliceAI, FATHMM. I am eager to apply my knowledge and skills in a dynamic and forward-thinking organization, where I can contribute to breakthroughs in genetic research and biotechnology. I am actively seeking opportunities to collaborate and drive innovation in this rapidly evolving field.