Tahseen Arif

I am a dedicated and result-oriented Genome Analyst with over 2 years of experience in Next Generation Sequencing (NGS) data analysis. My expertise includes Clinical Exome, Whole Exome, Whole Genome, Whole Mitochondrial genome, Couple Screening, and Trio Analysis. I have a strong background in variant interpretation, utilizing standard ACMG guidelines to classify variants based on pathogenicity.

At MedGenome Labs Ltd, I honed my skills in identifying and annotating genetic variants using various bioinformatics tools. I am proficient in variant prioritization, focusing on functional impact, population frequency, and disease relevance. My ability to read and interpret scientific literature allows me to curate relevant findings clearly and concisely, contributing to the management of clinical reports for germline and rare-Mendelian disorders.