K V Meghana

M.Sc.

Applied

Genetics graduate with 2.5 years of experience in oncology clinical data review and genetic report interpretation. Experienced in analyzing genetic test reports, identifying clinically relevant variants, and ensuring high-quality data accuracy. Recently trained in bioinformatics workflows including NGS data concepts, sequence analysis, and variant interpretation using tools like NCBI, ClinVar, BLAST, and OMIM.

Strong analytical mindset with attention to detail and interest in genomic data analysis, variant interpretation, and clinical reporting.

Medical Reviewer - Omega Healthcare

(2023-12)

• Performed clinical data abstraction and analysis of oncology patient records, including genetic testing reports
• Reviewed and interpreted genetic panel reports (NGS-based and other platforms) for multiple cancers (lung, breast, prostate, ovarian)
• Identified variants, mutations, and clinically relevant alterations from Various genomic reports.
• Ensured accuracy, consistency, and quality control (QC) of clinical and genetic data
• Collaborated with internal teams to resolve discrepancies and maintain data integrity
• Maintained strict adherence to SOPs, timelines, and quality benchmarks

Genetic Counseling Intern - Narayana Health city

(2022-12 - 2023-01)

Internship in Clinical Genetics under Dr. SJ Patil.

• Pedigree analysis and patient history collection
• Assisted in counseling sessions and consent process
• Participated in wet lab activities including karyotyping for chromosomal analysis
• Conducted case presentations involving clinical history, pedigree construction, and genetic interpretation

M.Sc Applied Genetics - Applied Genetics (2021 - 2023)

B.Sc BZC - BZC (2018 - 2021)