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Darshana R

Darshana R

Genome Analyst

Talent
KarnatakaMember since April 11, 2026
NGS Data AnalysisLinux Shell ScriptingPythonGenomic Data AnalysisVariant Calling and CurationCopy Number Variations (CNV) AnalysisGene Fusion DetectionMetagenomicsClinical Report GenerationDatabase Annotation (ClinVar, COSMIC, dbSNP)Microsoft ExcelMicrosoft PowerPointMicrosoft WordLinux Operating SystemBioinformatic PipelinesQuality Control (QC)ACMG/AMP Clinical InterpretationIn-silico Predictors (CADD, SIFT, PolyPhen-2, MutationTaster)
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NGS Data AnalysisLinux Shell ScriptingPythonGenomic Data AnalysisVariant Calling and Curation

About

Motivated and detail-oriented Genome Analyst Trainee with proven expertise in genomic data analysis, bioinformatics tools, and management of large-scale datasets. Skilled in analyzing raw genomic data, identifying cancer-related mutations, copy number variations, and gene fusions to support precision oncology initiatives. Proficient in Linux shell scripting and advanced quality control methodologies.

Demonstrates strong collaboration with cross-functional teams, meticulous attention to detail, and adherence to industry standards, delivering high-quality data reporting and contributing meaningfully to personalized treatment strategies in precision medicine.

Experience

Genome Analyst Trainee at 4Basecare Precision Health Pvt Ltd (2024-07 – Present)

End-to-end analysis of processed NGS data from FFPE tumor tissue for precision oncology and cancer genomics.

  • Performed end-to-end analysis of processed NGS data from FFPE tumor tissue, achieving >350X mean coverage and >1000X total depth for a 1212-gene comprehensive oncology panel.
  • Executed somatic variant calling and curation across SNVs, InDels, CNVs, splice variants, fusions, TMB, and MSI, followed by rigorous QC and allele burden assessment per variant.
  • Applied standardized clinical interpretation frameworks (ACMG/AMP, ASCO, AMP, NCCN, ESMO, FDA) to tier and report clinically relevant alterations and VUS with literature-backed rationale.
  • Conducted database-driven annotation and population filtering using ClinVar, COSMIC, dbSNP, 1000 Genomes, ExAC/gnomAD, and in-silico predictors (CADD, SIFT, PolyPhen-2, MutationTaster).
  • Demonstrated strong attention to detail in all aspects of NGS data analysis, QC processes, and result validation for enhanced diagnostic accuracy.

Bioinformatics Intern - Department of Genome Informatics at Genotypic Technology Pvt Ltd (2024-01 – 2024-06)

Conducted targeted and whole-genome metagenomic analysis using Next Generation Sequencing technologies with focus on bioinformatics data processing and optimization.

  • Conducted targeted and whole-genome metagenomic analysis using Next Generation Sequencing (NGS) technologies, enhancing the scope and accuracy of genetic research projects.
  • Performed comprehensive bioinformatics analyses on metagenomic datasets, including quality control, taxonomy classification, functional annotation, and diversity metrics computation, ensuring high-quality and reliable data outputs.
  • Optimised Linux shell scripts, leading to a 25% increase in data processing efficiency, and streamlining bioinformatics workflows.

Education

Master of Science in Bioinformatics – Manipal School of Life Sciences

Bachelor of Science in Chemistry, Zoology, Microbiology – Mount Carmel College

Skills

Genome Analyst

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