About
B.Tech Biotechnology graduate pursuing an Advanced Diploma in Bioinformatics, with practical training in NGS, genomic data analysis, sequence analysis, and variant analysis. Experienced with R, Python/Biopython, Linux/Bash, and bioinformatics databases and workflows, and seeking an entry-level role in bioinformatics and computational genomics.
Experience
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Research InternHelix Biogenesis Pvt. Ltd. · Noida, Uttar PradeshJul 2025 – Sep 2025
Performed core laboratory procedures including DNA isolation, PCR amplification and microbial culture workflows. Applied aseptic technique and laboratory safety protocols while maintaining accurate experimental documentation and records.
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Internship TraineeRapture Biotech International Pvt. Ltd. · Noida, Uttar PradeshJul 2025 – Aug 2025
Trained across biochemistry, immunology and cell biology laboratory techniques, gaining hands-on exposure to core wet-lab methods. Performed enzyme assays and protein analysis while maintaining accurate experiment records and documentation.
Education
- 2026
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2026
Advanced Diploma in BioinformaticsWin In Life AcademyAwarded by CliniLaunch Research Institute / Win In Life AcademyBioinformatics · Jun 2026
Skills
Tools / apps / platforms
Projects
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Protein–Ligand Molecular Docking of PQQ with Quinoprotein Glucose DehydrogenaseAutoDock Vina, SwissDock, PDB, PyMOL, UCSF Chimera
Docked PQQ against quinoprotein glucose dehydrogenase and analyzed binding poses and protein–ligand interactions to assess docking outcomes.
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Global Sequence Alignment — Needleman–Wunsch AlgorithmPython
Implemented the Needleman–Wunsch dynamic programming algorithm to align nucleotide sequences and verify alignment scores and sequence identity.
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Linux-Based FASTA Sequence ProcessingLinux, awk, Bash
Merged multiple FASTA files using Linux command-line utilities, counted and cross-verified sequence records with awk, and automated repetitive sequence-handling tasks using Bash scripting.
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NGS & Genomic Data AnalysisNCBI, SRA, GEO, RefSeq
Processed NGS datasets and genomic data formats to practice sequence analysis, variant calling, and genome annotation workflows. Queried dbSNP and explored population genomics datasets to interpret variant frequency data.