Hi, I’m
Rajdeep Rajdeep
Bioinformatician
Bangalore
Summary
Demonstrated success in compiling and interpreting bioinformatics information by leveraging software, statistics and data mining. Effective at maintaining current understanding of field trends, technological advances and new computational and modeling techniques.
Overview
1
year of professional experience
1
Certificate
Work History
Karkinos Healthcare
Bioinformatician
01.2023 - Current
Job overview
- Proved successful working within tight deadlines and a fast-paced environment.
- Familiar with Linux CLI-based environments for efficient data manipulation and analysis.
- Experienced in using package managers like Anaconda to manage and deploy bioinformatics software.
- Spearheaded the discovery of the mutational landscape of HNSCC through comprehensive mutational analysis.
- Conducted cohort analysis to identify patterns and trends in genomic data, contributing to the understanding of disease mechanisms.
- Collaborated with interdisciplinary teams, including biologists and clinicians, to integrate bioinformatics findings into broader research objectives.
- Proficient in extracting and processing data from JSON and VCF files using Python and R.
Education
SASTRA Deemed UniversityThanjavur, Tamil Nadu
Master of Science from Bioinformatics
04.2001
University Overview
- Graduation with Distinction, [4th, 2nd]
- 8.01 GPA/CGPA
Adamas UniversityKolkata
Bachelor of Science from Chemistry
04.2001
University Overview
- 7.5 GPA/CGPA
Skills
Python
Certification
Bioinformatics Intern, Karkinos Healthcare - 6 months (Jan-June-2023)
Timeline
Bioinformatician
Karkinos Healthcare
01.2023 - Current
SASTRA Deemed University
Master of Science from Bioinformatics
04.2001
Adamas University
Bachelor of Science from Chemistry
04.2001
Projects
A key insight in understanding genomic alteration of Indian specific Head and Neck Squamous Cell Carcinoma cohort.
- Conducted Whole Genome Sequencing (WGS) analysis on a cohort of 39 HNSCC patient samples, unraveling the genomic landscape and identifying key somatic mutations and copy number variations (CNVs).
- Identified recurrent somatic mutations in well-known HNSCC-associated genes, such as TP53, CDKN2A, HRAS, PTEN, and PIK3CA, revealing diverse mutation patterns.
- Uncovered novel somatic mutations in genes not previously linked to HNSCC, providing new insights into the molecular mechanisms underlying the disease in the Indian population.
- Explored CNV patterns specific to the Indian cohort, utilizing advanced computational techniques to reveal unique genomic alterations associated with HNSCC.
Projects
A key insight in understanding genomic alteration of Indian specific Head and Neck Squamous Cell Carcinoma cohort.
- Conducted Whole Genome Sequencing (WGS) analysis on a cohort of 39 HNSCC patient samples, unraveling the genomic landscape and identifying key somatic mutations and copy number variations (CNVs).
- Identified recurrent somatic mutations in well-known HNSCC-associated genes, such as TP53, CDKN2A, HRAS, PTEN, and PIK3CA, revealing diverse mutation patterns.
- Uncovered novel somatic mutations in genes not previously linked to HNSCC, providing new insights into the molecular mechanisms underlying the disease in the Indian population.
- Explored CNV patterns specific to the Indian cohort, utilizing advanced computational techniques to reveal unique genomic alterations associated with HNSCC.
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