Bioinformatician
6 months ago
Perform basic data analysis and interpretation of NGS datasets, including whole genome sequencing, exome sequencing, and targeted sequencing in oncology.
2. Working on variants data generated on Thermofisher and Illumina platforms.
3. Understand role of bioinformatics tools and databases in interpretation of variants.
4. Confirmation of variants identified using genome viewers like IGV and Tablet.
5. Designing of primers for validation using Sanger Sequencing.
6. Preparing report mentioning main findings.
7. Contribute to the development and optimization of NGS data analysis workflows, ensuring high-quality and accurate results.
8. Collaborate with cross-functional teams to integrate multi-omics data and derive comprehensive insights into genetic variations and their clinical implications.
9. Generate clear and concise reports summarizing NGS findings, including variant annotations, functional impact, and potential clinical relevance.
10. Stay abreast of the latest advancements in NGS technologies, bioinformatics tools, and genomics research, actively contributing to the continuous improvement of genomic analysis processes.
11. Assist in the validation of NGS assays, ensuring adherence to quality control standards and regulatory requirements.
12. Communicate complex genomic concepts and findings effectively to both technical and non-technical audiences, fostering a collaborative and knowledge-sharing environment.
13. Performing other similar tasks assigned by reporting manager
**Job Types**: Full-time, Permanent
Pay: ₹30,000.00 - ₹60,000.00 per month
**Benefits**:
- Provident Fund
Schedule:
- Fixed shift
Supplemental pay types:
- Yearly bonus
Ability to commute/relocate:
- Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Master's (preferred)
**Experience**:
- Bioinformatics: 1 year (required)
Work Location: In person