- Analysis and detailed interpretation of genomic data of NGS/Sanger sequencing of clinical cases
- Identification and annotating the variants with their potential functional significance, knowledge of relevant therapies, literature review and writing detailed reports
- Knowledge of cancer genomics and reproductive genomics
- Knowledge of current and recent softwares for analysis of genomic data
- Designing primers
- Maintaining TAT for the assigned test reports
Working with-Sr. Genome Analyst
What the role entails Key accountabilities/ responsibilities
- Genomic Data Interpretation: Analyze and interpret genomic data from NGS and Sanger sequencing, ensuring accurate insights for clinical casework.
- Variant Annotation & Reporting: Identify, annotate, and interpret genetic variants with functional significance; compile detailed clinical reports supported by literature and relevant therapeutic information.
- Domain Expertise: Apply sound knowledge in cancer genomics and reproductive genomics for case analysis and result interpretation.
- Bioinformatics Tools & Software:
Utilize current and emerging software tools for efficient and accurate genomic data analysis.
- Primer Design: Design primers for molecular assays with precision and adherence to test protocols.
- TAT Compliance: Ensure timely delivery of test reports by maintaining turnaround time (TAT) standards for all assigned cases.
What we are looking for in you- MSc with 3-4 yrs experience
Role Demands (travel)- No/Yes
Location-Vidyavihar
Requirement Education
Essential- Post Graduate Certificate Course in Medical and Genetic Counselling /MSC in Biotechnology
Experience- 4 to 6 Years
Role: Healthcare & Life Sciences - Other, Industry Type: Medical Services / Hospital (Diagnostics), Department: Healthcare & Life Sciences, Employment Type: Full Time, Permanent Role Category: Healthcare & Life Sciences - Other Education UG: B.Sc in Bioinformatics, Genetics, Biotechnology PG: MS/M.Sc(Science) in Biotechnology Key Skills Skills highlighted with ‘‘ are preferred keyskills Primer DesigningVariant AnnotationGenomicsNgsBioinformatics RT-PCRGeneticsSequencing