Supreet Kaur Email & Phone Number

Bengaluru, Karnataka, India

-Interpreted and reported sequenced sample data for various cancer types, including solid tumors and hematological cancers, using a proprietary NGS platform.-Identified genomic alterations linked to disease progression and treatment response, creating detailed clinical reports.-Utilized bioinformatics tools, databases (UCSC, gnomAD, ClinVar, COSMIC, CKB-JAX, HGMD) and guidelines (NCCN and ACMG) to ensure accurate annotation and classification of complex genomic variants, providing precise clinical recommendations.-Supported international clients by enhancing their scientific databases and sharing insights to improve diagnostic decisions and patient care in oncology.

Bengaluru, Karnataka, India

-Analyzed the clinical relevance of gene variants identified through diverse sequencing methods within a clinical laboratory environment. This involved a comprehensive assessment of data sourced from both internal and external databases, as well as pertinent research papers.-Interpreted the therapeutic and prognostic significance of genomic variants in cancer, curating essential information for a client database. This included synthesizing complex data to provide actionable insights for clinical decision-making.-Contributed to the curation of World Health Organization (WHO) guidelines for various cancer types, meticulously distinguishing data based on diagnostic, therapeutic, and prognostic relevance. This effort aimed to streamline the understanding and application of guidelines in clinical practice.-Maintained and regularly updated an internal database with variant information to facilitate the delivery of precise and effective treatment options, including targeted therapies and ongoing clinical trials. This involved ensuring the accessibility of up-to-date information for clients, hospitals, and clinicians, enabling informed decision-making.

Bengaluru, Karnataka, India

-Trained extensively in clinical interpretation and genomic data analysis, specializing in the dynamic field of cancer research.-Proficient in the clinical interpretation of somatic variants, contributing to the advancement of clinical genomics content. Basically, performed in-depth analysis of somatic variants in cancer patient samples, assessing their functional implications and relevance both at clinical & preclinical level.-Actively involved in the curation process, meticulously selecting genes, somatic variants, and establishing gene-disease correlations in various solid and hematological cancers. -Leveraged public databases (PubMed, OncoKB, JAX CKB, Uniprot, Ensembl, COSMIC), published scientific literature and bioinformatic tools to enrich a comprehensive client database, ensuring accuracy and relevance.-Demonstrated expertise in curating mutation-based FDA drug approvals, clinical trial results, and abstracts from reputable conferences such as ASCO, ESMO, ASH, and AACR.-Skilled in gathering and organizing functional, clinical, preclinical, and prognostic data, along with treatment guidelines, to provide a holistic understanding of somatic cancer variants.

Msc - Master Of Science, Microbiology, Cgpa 7.86

Relevant Subjects:- Microbial Genetics, Molecular Biology, Food Microbiology, Environmental Biology, Bioinformatics, Molecular Biology.

Bsc - Bachelor Of Science, Biotechnology, Biochemistry And Genetics, Cgpa 8.30

Intermediate, Physics, Chemistry, Biology, English And Hindi, 77%

High School, Science, Mathematics,English, Hindi And Social Studies, 76%

Activities and Societies: Participated in GREEN OLYMPIAD organised by TERI Represented my school at Patna in Science Exhibition