Building a community space that enables epistemic & emotional growth while inspiring impactful work on local & global catastrophic risks.

Built and managed the development of the iCare platform, enabling oncologists to understand the mutational profiles of their patients and suggest appropriate cancer therapies.

• Gathered requirements from various stakeholders and translated them into appropriate user interfaces and pipelines.
• Led a team of software developers and bioinformaticians on various projects within iCare.
• Designed interactive user interfaces and robust bioinformatics pipelines for flagship products such as OncoDx and OncoPredikt.
• Oversaw and executed deployment activities, ensuring smooth transitions through all phases of the software development lifecycle (SDLC).

Built a web app from scratch that identifies and annotates rare mutations in cancer patients, providing an interactive interface for oncologists to track patients and discover appropriate treatments.

As the solo developer for a lab trying to cure spinal cord injury, I designed and developed multiple bioinformatics piplines and web tools that provide novel insights in genetic and epigenetic regulation behind axon growth.

• Developed bioinformatics pipelines that discovered novel transcription factor combinations regulating axon growth.
• Created a web tool that allows scientists to visualize ATAC-Seq, RNA-seq and Histone Chip-Seq datasets across different time points in development of mice.
• Developed a website that visualizes and quantifies supra spinal neurons with projections to the cervical, thoracic and lumbar segments.

Developed a tool for the Rat Genome database that provides a unique way to seamlessly visualize and perform set operations on lists of genes.

• Developed web-based tools using the Flask framework, that automate and simplify the Bioinformatics workflow of Molecular Diagnostics Lab
• Human clinical genomics - Monitored NGS workflow, develop variant calling and variant annotation pipelines
• Designed and created an interactive web tool VIRAS, that provides a graphical view to analyze nucleotide mismatches between patients 10.1016/j.bbmt.2018.12.006
• Developed data visualization tools using d3.js to help investigators analyze NGS workflow and patient report data

Developed custom shell scripts that automate RNA-Seq, and ChIP-Seq workflows

Designed & developed SNPredict, a tool that predicts rare somatic variants using multiple machine learning training algorithms like kNN & LinearSVC

Lead production support duties. Designed, coded and maintained Bash shell scripts to automate tasks for checking and updating status of AT&T servers.