Robin T.Private profile: Upwork shows its earnings only to signed-in members, so we check it every few weeks, not daily. MRR here is a rough estimate (Upwork's six-month earnings ÷ months active). Last read Nov 5, 2026.

I help researchers and biotech teams turn raw sequencing data into publication-ready results: variant calls, clinical interpretation, differential expression, and figures your reviewers will accept. I'm a bioinformatics scientist at AIIMS New Delhi (Department of Pediatric Surgery), where I build and run clinical whole-exome pipelines and AI-assisted variant interpretation tools. Before AIIMS, I worked as a bioinformatics engineer at Sequentia Biotech (Spain). I hold an MSc in Computational Biology & Bioinformatics. WHAT I DELIVER - Whole-exome / whole-genome analysis: QC, alignment, GATK/Mutect2 germline and somatic calling, CNVs, VEP/ANNOVAR annotation, ACMG-based prioritization, clinical-style variant report - Bulk RNA-seq: STAR/Salmon, DESeq2/edgeR, pathway enrichment, publication figures - Single-cell RNA-seq: Cell Ranger, Seurat/Scanpy, clustering, annotation, trajectory - Pipelines: reproducible Nextflow/Snakemake workflows with Docker/Singularity, on HPC or AWS HOW I WORK - A short scoping discussion before quoting, with a fixed scope and timeline - Every project includes documented code, a methods section you can use in your manuscript, and a results report - Your data stays confidential; NDAs welcome GOOD FIT IF YOU NEED - Analysis for a manuscript, thesis or grant - A second opinion on variant calls or an RNA-seq analysis - An in-house pipeline your lab can rerun on its own Send me your data type, sample count and goal, and I'll reply within 24 hours with an approach and estimate.