Introduction

Attma is an opinionated, AI‑native bioinformatics assistant built on a modern Next.js front end and FastAPI orchestration layer. It takes the grind out of turning raw DNA/RNA reads, protein interaction data, and a wall of papers into something a scientist can act on before the meeting ends.

In one place you can:

• Prioritize variants (rare disease, oncology panels, emerging viral lineages) without juggling half a dozen scripts.
• Ask plain English questions and get reproducible multi‑omics comparisons – “Show differentially expressed immune escape markers between cohort A and B.”
• Surface non‑obvious patterns across sequence features, expression shifts, structural motifs for early drug target triage.
• Mine and condense fresh literature into gene–drug and pathway–phenotype relationship summaries.
• Generate clean, publication‑ready visuals and concise regulatory style summaries.

Built for real searches: genomic variant analysis, automated variant interpretation, rare disease genomics, drug discovery acceleration, bioinformatics LLM assistant, multi‑omics integration, protein structure analysis, viral mutation tracking, literature mining platform. All of that without the usual copy‑paste fatigue.

Weeks of manual bioinformatics workflow → minutes of guided, auditable analysis.

Curious? Explore the live platform: attma.bio