Introduction

Key Features

• Upload raw DNA sequencing data (FASTA, FASTQ, or plain text) and let the platform process every file automatically.
• Align your reads against reference genomes and inspect alignment ranges, confidence scores, and base-by-base differences.
• Automated cancer candidate detection that compares each new sample against past samples of the same individual.
• Automated CRISPR-Cas9 gene therapy guide design for every detected mutation and variant.
• An Ask AI assistant that answers questions about your genomes, alignments, variants, and genes — with persisted conversations.
• Notifications, threaded alignment comments, and granular account controls (individuals, genomes, settings, and data deletion).

Explore the Documentation

Detailed guides for every part of the platform:

• Individuals — Organize the people and samples you analyze.
• Genomes — Upload DNA sequences and follow their processing status.
• Alignments — Understand alignments, ranges, confidence, and comments.
• Cancer Candidates — Review detected mutations, severity, certainty, and gene therapy guides.
• Ask AI — Chat with the AI assistant and manage your conversations.
• Notifications & Activity — Learn how job and activity notifications work.
• Settings — Manage your profile, password, individuals, and account data.
• Subscriptions & Plans — Choose a plan and manage your subscription and billing.
• User Data Deletion — Understand exactly what happens when you delete your data.

Who Is It For?

GENOTURK is built for individuals and families who want to understand their genetic data, bioinformatics hobbyists, laboratories and research institutions who want to analyze genomes without expensive laboratory equipment or complex command-line pipelines.

Getting Started