AI-Assisted Genomic Intelligence:
From Sequencing
Data To Clinical Report
Seq2Clin is Yukti Genomic's flagship platform for genomic data interpretation, evidence-linked reporting and clinical review workflow automation.
It is designed to help diagnostic labs and hospitals transform sequencing outputs into structured, clinician-ready reports across oncology, germline, rare disease, hereditary conditions and pharmacogenomics.
THE PROBLEM
Modern sequencing can generate vast amounts of genomic data. But turning that data into clinically meaningful insight remains difficult.
Modern sequencing can generate vast amounts of genomic data. But turning that data into clinically meaningful insight remains difficult.
WHAT Seq2Clin DOES
A Platform For Post
Sequencing Intelligence
FASTQ, BAM and VCF
workflow support for all sequencers
Variant annotation and
prioritization
Oncology actionability
support
Evidence-linked
interpretation
Gene, disease and
phenotype association
mapping
Germline and
hereditary disease
interpretation support
Rare disease
workflows
Pharmacogenomics
interpretation support
Report generation and
template customization
Expert review and QA
workflow support
Audit-ready evidence
traceability
Future-ready API and
integration architecture
HOW Seq2Clin WORKS
From Raw Genomic Data To Clinical-Ready Insights
Seq2Clin automates the journey from sequencing data to clinical interpretation, By processing FASTQ, BAM, and VCF files through an intelligent analysis pipeline, it delivers accurate, standardized, and actionable genomic reports that support confident diagnostic and treatment decisions.
Seq2Clin is a comprehensive Clinical Intelligence Platform composed of 'Six' specialized intelligence engines that together power precision medicine.
Enable seamless analysis from sequencing data to clinical insights. Supports growing genomic programs with streamlined workflows.
Genomic Analysis Workspace
Seq2Clin Analyze FASTQ/BAM/VCF workflows; bioinformatics-light labs; growing NGS programs; labs expanding into WES or larger panels. Integrated analysis-to-report workflow support.
Integrated analysis-to-report workflow support.
Clinical Reporting Suite
Diagnostic labs that already generate VCF files; oncology panels; hereditary cancer panels; WES reporting; rare disease workflows; pharmacogenomics reports.
Faster, structured, evidence-linked report generation.
Enterprise Deployment Suite
Larger Diagnostic labs, hospital networks and strategic partners requiring dedicated deployment, APIs, LIMS integration, templates, role-based access, audit logs, workflow configuration, SLA and validation support.
Enterprise-grade genomic intelligence infrastructure.
Clinical Intelligence Extensions
Premium and future capabilities such as molecular tumor board support, clinical trial matching, pharmacogenomics expansion, radiogenomics, multi-omics, biomarker intelligence and cohort analytics.
Extension into higher-value precision medicine workflows.
Validate Seq2Clin with defined samples, workflows, and reporting use cases before full-scale adoption.
Pay per genomic case processed through the Seq2Clin cloud platform.
Commit to annual usage for predictable access, better pricing, and scalable reporting capacity.
Dedicated platform access for organizations needing customization, integrations, and enterprise scalability.
Tailored deployment for partners requiring specialized workflows, private setup, or collaboration.
Seq2Clin is designed to be more than a reporting tool. It brings together bioinformatics workflows, AI-enabled evidence organization, clinical interpretation support, expert review processes, structured report generation, auditability, traceability and enterprise integration readiness.
This makes it a platform for genomic intelligence, not just a software utility.
Let us show how Seq2Clin can support your genomic interpretation and reporting workflow.
Talk to Our Team