Seq Smart

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SeqSMARTwhere genomics meets the future
AI-driven genomic insight enhacment platform
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Speeding up data

interpretation

Improved classification by AI

Comprehensive Genomic Solutions
A wide range of genomic analysis services is offered at SeqSMART, from targeted gene studies to full genome sequencing,tailored for both professionals and individuals seeking insights into their DNA
Pathogenic Variant Identification

We prioritize clinically significant variants using a multi-tiered approach, blending industry standards, innovation, and expert insights.

Pedigree Drawing & Data Analysis

Create pedigrees, gather clinical data, and use AI-powered analysis to uncover genetic patterns for informed decisions.

The SeqSMART Advantage

SeqSMART combines AI, expert insights, and comprehensive tools to deliver precise genomic data for confident decision-making.

Quality and Data Integrity

Access detailed quality metrics to ensure reliable genomic data and make informed decisions with full coverage insights.

Comprehensive Genomic Testing

SeqSMART offers Sanger sequencing, gene panels, WES, WGS, and somatic variant analysis for precise genomic insights.

Trusted Expert Team

Rely on our team of genomic, bioinformatics, and clinical genetics experts for high-quality analyses and interpretations.

Precise CNV Analysis

Detect and explore CNVs from single exons to large chromosomal regions with SeqSMART's advanced technology.

In-House Patient Variant Database

Compare new cases with previously analyzed variants for enhanced diagnostic accuracy and efficient research cross-referencing.

Fast and Accurate Data Processing

Receive rapid data interpretation in under 5 minutes without compromising quality, ensuring timely results for clinical and research needs.

Constantly Updated Data

SeqSMART ensures access to the latest information from trusted genomic databases, keeping your analyses relevant and cutting-edge.

Affordable Genomic Analysis

SeqSMART provides competitive pricing for high-quality genomic services, making them accessible to clinicians and researchers alike.

Explore Your DNA Easily

SeqSMART offers a user-friendly service for individuals to discover their genetic makeup through a simple buccal sample analysis.

Advanced Variant Identification and Classification

At SeqSMART, clinically significant variants are prioritized using a multi-tiered approach for accurate pathogenicity determination. Our platform integrates ACMG/AMP 2015 guidelines with ClinGen recommendations, an AI-powered reinforcement learning engine, and a community-driven classification model. This comprehensive framework ensures precise variant interpretation, leveraging expert collaboration to address complex classifications and continually enhance our understanding of pathogenicity.

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Features and Specifications

SeqSMART’s Unique Features

  • Advanced Pedigree and Clinical Data Tools

  • Customizable Analysis Pipelines

  • Multiple Data Format Support

  • User-Controlled Workflow

  • User-Friendly Interface

  • Patient History Access

  • Autopilot Mode

Key Features

  • Comprehensive CNV Detection & Filtering

  • Comprehensive Quality Control Metrics

  • Flexible Variant Classification

  • Integrated Data Visualization

  • AI-Driven Variant Ranking

  • Instant Report Creation

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