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Description

SeqOne is an advanced genomic analysis platform powered by artificial intelligence, aimed at enabling molecular laboratories, clinical teams, biologists, and geneticists to convert intricate next-generation sequencing data into quick, accurate, and actionable clinical insights that aid in personalized medicine diagnostics. By streamlining the entire genomic workflow—from handling raw sequencing data to variant interpretation and reporting—this platform automates routine tasks, integrates smoothly with laboratory systems, and employs sophisticated AI models like DiagAI to assess and prioritize disease-related variants, thereby minimizing manual labor and shortening turnaround times. SeqOne is versatile, catering to both germline and somatic analyses across various fields such as oncology, rare inherited diseases, and infectious disease detection, while it combines high-quality annotation databases and standardized interpretation protocols to ensure clinical-grade precision. Furthermore, it features an intuitive user interface that can scale securely through the cloud, making it accessible and efficient for diverse clinical environments. Ultimately, SeqOne represents a significant advancement in genomic analysis technology, fostering enhanced diagnostic capabilities in the realm of personalized medicine.

Description

VSClinical facilitates the clinical analysis of genetic variants in accordance with ACMG and AMP guidelines. Its structured workflow supports adherence to the American College of Medical Genetics (ACMG) standards, which are essential for identifying and categorizing pathogenic variants related to inherited disease risk, cancer susceptibility, and rare disease diagnosis. The combined ACMG/AMP guidelines for variant interpretation establish a framework for scoring variants and categorizing them into one of five classification levels. Implementing these guidelines necessitates a thorough examination of annotations, genomic contexts, and pre-existing clinical insights for each variant. VSClinical streamlines this process by offering a customized workflow that evaluates each relevant criterion and supplies comprehensive bioinformatics, literature references, and clinical knowledgebase evidence to aid in the scoring and interpretation of variants. This innovative approach is designed to enhance the efficiency of variant scientists as they navigate the complexities of variant processing and analysis. Overall, VSClinical stands out as a vital tool for accelerating the understanding and classification of genetic variants in clinical settings.

API Access

Has API Yes 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

GenomeBrowse No 
VarSeq No 

Integrations

GenomeBrowse Yes 
VarSeq Yes 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

No price information available.
Free Trial Yes 
Free Version No 

Deployment

Web-Based Yes 
On-Premises Yes 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours No 
Live Rep (24/7) No 
Online Support Yes 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Types of Training

Training Docs Yes 
Webinars No 
Live Training (Online) No 
In Person No 

Types of Training

Training Docs Yes 
Webinars Yes 
Live Training (Online) Yes 
In Person Yes 

Vendor Details

Company Name

SeqOne

Founded

2017

Country

France

Website

www.seqone.com

Vendor Details

Company Name

Golden Helix

Founded

1998

Country

United States

Website

www.goldenhelix.com/products/VarSeq/vsclinical.html

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