Customized analyzes from genetic data
- Conduct analysis following College of American Pathologists guidelines.
- Curation of clinically relevant variants with easy interpretation.
- Dynamic and custom filters to create and save pipelines.
Creat an trial account at Varstation®
Main features
Fast and precise identification of variants of impact for your analysis. This feature supports the interpretation of pathogenicity level, pre-classification of variants following the American College of Medical Genetics and Genomics (ACMG) standards.
Simplify building your analytics pipeline. With just a few clicks, choose the optimal parameters to analyze your samples and see all processing settings in real-time.
Consult frequency data parameterized according to your analysis and also with the largest databases in the segment.
Dynamic filters activated with just one click. Designed to ensure targeted and objective analysis of our users' genetic variant lists, this update allows the analyst to create and save custom filtering panels based on pre-established scenarios, with less action time and high performance.
Consult specific parameters from certified databases and many more annotations parameterized according to the American College of Medical Genetics (ACMG) and American Molecular Pathology (AMP) guidelines.Main features
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Fast and precise identification of variants of impact for your analysis. This feature supports the interpretation of pathogenicity level, pre-classification of variants following the American College of Medical Genetics and Genomics (ACMG) standards. |
|
|
Simplify building your analytics pipeline. With just a few clicks, choose the optimal parameters to analyze your samples and see all processing settings in real-time. |
|
|
Consult frequency data parameterized according to your analysis and also with the largest databases in the segment. |
|
|
Dynamic filters activated with just one click. Designed to ensure targeted and objective analysis of our users' genetic variant lists, this update allows the analyst to create and save custom filtering panels based on pre-established scenarios, with less action time and high performance. |
|
|
Consult specific parameters from certified databases and many more annotations parameterized according to the American College of Medical Genetics (ACMG) and American Molecular Pathology (AMP) guidelines. |
How does it work!
Pipeline configuration
Configure and use one of the platform
pipelines informing the platform used to generate the sample file, the library preparation technique and the type of analysis to be performed.
Sample upload and processing
Upload files locally or from Illumina's Basespace. We support the main formats, being them Fastq, BAM, or VCFs.
Curation of clinically relevant variants
The variants are automatically pre-classified by a proper algorithm, and the filter system delimits the variants that may be related to clinical suspicions.
Review and final report
It is possible to review the findings according to the quality recommendations of the accreditation agencies and, after this step, generate a report with the final result of the analysis.
Friendly and intuitive interface
Application developed so that people with different levels of scientific knowledge can perform genetic analysis.
Have more security
Compliance with the most important regulations of quality accreditation organizations such as: CAP and PALC.
Optimize your time
Achieve scalability for your organization through custom pipelines, automatic pre-sorts and more
How does it work!
Pipeline configuration
Configure and use one of the platform pipelines informing the platform used to generate the sample file, the library preparation technique and the type of analysis to be performed.
Sample upload and processing
Upload files locally or from Illumina's Basespace. We support the main formats, being them Fastq, BAM, or VCFs.
Curation of clinically relevant variants
The variants are automatically pre-classified by a proper algorithm, and the filter system delimits the variants that may be related to clinical suspicions.
Review and final report
It is possible to review the findings according to the quality recommendations of the accreditation agencies and, after this step, generate a report with the final result of the analysis.
Friendly and intuitive interface
Application developed so that people with different levels of scientific knowledge can perform genetic analysis.
Have more security
Compliance with the most important regulations of quality accreditation organizations such as: CAP and PALC.
Optimize your time
Achieve scalability for your organization through custom pipelines, automatic pre-sorts and more.
We are part of the best Hospital in Latin America:We preserve the diversity, quality and organizational culture of Hospital Israelita Albert Einstein, considered by the América Economía Intelligence ranking as the best hospital in Latin America. |
Rare Genomes Project - BrazilBy sequencing thousands of patients, the project will allow the creation of the largest Brazilian genetic bank of patients with rare diseases and hereditary cancer risk, through the Unified Health System (SUS). |
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We are part of the best Hospital in Latin America:We preserve the diversity, quality and organizational culture of Hospital Israelita Albert Einstein, considered by the América Economía Intelligence ranking as the best hospital in Latin America. |
Rare Genomes Project - BrazilBy sequencing thousands of patients, the project will allow the creation of the largest Brazilian genetic bank of patients with rare diseases and hereditary cancer risk, through the Unified Health System (SUS). |
Advantages of using Varstation®
Optimization of the time of analysis
Significantly reduce and optimize the time for processing, sorting variants and generating reports from NGS (Next Generation Sequencing) human genetic samples.
End-to-end automated processing
Quality parameter evaluation, mapping, multi-variant callers, database annotation, and automatic pre-sorting following ACMG, AMP, PALC, and CAP guidelines.
Support for clinical interpretation
More than 200 databases of genetic variants are incorporated, including data for germline and somatic analyses.
Robust filters
The filtering mechanism incorporates all annotated mutation data - including human phenotypes, patient clinical history and diseases (OMIM/UniProt).
Trusted by
Sucess Case
During the COVID-19 pandemic, Varsomics, in partnership with Hospital Israelita Albert Einstein, developed the world’s first test for the diagnosis of the new coronavirus based on Next Generation Sequencing (NGS). The test, which was known as VarsVid, identifies the presence of the virus, functioning as a diagnostic tool to be used from the first day of infection, in the same way as RT-PCR, which makes it an alternative for adopting a diagnostic test. Processing takes up to 72 hours, and has 95% sensitivity and 99% specificity, or positive, there are no cases of false.
By as you go, or grow
Flexibility to enable fast changes to the analytics process, affordable pricing, and a powerful, pay-as-you-go cloud solution.
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