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Varsomics

The definitive platform for Geneticists and Bioinformatics

Build to optimize the routine of diagnostic and research laboratories. Easily process and analyze NGS-generated files of human genetic samples. You’re only one click away from the future.

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We are part of the best Hospital in Latin America

We preserve the diversity and the organizational culture of the Albert Einstein Israelite Hospital, considered by America Economia Intelligence’s ranking as the best hospital in Latin America.

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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.

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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 and choice

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.

Institutions that trust our work

Less spreadsheets and manual processing

Varstation® is the ideal solution for analyzing and processing NGS samples. Automate repetitive processes and have more time to dedicate to other important functions of your routine

Main features

VarsACMG®
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®
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.
Varsdata®
Consult frequency data parameterized according
to your analysis and also with the largest databases
in the segment.
VarsSmartFilter®
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.

Explorer®
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.
VarsACMG®
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. varsacmg
Simplify®
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. simplify
Varsdata®
Consult frequency data parameterized according to your analysis and also with the largest databases in the segment. varsdata
VarsSmartFilter®
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. smartfilter
Explorer®
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. smartfilter

Conduct analysis following the College of American Pathologists guidelines.

Varstation® also allows you to implement the main CAP guidelines in your analysis. 

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).

Affordable, on-demand plans

Built-in flexibility to enable rapid changes in the analytical process, affordable pricing, and a powerful, easy-to-use cloud solution. Varstation® was designed to meet your genomics needs.

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