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.
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.
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.
Upload files locally or from Illumina's Basespace. We support the main formats, being them Fastq, BAM, or VCFs.
The variants are automatically pre-classified by a proper algorithm, and the filter system delimits the variants that may be related to clinical suspicions.
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.
Application developed so that people with different levels of scientific knowledge can perform genetic analysis.
Compliance with the most important regulations of quality accreditation organizations such as: CAP and PALC.
Achieve scalability for your organization through custom pipelines, automatic pre-sorts and more
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
Upload files locally or from Illumina's Basespace. We support the main formats, being them Fastq, BAM, or VCFs.
The variants are automatically pre-classified by a proper algorithm, and the filter system delimits the variants that may be related to clinical suspicions.
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.
Application developed so that people with different levels of scientific knowledge can perform genetic analysis.
Compliance with the most important regulations of quality accreditation organizations such as: CAP and PALC.
Achieve scalability for your organization through custom pipelines, automatic pre-sorts and more.
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
Varstation® also allows you to implement the main CAP guidelines in your analysis.
Significantly reduce and optimize the time for processing, sorting variants and generating reports from NGS (Next Generation Sequencing) human genetic samples.
Quality parameter evaluation, mapping, multi-variant callers, database annotation, and automatic pre-sorting following ACMG, AMP, PALC, and CAP guidelines.
More than 200 databases of genetic variants are incorporated, including data for germline and somatic analyses.
The filtering mechanism incorporates all annotated mutation data - including human phenotypes, patient clinical history and diseases (OMIM/UniProt).
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.