Existing data analysis solutions for genomics are laborious, time-consuming and incomplete. You have to manage various systems, navigate complex workflows and spend inordinate amounts of time hunting for annotations and creating data visualizations. Good news: those days are over. VIA software radically simplifies your sample-to-report workflow and empowers you to deliver more clinically relevant answers from across technologies faster. VIA brings various data types into one view and automates variant calling, interpretation and annotation, so you can reduce turnaround times and optimize operations at every step.
VIA software amplifies the story of your data by automatically generating powerful visualizations for enhanced variant contextualization across multiple variant types happening in the same genomic region.
VIA allows you to drill down to single chromosome, gene, and nucleotide levels for deeper analysis. Leverage multiple views, including genome browser, karyogram, track view, and circos plot.
VIA software introduces intelligent automation for filtering, classifying, annotating and interpreting data across technologies, no more hours manually searching through databases.
VIA accelerates time to results to drive faster, informed interpretations while reducing associated costs.
Easily create reports communicating results with simplicity and clarity thanks to VIA’s customizable reporting options. Bring the most relevant information to the surface along with visuals and data that support decision-making that meet guideline-based requirements.
VIA also provides the option for utilizing the new hematological malignancy workflow for a streamlined analysis and reporting solution for OGM data. See the Application Spotlight.
VIA eliminates complex data analysis workflows by bringing data types together in one centralized platform, including your historical data from previous cases. You can seamlessly transition between technologies and all classes of genomic variation within VIA software.
The latest versions of Bionano Solve, Bionano Access™, and VIA software combine to deliver a comprehensive and automated workflow for analyzing, interpreting, and reporting SVs and CNVs detected by OGM associated with hematological malignancies.
This complete workflow leverages intelligent software automation to reduce the time to result for hematological malignancy sample data from OGM, including curated resources in VIA software that represent guideline-based targets applicable to hematological disease. VIA software automatically pre-classifies variants detected with OGM according to a rules-based engine to classify events based on pathogenicity or variant tiering system.
These oncology workflows are configurable to your site-specific preferences.
|Genome Browser Visualization||✓||✓||✓|
|Circos Plot Visualization||✓||✓|
|OGM Molecule Maps||(links to Access)||✓|
|SNP-FASST3 CNV & AOH||✓|
|B-Allele Frequency Plot for OGM||✓|
|Integrated HRD Scar Analysis||✓||✓|
|T2T Human Genome Compatibility||✓||✓|
|Interpretation and Reporting|
|Automated Variant Classification||✓||✓|
|Robust Gene/Variant Annotations||✓||✓|
|Local Variant Database||✓||✓|
|Connection to MasterMind||✓|
|ACMG-based CNV Scoring||✓||✓|
|Dynamic Variant Filtering||✓||✓||✓|
|Heme Guideline Analysis||✓|
|Configurable Report Generation||✓|
|OGM Data Compatibility||✓||✓|
|NGS & Array Data Integrations||✓||✓|
|Structural Variant Analysis||✓||✓|
|Sequence Variant Analysis||✓||✓|
Watch a short video explaing how VIA worksWatch Video
Read more about homologous recombination deficiency and how Bionano VlA software provides in-depth analysis of HRDRead White Paper
Learn more about the value of integrating multiple datasets. Download a list of recent publications where OGM was combined with NGS to investigate disease cases.Download Summary
See How the Software Works
Talk to a specialist to discuss how you can benefit from VIA in more detail or request a demo to review the software to see how it can detect and analyze genome-wide variation.