BioBox
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BioBox is a data analytics platform for scientists working with next-generation sequencing data.
COMPANY
About Us
LOCATION
88 College St.
Toronto, Canada M5G 1L4
CONTACT
support@biobox.io
2021 BioBox Analytics Inc.
SOLUTIONS
Mutational Analysis
Identify SNVs, SVs and CNVs in a fraction of the time
Mutational Analysis in the BioBox Platform
The BioBox Platform equips scientists with the tools to work with their data seamlessly from start to finish. The user-friendly interface accelerates time to scientific discovery by enabling scientists to conduct rapid analysis in a collaborative suite.
Process
• Build and configure complex pipelines to align, annotate and process your raw data
• Leverage a built-in, interactive GUI to connect workflows (like BWA, Mutect2, Delly and ControlFREEC) without the use of command line
• Run your Mutation Calling pipelines in the cloud
• Generate processed data files (BAM and VCF files) that are automatically saved to your BioBox Library to be used with other powerful features within the platform
Homosapiens
Mus musculus
Analyze
• Create an analysis using your VCF file - either process your FASTQ data in the platform, or use the processed files sent to you by your Bioinformatician
• Use interactive data tables to filter for SNV counts associated with the genes in your analysis
• Auto-generate lollipop plots to visualize point mutations on a per-gene basis
• Annotate mutations with SnpEff
• Identify chromosome position, reference bases and associated alterations of your SNVs
Homosapiens
Mus musculus
Explore
• Search for your gene of interest in the Knowledge Engine and gain access to a plethora of information at the click of a button
• Discover relationships between your gene of interest and your own datasets
• Connect data from multiple public consortiums to your searched gene to explore deeper insights
• Explore gene sets, observations, annotations, gene network maps and disease
Homosapiens
Mus musculus
Comprehensive Features
• Unlimited samples analysis
• Accepts raw data files: BAM and FASTQ
• Accepts processed data files: VCF
• Supports FASTQC, BWA, Mutect2, Delly workflows
• Customizable workflow settings
• Pipeline Design Studio
• Plotting capabilities - bar plots, scatter plots, heatmaps and lollipops
• Interactive plotting capabilities
• Customizable & downloadable plots
• Knowledge Engine
• Preloaded genomic reference data
• SnpEff integration into lollipop plots
Gene Expression
Identify and explore your up- and down-regulated genes.
Knowledge Engine
Search for your gene of interest and return a plethora of information.
Get Started Today.
Pricing Plans