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Frequently Asked Questions
Quick answers about our GPU-accelerated genomics platform
BioInfera is an advanced GPU-accelerated bioinformatics platform that combines cutting-edge AI with cloud-native infrastructure. Our platform leverages NVIDIA Parabricks technology to identify genomic patterns, optimize bioinformatics pipelines, and process sequencing data with clinical-level precision across multiple omics platforms.
We use enterprise-grade encryption and security protocols to protect all genomic and clinical data. All connections are encrypted, and sensitive information is handled according to strict compliance standards.
Our pipelines leverage Python, CUDA, NVIDIA Parabricks, Apache Spark, and Docker to deliver GPU-accelerated, scalable, and reproducible genomics workflows.
We support whole genome sequencing (WGS), whole exome sequencing (WES), RNA-seq (bulk and single-cell), spatial transcriptomics, proteomics, metabolomics, and multi-omics integration from major platforms like Illumina, PacBio, and Oxford Nanopore.
Our platform delivers clinical-grade accuracy (up to 96.7% variant accuracy) and can process over 1TB of sequencing data daily. Whole genome analysis can be completed in under 45 minutes using GPU acceleration.
Yes! We offer extensive customization for pipelines, support for new omics data types, and can adapt workflows to your research needs. Contact us to discuss your requirements.
We provide comprehensive documentation, onboarding, and technical support. Our team is available to assist with setup, troubleshooting, and best practices for genomics research.
Absolutely! BioInfera offers extensive customization options. You can modify pipeline parameters, integrate custom scripts, and adapt workflows to meet your specific research needs. Our team is available to assist with advanced customizations.
BioInfera provides real-time pipeline monitoring through a user-friendly dashboard. You can view detailed logs, performance metrics, resource utilization, and progress updates. Notifications are also available for key pipeline events.
BioInfera supports a wide range of data types including whole genome sequencing (WGS), whole exome sequencing (WES), RNA-seq, single-cell RNA-seq, spatial transcriptomics, proteomics, metabolomics, and multi-omics integration.
BioInfera offers flexible pricing based on your usage and requirements. Costs depend on the volume of data processed, computational resources used, and any additional customizations. Contact us for a detailed pricing plan tailored to your needs.