Velsera
Provider of cloud-hosted bioinformatics platforms, multi-omic data harmonization, and expert services to support discovery, diagnostic testing, companion-diagnostic development and clinical NGS workflows. Combines secure research environments, data harmonization and standards mapping, graph-based reference-genome methods, variant-interpretation knowledgebases, and professional services (bioinformatics, clinical, regulatory and data teams) with a federated clinical-genomic data network.
Industries
Nr. of Employees
large (251-1000)
Products
Trusted Research Environment (cloud) for bioinformatic analysis and pipeline hosting
Cloud-native environment for running bioinformatic tools and workflows, enabling execution close to data with a tool and workflow catalog and scalable compute.
Pangenotype / graph-based reference-genome and variant-calling tool
Reference-genome tool using graph/pangenotype-based alignment and calling to improve discovery and representation of genetic variation across diverse populations.
Data harmonization and secure sharing platform
Platform to harmonize disparate clinical and genomic data into unified, searchable and shareable datasets for research or commercialization.
Clinical genomics workspace for end-to-end analysis and reporting
Assay- and instrument-agnostic software for run- and case-level QA/QC, interpretation, clinical reporting, therapy-selection support and clinical trial matching.
IVD-grade variant interpretation knowledgebase
Curated clinical variant-interpretation knowledgebase designed to support clinical NGS testing and streamline classification and reporting of clinically significant variants.
Trusted Research Environment (cloud) for bioinformatic analysis and pipeline hosting
Cloud-native environment for running bioinformatic tools and workflows, enabling execution close to data with a tool and workflow catalog and scalable compute.
Pangenotype / graph-based reference-genome and variant-calling tool
Reference-genome tool using graph/pangenotype-based alignment and calling to improve discovery and representation of genetic variation across diverse populations.
Data harmonization and secure sharing platform
Platform to harmonize disparate clinical and genomic data into unified, searchable and shareable datasets for research or commercialization.
Clinical genomics workspace for end-to-end analysis and reporting
Assay- and instrument-agnostic software for run- and case-level QA/QC, interpretation, clinical reporting, therapy-selection support and clinical trial matching.
IVD-grade variant interpretation knowledgebase
Curated clinical variant-interpretation knowledgebase designed to support clinical NGS testing and streamline classification and reporting of clinically significant variants.
Services
Custom pipeline development, workflow automation, cloud migration, GPU-acceleration integration and bioinformatics team augmentation for NGS and multi-omic analyses.
Assessment, ETL ingestion, harmonization and standards mapping to produce research-ready clinical-genomic and multi-omic datasets.
Clinical validation, SOP development, mock audits, on-site go-live support, IT integration, implementation and revenue-cycle management to operationalize clinical NGS testing.
Regulatory strategy, documentation, validation planning, mock audits and IVD-transition support to accelerate regulatory clearance and ongoing compliance.
Study design, program coordination and community engagement to support large-scale translational and research projects.
Custom software and toolchain development, instrument-agnostic implementations and tailored technology components within solution packages.
Custom pipeline development, workflow automation, cloud migration, GPU-acceleration integration and bioinformatics team augmentation for NGS and multi-omic analyses.
Assessment, ETL ingestion, harmonization and standards mapping to produce research-ready clinical-genomic and multi-omic datasets.
Clinical validation, SOP development, mock audits, on-site go-live support, IT integration, implementation and revenue-cycle management to operationalize clinical NGS testing.
Regulatory strategy, documentation, validation planning, mock audits and IVD-transition support to accelerate regulatory clearance and ongoing compliance.
Study design, program coordination and community engagement to support large-scale translational and research projects.
Custom software and toolchain development, instrument-agnostic implementations and tailored technology components within solution packages.
Expertise Areas
- Bioinformatics pipeline development
- NGS assay development and clinical validation
- Multi-omic data harmonization and ETL
- Clinical interpretation, tertiary reporting and decision support
Key Technologies
- Next-generation sequencing (NGS) analysis pipelines
- Cloud-based Trusted Research Environments (TREs)
- Graph-based / pangenotype genome alignment and variant calling
- Multi-omic data ingestion, ETL and harmonization
News & Updates
Commercial partnership to distribute and integrate a clinical genomics workspace in Spain and Portugal with a regional distributor.
Partnership announced with a regional genomics company to advance cancer diagnostics and treatment.
Announcement that GPU-accelerated genomics tools were made available on the hosted analysis platform to accelerate compute-intensive workflows.
Announcement that a clinically curated variant-interpretation knowledgebase supports results reporting for an FDA-cleared oncology IVD.
Release of updated clinical genomics workspace with enhanced variant quality control and clinical evidence review workflows to accelerate analysis and reporting.
Collaboration announced to support integration of imaging and genomics datasets for multimodal research workflows.
Commercial partnership to distribute and integrate a clinical genomics workspace in Spain and Portugal with a regional distributor.
Partnership announced with a regional genomics company to advance cancer diagnostics and treatment.
Announcement that GPU-accelerated genomics tools were made available on the hosted analysis platform to accelerate compute-intensive workflows.
Announcement that a clinically curated variant-interpretation knowledgebase supports results reporting for an FDA-cleared oncology IVD.
Release of updated clinical genomics workspace with enhanced variant quality control and clinical evidence review workflows to accelerate analysis and reporting.
Collaboration announced to support integration of imaging and genomics datasets for multimodal research workflows.