42 Genetics
42Genetics is a highly innovative genomics big data company specializing in ultra-fast data processing and analysis solutions for Next Generation Sequencing (NGS) data. Their mission is to provide high-performance, reliable, and scalable genomic analysis tools that support research and clinical applications, including oncology, human genetics, population genetics, agrigenomics, and rare diseases. They aim to accelerate genomic data interpretation, improve accuracy, and facilitate precision medicine and crop improvement through advanced software solutions.
Industries
Nr. of Employees
small (1-50)
42 Genetics
42 Genetics Limited, Concourse Building, Catalyst, Queens Road, BT3 9DT Belfast, Northern Ireland
Products
Modular NGS secondary analysis suite
A modular software suite that ingests raw NGS reads (FASTQ/unaligned BAM), performs high-speed alignment, single-sample and population-based variant calling, somatic calling, and CNV detection; includes a compressed aligned-read file format with conversion tools, programmatic APIs, and a workflow manager.
Modular NGS secondary analysis suite
A modular software suite that ingests raw NGS reads (FASTQ/unaligned BAM), performs high-speed alignment, single-sample and population-based variant calling, somatic calling, and CNV detection; includes a compressed aligned-read file format with conversion tools, programmatic APIs, and a workflow manager.
Services
Deployment and integration of a modular NGS secondary analysis suite into on-premises or cloud environments, including API-based integration with interpretation platforms and data security options.
Services to set up population calling workflows, create cohort-specific profiles, and manage variant repositories for large-scale population or breeding studies.
Configuration and support for tumor/normal somatic calling and copy-number analysis optimized for fast clinical turnaround and cohort-level validation.
Deployment and integration of a modular NGS secondary analysis suite into on-premises or cloud environments, including API-based integration with interpretation platforms and data security options.
Services to set up population calling workflows, create cohort-specific profiles, and manage variant repositories for large-scale population or breeding studies.
Configuration and support for tumor/normal somatic calling and copy-number analysis optimized for fast clinical turnaround and cohort-level validation.
Expertise Areas
- High-throughput NGS data processing
- Clinical and diagnostic genomics (rare disease and oncology)
- Population and agrigenomics cohort analysis
- Bioinformatics pipeline development and optimization
Key Technologies
- Next-generation sequencing (NGS) secondary analysis
- Short-read alignment/mapping
- Single-sample and cohort-based variant calling
- Somatic mutation detection with tumor purity estimation