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
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.
42Genetics NGS Secondary Analysis Solution
A modular high performance NGS secondary analysis solution that provides reliable bridging from NGS data streaming to detailed genetic interpretation and reporting solutions.
42Genetics Map
The cornerstone for NGS data analysis using a patented high performance mapping algorithm, creating a GAR file with high size reduction.
Human Genetics NGS Analysis Solution
Whole Genome Sequencing analysis solution providing predictable service levels from 20 minutes per full genome processing to 1 hour for full genome trio analysis with high sensitivity variant calling.
42Genetics CNV
Computes a normalized differential between two inputs or a sample and a group of samples for copy number variation detection.
42Genetics Variant Calling Technology
Patented variant calling technology at the heart of germline, somatic, trio, and population calling.
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.
42Genetics NGS Secondary Analysis Solution
A modular high performance NGS secondary analysis solution that provides reliable bridging from NGS data streaming to detailed genetic interpretation and reporting solutions.
42Genetics Map
The cornerstone for NGS data analysis using a patented high performance mapping algorithm, creating a GAR file with high size reduction.
Human Genetics NGS Analysis Solution
Whole Genome Sequencing analysis solution providing predictable service levels from 20 minutes per full genome processing to 1 hour for full genome trio analysis with high sensitivity variant calling.
42Genetics CNV
Computes a normalized differential between two inputs or a sample and a group of samples for copy number variation detection.
42Genetics Variant Calling Technology
Patented variant calling technology at the heart of germline, somatic, trio, and population calling.
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