Search life sciences software.

by QIAGEN

Comprehensive database of 220,000+ published human inherited disease mutations with advanced search, visualization, and genome browser integration for clinical and research use.

by QIAGEN

NGS analysis, interpretation, and reporting for precision oncology, from FASTQ to final clinical report.

by QIAGEN

AI-enabled variant interpretation and NGS analysis for hereditary disease diagnosis, from FASTQ to final clinical report.

by Magna Labs

QA automation and validation for bioinformatic pipelines, software, and omics data with no-code setup.

by Pythia Biosciences

Integrated analysis and visualization of multi-omics data across genomics, transcriptomics, proteomics, metabolomics, and more.

by Pythia Biosciences

Standardized multi-omics database with interactive access to 10,000+ harmonized datasets across RNA-seq, proteomics, and spatial transcriptomics.

by Pythia Biosciences

Programmatic access to a curated multi-omics database of 10,000+ datasets for Jupyter Notebook and RStudio environments.

by DeepChain

Generative DNA models for single-nucleotide resolution genomic insights, molecular phenotype prediction, and element segmentation across species.

by Tempus

Secure portal for ordering genomic tests, tracking order status, and viewing comprehensive patient results with AI-assisted clinical insights.

by Tempus

AI-driven oncology tests for immune response, homologous recombination deficiency, tumor origin, and drug metabolism prediction.

by SOPHiA GENETICS

Analysis, standardization, and interpretation of genomic, radiomic, and multimodal healthcare data with AI-powered variant detection and image segmentation.

by SOPHiA GENETICS

Genomic variant detection and interpretation for oncology and rare disorders using AI-powered analysis of NGS data.

by SOPHiA GENETICS

Variant visualization and annotation for genomic interpretation, with ACMG classification and integrated prediction tools.

by SOPHiA GENETICS

Contextualize genomic cancer biomarkers and track them longitudinally for confident precision oncology decision-making.

by Seven Bridges

Cloud-based biomedical data analysis and collaboration for genomics research at scale, with reproducible workflows and multi-cloud infrastructure.

by Seven Bridges

Genomic and phenotypic analysis at million-participant scale with data exploration, variant annotation, and statistical workflows.

by Seven Bridges

Graph-based variant calling and alignment for NGS data using pan-genome references that capture population-specific genetic diversity.

by Seven Bridges

Automation script development and execution for genomics workflows with Python, CLI, API, and visual interfaces.

by Genomoncology

Unified data infrastructure and AI-driven analytics for precision oncology programs, from molecular pathology to clinical trial matching.

by Genomoncology

NGS workflow automation from data ingestion to compliant clinical genomic report delivery with variant interpretation and EHR integration.