One of the problems with big data is just that – it's big. There is an almost incomprehensible amount of diverse, non-standardized data that you can use in your ‘omics analyses. You need to invest significant time and resources in finding sources of data and making it usable.
Our team of curators have created a treasure trove of ready-to-use datasets with highly-curated metadata for you to explore and compare.
Discover different worlds of 'omics data that you can compare with and use to validate your own findings. All data is processed, tagged with curated metadata and accessible in slices.
Access thousands of oncology-focused samples, public consortium datasets, single-cell transcriptomic studies and cell line data.
Access thousands of datasets across human diseases and animal models for non-oncology disorders, including single-cell transcriptomic studies and cell line data.
Platform and services for analyzing, visualizing, organizing and unifying your proprietary internal data.
Bioinformaticians and biologists rely on OmicSoft NGS software solutions to facilitate their drug discovery research
Scale your research with secure, hybrid cloud/on-premises options
Deploy in your environment to manage your proprietary 'omics data
Create high-quality, shareable ‘omics analyses
Identify candidate biomarkers for disease or population segments
Find patterns of expression in single cells, tissues, diseases and treatment conditions
Create high-quality, shareable ‘omics analyses
Compare your data to a wealth of 'omics datasets and find novel connections
Access and mine over 700,000 reprocessed ‘omics samples with structured metadata
Process expression data and DNA-seq/SNP arrays through NGS and array analysis workflows
Get in touch with our bioinformatics specialists to see how we can meet your research requirements.
