CZ CELLxGENE Discover
Select two custom cell groups based on metadata to find their top differentially expressed genes. Leverage millions of cells from the integrated CZ CELLxGENE corpus for powerful analysis. Execute interactive analyses on a dataset to explore how patterns of gene expression are determined by spatial, environmental, and genetic factors using an interactive speed no-code UI. Understand published datasets or use them as a launchpad to identify new cell sub-types and states. Census provides access to any custom slice of standardized cell data available on CZ CELLxGENE Discover in R and Python. Explore an interactive encyclopedia of 700+ cell types that provides detailed definitions, marker genes, lineage, and relevant datasets in one place. Browse and download hundreds of standardized data collections and 1,000+ datasets characterizing the functionality of healthy mouse and human tissues.
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SnapGene
Accurately design and simulate cloning procedures. Test complicated projects, catch errors before they happen, and obtain the right constructs the first time. Cloning is easier when you can see what you are doing. The intuitive interface offers you unparalleled visibility into your work, simplifying often complex tasks. SnapGene automates documentation, so you don’t have to. See and share every sequence edit and cloning procedure that led to your final plasmid. Improve your core molecular biology procedures, and improve your results. Master SnapGene and key concepts in cloning with our new online learning center, SnapGene Academy. Containing over 50 video tutorials taught by scientific experts, SnapGene Academy helps you advance your skills across multiple molecular biology courses. SnapGene 7.2 provides a new visualization of primer homodimer structures and enhancements to file management, allowing tabs to be organized in multiple windows using drag and drop.
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Folklore Clinical Variant Interpretation
Folklore is Helena Bioinformatics’ flagship clinical variant interpretation platform for genomics laboratories. It combines VCF analysis, curated evidence, literature, phenotype, inheritance and prioritisation in a traceable specialist workflow. Panels, exomes and genomes include nuclear, mitochondrial and structural/copy-number variants with ACMG/AMP, MMDWG and Riggs frameworks.
Its separate public, read-only Folklore MCP 1.6.0 offers 11 tools for public GRCh38 germline variant evidence, literature, ClinGen gene-disease associations and optional support. New resolve_gene, get_gene_profile, get_gene_section and search_gene_literature add explicit gene selection, snapshot-pinned profiles and sections, and separate live gene literature. MCP uses Streamable HTTP without an account or API key; it accepts no patient data, VCF uploads or batch analysis.
Results support qualified professional review and are not diagnoses or treatment recommendations.
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ProcessGene BPM Software
ProcessGene is the leading provider of software solutions for Business Process Management (BPM). The BPM software solutions are implemented within days, immediately creating visibility and centralized control. Businesses and governments worldwide use the ProcessGene™ BPM software cloud to manage, control and improve business processes, implement enterprise software, and coordinate mergers and acquisitions. ProcessGene™‘s BPM software is designed for multi-subsidiary organizations, based on our Multi-Org technology. ProcessGene™ has been a pioneer and global leader in Multi-Org BPM technology. During the past decade we have mastered a unique expertise in providing software solutions to multi-subsidiary organizations worldwide. Our BPM software cloud has been specifically designed for multi-subsidiary organizations and it features the most comprehensive solution for complex, distributed business process planning, improvement, and implementation challenges.
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