VarSeq
Simple, fast, and repeatable variant analysis software for gene panels, exomes, and whole genomes. VarSeq is an intuitive, integrated software solution for tertiary analysis. With VarSeq you can automate your workflows and analyze variants for gene panels, exomes, and whole genomes. Understanding genomic data has never been easier thanks to our software. VarSeq software provides a powerful filtering and annotation engine to sift through large variant data sets. Using a chain of filters, you can quickly narrow your list of variants down to those that are most likely to be of interest. After determining the parameters that work well for your analysis, you can save the state of your filters so that you can easily apply the same analysis to another dataset. The same automated workflow can be used for each batch of samples, making VarSeq an ideal solution for high-throughput environments. Real-time filtering gives you the power to quickly prototype and tune analysis workflows.
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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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Geneious
Geneious Prime makes bioinformatics accessible by transforming raw data into visualizations that make sequence analysis intuitive and user-friendly. Simple sequence assembly and easy editing of contigs. Automatic annotation for gene prediction, motifs, translation, and variant calling. Genotype microsatellite traces with automated ladder fitting and peak calling and generates tables of alleles. Beautiful visualizations of annotated genomes and assemblies are displayed in a highly customizable sequence view. Powerful SNP variants analysis, simple RNA-Seq expression analysis, and amplicon metagenomics. Design and test PCR and sequencing primers and create your own searchable primer database.
Geneious Biologics is a flexible, scalable, and secure way to streamline your antibody analysis workflows, create high-quality libraries and select the optimal therapeutic candidates.
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Conspecta
Conspecta is a browser-based platform for life science research. Image analysis, flow cytometry, molecular biology, sample tracking, and publication-ready figures all live in one connected workspace. Each result is linked to where it came from, so any number traces back to its sample, images, and analysis in one click. Image analysis pipelines count cells and colonies and measure area and intensity. Flow cytometry covers gating, compensation, UMAP, and clustering, with FlowJo and Gating-ML import and export. Inventory, orders, freezer maps, instrument booking, protocols, a lab notebook, and live project reports sit in the same workspace. Labs connect Claude, ChatGPT, or Copilot over MCP, and their own scripts through the REST API. Records import from CSV, Excel, and Word, so a lab can move over while its current system keeps running. Free for one scientist and one collaborator, and paid plans open it to a whole lab.
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