Helena Bioinformatics

Evidence presents versioned scientific studies with methods, results, sensitivity analyses and source files. It helps biomedical researchers examine how a reported result was produced and follow the evidence behind it. Readers can inspect the released study materials and their provenance.Developed by Helena Bioinformatics in Sofia, Bulgaria. Evidence is a separate product alongside Folklore, our flagship genomic interpretation product, Noodle biomedical literature discovery and Undertone GWAS analysis.Product: https://evidence.helena.bio/Company: https://www.helena.bio/Contact: contact@helena.bio

Noodle helps biomedical researchers discover publications and explore how scientific evidence connects. Search by meaning, inspect papers and follow citation and semantic relationships to find relevant research beyond an isolated keyword result.Built by Helena Bioinformatics in Sofia, Bulgaria, Noodle complements Folklore Clinical Variant Interpretation within our connected software ecosystem. It supports literature exploration and evidence review for laboratories, universities and research teams. Researchers remain responsible for evaluating source publications and their relevance.Explore Noodle: https://noodle.helena.bioContact: contact@helena.bioCompany: https://www.helena.bio/

Undertone helps genetics and biomedical research teams analyse a complete genome-wide association study. It brings ranked loci, fine-mapping, candidate genes, tissues and testable mechanism hypotheses into a whole-study research workflow. Candidate mechanisms remain hypotheses for further investigation.Developed by Helena Bioinformatics in Sofia, Bulgaria. Undertone complements Folklore, our flagship genomic interpretation product, alongside Noodle biomedical literature discovery and Evidence versioned scientific studies.Product: https://undertone.helena.bio/Company: https://www.helena.bio/Contact: contact@helena.bio

Folklore, the flagship product of Helena Bioinformatics, helps genetics laboratories review variants from panel, exome and genome VCFs. It brings ACMG/AMP classification, phenotype, inheritance and literature evidence into one workflow for variant prioritisation and professional interpretation. Qualified specialists review the evidence and final interpretation.Developed by Helena Bioinformatics in Sofia, Bulgaria. Contact us to discuss a demonstration or your laboratory workflow.Product: https://folklore.helena.bioDemonstration: https://www.youtube.com/watch?v=stHBv2gJYz4Research Use Only. Not CE-marked. Outputs require qualified professional review and do not constitute an autonomous diagnosis.Company: https://www.helena.bio/