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Genetase provides manual reanalysis of direct-to-consumer genomic data, including whole genome sequencing (WGS), whole exome sequencing (WES), and raw VCF files from providers such as Nebula Genomics, Dante Labs, Veritas Genetics, Sequencing.com, TellmeGen, and others. We specialise in expert-led interpretation of existing genomic data, including variant interpretation, rare variant discovery, and structured reanalysis beyond standard automated consumer reports. Each dataset is manually reviewed by a PhD-trained scientist using multi-database annotation pipelines and research-grade interpretation methods. Our service is designed for users who already have raw genomic data from consumer sequencing providers and want a deeper, independent reanalysis of their results, including investigation of rare and potentially novel variants, as well as targeted research questions. We also provide bioinformatics consulting for academic labs, biotech, and pharma organisations, including VCF annotation and variant prioritisation consulting, bioinformatics pipeline design and optimisation, custom genomic database development, cohort analysis support, and research-focused genomic data interpretation for research projects.
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United Kingdom
- genetase.com
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