Bioinformatics tools for genotype conversion and VCF processing.
biotec-line provides command-line and desktop tools for working with genetic variant data, from raw DTC DNA files to annotated VCF outputs.
| App | Description |
|---|---|
| VFDistiller | Genetic variant processing with multi-source annotation (gnomAD, Ensembl VEP) |
| genotype-to-vcf | Convert DTC DNA raw data (23andMe, MyHeritage) to VCF 4.2 format |
Related: research-line (open-access research publications)
Part of the ellmos-ai ecosystem.
Desktop app for converting DTC DNA raw data (23andMe, MyHeritage, FTDNA, etc.) to VCF 4.2 format. PyQt6 GUI with auto build detection, dbSNP integration, and dual genome support (GRCh37/GRCh38).
Python 1
Bioinformatic desktop tool for processing, converting, and annotating genetic variant data (VCF, gVCF, 23andMe, FASTA)
Python 1
Desktop app for converting DTC DNA raw data (23andMe, MyHeritage, FTDNA, etc.) to VCF 4.2 format. PyQt6 GUI with auto build detection, dbSNP integration, and dual genome support (GRCh37/GRCh38).
Bioinformatic desktop tool for processing, converting, and annotating genetic variant data (VCF, gVCF, 23andMe, FASTA)
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