Welcome to CGAR’s documentation!¶
- 1. Introduction
- 2. Upload Own Variant Files
- 3. Start Analysis on CGAR
- 4. Inside CGAR Report
- 4.1. Genotype-based prediction of ancestral composition
- 4.2. Side menu and main table
- 4.3. HGMD variants
- 4.4. ClinVar variants
- 4.5. Genes associated with rare phenotype
- 4.6. Putative phenotype-associated genes
- 4.7. Secondary findings
- 4.8. Pharmacogenomic variants
- 4.9. User-defined set of genes
- 4.10. De novo variant candidates
- 4.11. Cancer-associated genes and variants
- 5. Running CGAR locally
- 6. Contact