Gencove Methodologies
- What is Effective Coverage?
- What program is used for genotype imputation?
- How do you impute genotypes when there are no reads at a site?
- How do you calculate contamination for a sample?
- Can I get access to the variants called directly from the BAMs before imputation?
- What does the LOWCONF filter mean for a variant?
- Can you share any open-source bioinformatics tools in your production pipelines?
- What tool is used for CNV calling?