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VarSome Clinical FAQs

1. 3D protein viewer


2. ClinVar


3. Explanation of VCF attributes


4. How can I filter out artifacts from my samples?


5. Why are variants identified in a single strand considered as artifacts, in particular when using amplicon kits?


6. Pseudogenes


7. Variant Sorting


8. Tumor Mutational Burden (TMB)


9. Variant not found


10. Investigating exon coverage


11. Publications Timeline Visualization


12. Joint calling


13. Variant calling and quality filters


13.1. Variant calling local reassembly


14. CNVs


15. Why does the position of some indels reported not match the position of the indels reported by ExAC/Gnomad?


16. Filter by Frequency or Pathogenicity


17. Hemizygous Variants


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