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VarSome Help Center
FAQ
Manual
Sample Management
Analyses
Results
Filters
Reporting
Quality Control
Legal
Germline Variant Classification
General
Variant Interpretation
FAQ
General
User Interface
Pipelines
In silico algorithms
Troubleshooting
Pricing and billing
For Partners
VarSome API
ClinVar
Features
FAQ
Answers for frequently asked questions from users and clients.
CNV Quality Control: tools and guidelines
How could a common variant be classified as pathogenic?
What are the different ways to activate 2 Factor Authentication?
I do not receive the SMS code for the Two Factor Authentication. What happened?
General
Why is the variant annotation different on VarSome and VarSome Clinical?
How does VarSome's throttling work?
How can I link a publication to a variant?
Mitochondrial genome versions
How can I access the premium resources offered by VarSome Premium?
What are the requirements for the trial period of VarSome Clinical?
Variant Sharing Program
Phasing
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User Interface
Adding an assay to VarSome Clinical
How can I quickly check the coverage for a specific exon of a given transcript or gene?
How can I apply algorithmic filters on my analysis?
Downloading variant annotation data
Assay missing in the list
Why do the clinical cards not change when I select one variant?
How can I launch an analysis of several independent samples?
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Pipelines
Targeted/Untargeted Calling on VarSome Clinical
Splicing variants
Validation of VCF files
iSeq Adapter Trimming
Agilent OneSeq
Alignment and Calling
How are the variants identified?
How are pipelines validated?
Which reference genome is being used to align the reads?
How can I validate my laboratory pipeline and bioinformatics results?
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In silico algorithms
Is CADD available in the VarSome suite?
What is the meaning of the MutationTaster Score and the MutationTaster Predictions?
Troubleshooting
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