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Manual
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
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VarSome Help Center
Manual
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
Manual
Step-by-step instructions for VarSome Clinical and description of all its features.
What is VarSome Picks?
Publications related to variants
Introduction
Two Factor Authentication
Launch an analysis (without workflows)
VarSome Clinical Group Supervisor
Sample Management
Data Upload
Sample tags
Illumina BaseSpace Integration
Analyses
CNV/SV analysis sensitive mode
CNV/SV annotation (from VCF)
VarSome Clinical Tokens management
Accepted input files
Requirements for submitted VCF files
Launching sub-analyses
Merging analyses
Custom transcript for annotation
CNV/SV calling analysis
Repeat expansion annotation from VCF file
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Results
Analyses' tabs
How can I inspect my analysis results on more than one monitors?
Dashboard
Variant table
Analysis Actions menu
Custom Variant Classifications
Import of classifications and comments
Sample cross-referencing
Phenotype Matching
CNV visualization
Sample View
What is VarSome Clinical PGx?
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Filters
Dynamic filters
Gene lists
Segregating variants analysis
Reporting
Variant Selection
Report Generation
Report files to download
Coverage report for targeted regions
Region list coverage report
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Quality Control
User Messages - FASTQ and alignment QC
Quality Control Report
FastQC Report
Audit Trail
Legal
ISO 13485 Certificate
CE-IVD Declaration of conformity
HIPAA Compliance Statement
Hébergeur de Données de Santé (HDS)
ISO 27001 Certificate
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