All FAQ

"Failed to generate report". What should I do?How do I check the version of my environment?How do I move between organizations?What is the required format for a BED file defining a kit?How does joint calling work on Emedgene?Can I use exome data for CNV detection?How do I prepare VCF files generated by DRAGEN MANTA to be used as input for Emedgene?How do I prepare VCF files generated by Dragen STR (ExpansionHunter) to be used as input?How do I analyze mtDNA variants?Which browser should I use with Emedgene?How do I use developer tools to collect logs?Can I analyze Illumina Complete Long Reads in Emedgene?Source of gnomAD data for small variants on GRCh38How are MNVs handled on the platform?Support for gene lists with up to 10,000 genesGenomic Regions by Case Typehttps://github.com/illumina-swi/emedgene-docs/blob/prod/frequently-asked-questions/all-faq/how-does-emedgene-analyze-prioritize-transcripts.mdhttps://github.com/illumina-swi/emedgene-docs/blob/prod/frequently-asked-questions/all-faq/performance-issue-troubleshooting.md

Variant Effect Filters