All FAQ

Emedgene annotations and update frequencyHow do I check my platform version?How do I move between organizations?Required format for a BED file defining a kitJoint calling in EmedgeneCan I use exome data for CNV detection?Formatting DRAGEN MANTA VCFs for EmedgeneFormatting DRAGEN STR VCF files for EmedgeneHow 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 GRCh38Processing multi-nucleotide variantsSupport for gene lists with up to 10,000 genesPerformance issues troubleshootingTranscript prioritization logicVariant effect and severity calculationVariant effect filters