New in emedgene 2.23 (Jun 15, 2021)
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With gnomAD no longer releasing GRCh37 versions, we expect increased lab transitions to GRCh38. We have incorporated the two most requested GRCh38 features in this release, thus offering you complete support for GRCh38:
A totally unified workflow for tests running on different reference genomes in the same organization.
A solution for historical data. Curated and historical data are automatically lifted over on the fly and made available as you perform your analysis (in either reference).
The Cases tab has a brand new design, but more importantly - a new feature set:
grouping cases by Case Status,
refined case filtering,
effortless customization of the Cases table view,
and more!
