You asked, and we listened! The Genomenon Team would like to give a big shout-out to all of our users for their constructive feedback on Mastermind and the features that they would like to see incorporated into the software. We have added several new search and display features to address the variant nomenclature issues faced by clinicians, pathologists and geneticists trying to find the most relevant publications on their variant of interest or in designing gene panels.
Our newest variant display features include:
- Genomic coordinate information based on human genome build 37/hg19;
- Reference Sequence accession number of the affected transcript;
- cDNA coordinates for each position in the corresponding codon;
- HGVS-accepted reporting standards to facilitate searching by cDNA or protein-level coordinate systems
We value your feedback, so keep it coming! Additional search and filtering features will be added in the near future, so stay tuned to the Genomenon Blog to keep abreast of our new developments!