The following article for this Special Issue was previously published and can be found in their respective issues or online. Issue 9 (25th January 2020) - Unknown
Abstract : Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype‐weighted knowledge in the CAGI SickKids5 clinical genomes challenge (41: 2) https://onlinelibrary.wiley.com/doi/10.1002/humu.23933