We’d like to make you aware of two bioinformatics positions open at Boston Children’s Hospital, in support of pediatric rare diseases including early onset epilepsy, very early onset inflammatory bowel disease and ultra-rare orphan diseases. The first position(https://sjobs.brassring.com/TGnewUI/Search/Home/Home?partnerid=368&siteid=5205#jobDetails=3070873_5205) is focused on integrating and analyzing host and viral genomics, transcriptomics, phenotypes and lab measurements from pediatric patients with severe COVID-19 requiring hospitalization. The second position (https://sjobs.brassring.com/TGnewUI/Search/Home/Home?partnerid=368&siteid=5205#jobDetails=3080576_5205) is for a senior bioinformatics scientist, who will be collaborating with leading pediatric researchers from across the institution and supporting wide ranging analysis including genomic, transcriptomic, epigenomic, and proteomic analyses to identify novel biological insights. Both positions offer growth opportunities to trainees with a strong background, experience with next generation sequencing data and a strong publication record. If you know of any candidates in your department that might fit one of these positions, please let us know or post this in your forums. To learn more about our rare disease cohort initiative please refer to our recent npj Genomic Medicine manuscript.