I've been working in a small clinic and we recently encountered a case of a rare genetic disorder that couldn’t be diagnosed using traditional methods. We were really stuck, as we didn’t have a team of bioinformaticians on staff, and the data from the sequencing seemed overwhelming. It felt like we had all this valuable data, but no way to interpret it effectively without the proper expertise. I’ve been wondering if there are any tools or services out there that could help with interpreting NGS data for rare diseases, especially for smaller clinics like ours that can’t afford to hire full-time specialists. Has anyone faced a similar challenge?