I’ve never personally dealt with NGS data, but I’ve read a lot about how crucial it is in diagnosing rare conditions. From what I understand, being able to interpret such data quickly can really change the way these diseases are diagnosed, especially when resources are limited. It seems like advancements in genetic analysis tools are making it more accessible for smaller labs and clinics. If you're looking to dive into this field, I'd recommend looking into software that focuses specifically on healthcare applications – sometimes they provide more tailored solutions for small teams.