I totally get what you're saying. It can be overwhelming when you’re dealing with complex data like NGS without the right expertise. I had a similar experience with a project last year. We didn't have bioinformaticians on hand, so we turned to external solutions. I found that services like https://compassbioinfo.com/ offer platforms that simplify the interpretation of genetic data. They have tools specifically designed for handling complex cases, including rare genetic diseases, and they can really save time and resources. For us, it made a huge difference in how quickly we could start diagnosing and offering the right treatments. You might want to check them out if you haven’t yet!