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Chanjo provides a better way to analyze coverage data in clinical sequencing.

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Fetch it dynamically from `store.engine.url`

Hi Robin, The demo was failing because the chromosome names didn't match up with the alignment files. This fixes that. Hope you are well.

Since we are touching the code again, let's!

I tried to make a custumized coverage report for a gene (NR2E2, HGNC ID 7974) I get a 0/0 transcripts ,see image ![image](https://github.com/user-attachments/assets/1198f716-bd9f-405e-9c8e-8691d9e53caa) ad the gene is present in the...