OFC-SV: Interpreting structural variants in African and Asian cohorts with non-syndromic orofacial clefts
OFC-SV is a web-based data portal designed to help interpret structural variants (SVs) in non-syndromic orofacial clefts genomic data published by The Gabriella Miller Kids First Pediatric Research Program. The portal offers a user-friendly way to explore 41 novel SV genes (of these 13 sharing regulatory perturbations already reported in the literature as SNV genes) potentially responsible for…
We haven't written up this one. bioRxiv has the full story — the link below goes straight to it.
