Sort by
Refine Your Search
-
variation in breast cancer susceptibility using whole genome sequencing data”. This project will investigate the contribution of rare non‑coding regulatory variants, including those in enhancers, promoters
-
work on the project “Assessing the role of rare germline non-coding genetic variation in breast cancer susceptibility using whole genome sequencing data”. This project will investigate the contribution
Searches related to multiple sequence alignment
Enter an email to receive alerts for multiple-sequence-alignment positions