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made by error-prone PCR, site-saturation mutagenesis and transposon-based InDel mutagenesis in vitro selections will be carried out, followed by long-read nanopore sequencing and deep mutational scanning
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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
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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
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