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Paper Details

CADD-Splice-improving genome-wide variant effect prediction using deep learning-derived splice scores.
Genome Med
312
2021
CADD, dinucleotides, donor and acceptor dinucleotides, genetic disease, genome, genomic, genomic exons, human, mRNAs, splice variants
Author NameAffiliation
Max SchubachCharite - Universitatsmedizin Berlin
Max SchubachBerlin Institute of Health (BIH)
Jay ShendureUniversity of Washington
Jay ShendureUniversity of Washington
Jay ShendureBrotman Baty Institute for Precision Medicine, University of Washington
Jay ShendureBrotman Baty Institute for Precision Medicine, University of Washington
Martin KircherCharite - Universitatsmedizin Berlin
Martin KircherBerlin Institute of Health (BIH)
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