MOESM4 of Concurrent genome and epigenome editing by CRISPR-mediated sequence replacement
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Additional file 4: Table S1. Counts of reads including both inverted and forward-oriented sequences that exactly matched the promoter, exon 1, splice donor, PAM mutations, and one of the three sets of allele-defining SNVs (wild-type, methylated or unmethylated) as well as unmatched sequences.
创建时间：
2019-11-19
