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Most information on somatic mutations has come from studying clonally amplified mutant cells, based on a growth advantage or genetic drift. However, almost all somatic mutations are unique for each cell and the quantitative analysis of such low- abundance mutations in normal tissues remains a major challenge in biology. Here we introduce Single Molecule Mutation Sequencing (SMM-Seq), a novel approach for quantitative identification of point mutations in normal cells and tissues.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name></name><description>Single molecule, quantitative detection of low-abundance somatic mutations by high- throughput sequencing</description><dates><last_updated>2023-05-17</last_updated><first_public>2022-10-07</first_public></dates><accession>PRJNA758911</accession><cross_references/></HashMap>