Somatic mutation landscapes at single-molecule resolution | Nature
NanoSeq is used to detect mutations in single DNA molecules and analyses show that mutational processes that are independent of cell division are important contributors to somatic mutagenesis.
Data availability Information on data availability for all samples is available in Supplementary Table 1. NanoSeq sequencing data have been deposited in the European Genome-phenome Archive (EGA; https://www.ebi.ac.uk/ega/) under accession number EGAD00001006459. Sperm samples are available from the EGA under accession number EGAD00001007028. Standard sequencing data have been deposited in the EGA under accession number EGAD00001006595. For publicly available samples, references to the original sources are provided in Supplementary Table 1. Substitution and indel rates are available in…
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