Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 54 checked references that resolve
resolves10.1126/science.aao4426Aging and neurodegeneration are associated with increased mutations in single human neurons
resolves10.1073/pnas.1902510116Single-cell whole-genome sequencing reveals the functional landscape of somatic mutations in B lymphocytes across the human lifespan
resolves10.1038/nature19768Tissue-specific mutation accumulation in human adult stem cells during life
resolves10.1038/nmeth.4227Accurate identification of single-nucleotide variants in whole-genome-amplified single cells
resolves10.1101/211169Linked-read analysis identifies mutations in single cell DNA sequencing data
resolves10.1186/s13287-017-0628-9Extracellular vesicles from human liver stem cells restore argininosuccinate synthase deficiency
resolves10.1038/ncomms15183Differences between germline and somatic mutation rates in humans and mice
resolves10.1021/tx010032fMutagenesis by <i>O</i><sup>6</sup>-Methyl-, <i>O</i><sup>6</sup>-Ethyl-, and <i>O</i><sup>6</sup>-Benzylguanine and <i>O</i><sup>4</sup>-Methylthymine in Human Cells: Effects of <i>O</i><sup>6</sup>-Alkylguanine-DNA Alkyltransferase and Mismatch Repair
resolves10.1101/322859The Repertoire of Mutational Signatures in Human Cancer
resolves10.1038/nature11245Architecture of the human regulatory network derived from ENCODE data
resolves10.1016/j.cell.2017.09.004Single-Cell Analysis of Human Pancreas Reveals Transcriptional Signatures of Aging and Somatic Mutation Patterns
resolves10.1038/nature21065Single-cell spatial reconstruction reveals global division of labour in the mammalian liver
resolves10.1002/bit.10727Clonal expansion of adult rat hepatic stem cell lines by suppression of asymmetric cell kinetics (SACK)
resolves10.1038/nature11826In vitro expansion of single Lgr5+ liver stem cells induced by Wnt-driven regeneration
resolves10.1101/gr.107524.110The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
resolves10.1101/gr.129684.111VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
resolves10.1038/nbt.2514Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
resolves10.1002/hep.24252Hepatocyte turnover and regeneration: Virtually a virtuoso performance
resolves10.1093/nar/gkq603ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
resolves10.1093/nar/gkg509SIFT: predicting amino acid changes that affect protein function
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