Publication Date
8-9-2023
Journal
Cell Genomics
DOI
10.1016/j.xgen.2023.100376
PMID
37601978
PMCID
PMC10435373
PubMedCentral® Posted Date
8-9-2023
PubMedCentral® Full Text Version
Post-print
Published Open-Access
yes
Abstract
Detection of organismal mosaic states for variant alleles faces technical and analytical challenges, as does the association of such variant alleles with susceptibility to neurologic disease. In this issue of Cell Genomics, Maury et al.1 reanalyze genotyping arrays of a schizophrenia cohort providing evidence for the contribution of somatic structural variant mutagenesis and rare variant alleles.
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