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CSF PBAT methylome profiling in multiple sclerosis - shallow seq

This study contains shallow-depth post-bisulfite adaptor tagging (PBAT) whole-genome bisulfite sequencing data generated from cerebrospinal fluid (CSF) cells from individuals with relapsing-remitting multiple sclerosis and neurological disease controls. The shallow-sequencing dataset includes lower-depth technical replicate sequencing of discovery-cohort samples and an independent validation cohort. These data were generated to assess the reproducibility of candidate MS-associated DNA methylation differences identified by deep PBAT-seq and to support validation of methylation signatures in CSF immune cells. The study contributes to the characterization of immune regulatory, adhesion, migration and protocadherin-associated epigenetic changes in multiple sclerosis.

Publications Citations
DNA methylation landscape of cerebrospinal fluid cells in multiple sclerosis: an epigenome-wide association study.
EBioMedicine 131: 2026 106454
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