Additional file 4 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome
Description
Additional file 4: Table S3. PHMDS DMRs: Details for each DMR listed include: chromosome, start and end, width, number of CpGs, statistical significance (Stouffer and Fisher test), distance to nearest CpG island, distance to nearest gene and where available overlapping gene/s.
Publication Date
1-1-2021
Publisher
figshare Academic Research System
DOI
10.6084/m9.figshare.13533181.v1
Document Type
Data Set
Recommended Citation
Phelan, K.; Schenkel, L.C.; Boccuto, L.; DuPont, B.; Cappuccio, G.; Jain, L.; Kerkhof, J.; Aref-Eshghi, E.; Pauly, R.; Rogers, R.C.; Sarasua, S.M.; Brunetti-Pierri, N.; Levy, M.A.; McConkey, H.; Rooney, K.; Schwartz, C.E.; Sadikovic, B. (2021), "Additional file 4 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome", figshare Academic Research System, doi: 10.6084/m9.figshare.13533181.v1
https://doi.org/10.6084/m9.figshare.13533181.v1
Identifier
10.6084/m9.figshare.13533181.v1
Embargo Date
1-1-2021