Additional file 1 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome
Description
Additional file 1: Table S1. Differentially methylated probes in PHMDS samples compared to controls. For each probe, listed are: methylation % difference, p value, adjusted p value, chromosome and chromosome position, and where available overlapping UCSC Gene name, UCSC gene type and UCSC CpG island.
Publication Date
1-1-2021
Publisher
figshare Academic Research System
DOI
10.6084/m9.figshare.13533172.v1
Document Type
Data Set
Recommended Citation
Schenkel, L.C.; Levy, M.A.; Cappuccio, G.; Phelan, K.; Sarasua, S.M.; Rogers, R.C.; Boccuto, L.; Schwartz, C.E.; Aref-Eshghi, E.; Kerkhof, J.; DuPont, B.; Brunetti-Pierri, N.; Sadikovic, B.; McConkey, H.; Rooney, K.; Pauly, R.; Jain, L. (2021), "Additional file 1 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.13533172.v1
https://doi.org/10.6084/m9.figshare.13533172.v1
Identifier
10.6084/m9.figshare.13533172.v1
Embargo Date
1-1-2021