Corces 2020 ATACseq

URL: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE147672

Publications: Corces, M.R., Shcherbina, A., Kundu, S. et al. Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer’s and Parkinson’s diseases. Nat Genet 52, 1158–1168 (2020). https://doi.org/10.1038/s41588-020-00721-x
 
Funding/Acknowledgements: This work was supported by National Institutes of Health (NIH) grant nos. NS062684, AG057707, AG053959, AG047366 (to T.J.M.), HG007735 (to H.Y.C.), HG009431 (to S.B.M./A.K.), AG066490 (to S.B.M.) and AG059918 (to M.R.C.). Additional support for patient sample collection was provided by NIH grant nos. AG005136 and AG019610. Sequencing data for this project were generated on an Illumina HiSeq 4000 System supported in part by NIH grant no. S10OD018220. Additional resources at the Stanford Center for Genomics and Personalized Medicine Sequencing Center were supported by NIH grant no. S10OD025212. M.R.C. is supported by the American Society of Hematology Scholar Award. A.S. is supported by the Stanford BioX Bowes fellowship. M.J.G. and T.E. are supported by a National Library of Medicine training grant no. 5T15LM007033-36. M.J.G. is additionally supported by a Stanford Graduate Fellowship. H.Y.C. is an Investigator of the Howard Hughes Medical Institute.