Recent research on disparate psychiatric disorders has implicated rare variants in genes involved in global gene regulation and chromatin modification, as well as many common variants located primarily in regulatory regions of the genome. Understanding precisely how these variants contribute to disease will require a deeper appreciation for the mechanisms of gene regulation in the developing and adult human brain. The PsychENCODE project aims to produce a public resource of multidimensional genomic data using tissue- and cell type–specific samples from approximately 1,000 phenotypically well-characterized, high-quality healthy and disease-affected human post-mortem brains, as well as functionally characterize disease-associated regulatory elements and variants in model systems. We are beginning with a focus on autism spectrum disorder, bipolar disorder and schizophrenia, and expect that this knowledge will apply to a wide variety of psychiatric disorders. This paper outlines the motivation and design of PsychENCODE.
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Acknowledgements
The authors would like to acknowledge and thank the tissue donors and their families. We also thank all consortium members for discussions and feedback on this document. The PsychENCODE consortium projects are funded by the US National Institute of Mental Health.
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Akbarian, S., Liu, C., Knowles, J. et al. The PsychENCODE project. Nat Neurosci 18, 1707–1712 (2015). https://doi.org/10.1038/nn.4156
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DOI: https://doi.org/10.1038/nn.4156
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