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. 2024 Sep 14;2:101894. doi: 10.1016/j.gimo.2024.101894

Figure 1.

Figure 1

Regulatorygenome sequencinganalyses. Rare single-nucleotide variants that overlap brain-specific transcription factor binding sites were interrogated and subjected to deep learning analyses. Predicted gene targets were analyzed on the level of pathways as well as brain-specific functional networks. Rare copy-number variants were analyzed for their proximity to human embryonic stem cell topologically associating domain boundaries.