Skip to content
Open
Changes from all commits
Commits
File filter

Filter by extension

Filter by extension

Conversations
Failed to load comments.
Loading
Jump to
Jump to file
Failed to load files.
Loading
Diff view
Diff view
1 change: 1 addition & 0 deletions content/01.abstract.md
Original file line number Diff line number Diff line change
@@ -1,3 +1,4 @@
## Abstract {.page_break_before}

ZSL added for test.
Decoding the regulatory behavior of DNA sequences and the functional effects of noncoding variants is a preeminent challenge in understanding the mechanisms of gene regulation. This is also important for the genetics of common diseases, as most disease-associated variants are located in noncoding regions of the genome. Recently, Convolutional Neural Networks (CNNs) based methods have been developed to predict genome-wide chromatin profiles in various cellular contexts. However, these tools and resources were often trained in cell lines or bulk tissues that are not necessarily disease-related. This is particularly an issue for neuropsychiatric disorders, where the most relevant cell and tissue types are missing in the training data used by current tools.