Deciphering cis-regulatory elements using REgulamentary
Riva, S. G.; Georgiades, E.; Herrmann, J. C.; Gur, R.; Sanders, E.; Sergeant, M.; Baxter, M.; Hughes, J. R.
Show abstract
With the boom in Genome-Wide Association Studies (GWAS), it has become apparent that many disease-associated genetic variants lie in the non-coding regions of the genome. In order to prioritise these variants and disentangle their functional significance, it is important to be able to accurately classify cis-regulatory elements within these non-coding regions of the genome. Historically, the classification of cis-regulatory elements relied purely on the presence of characteristic histone marks, with recent advancements in their classification using more sophisticated Hidden Markov Model (HMM)-based approaches. The limitation of the HMM-based approaches is that the output of these models is an arbitrary chromatin state, which then requires the user to manually assign these states to a particular class of cis-regulatory elements. Here we present a new tool, REgulamentary, which enables de novo genome-wide annotation of cis-regulatory elements in a cell-type specific manner. We benchmarked REgulamentary against GenoSTAN, the most popular existing published chromatin annotation and regulatory element identification tool, to demonstrate the advancements REgulamentary can provide in assigning chromatin states. Finally, as an example of REgulamentarys utility in solving complex disease trait loci, we applied REgulamentary to published GWAS data to demonstrate how this tool can be used to prioritise likely causal variants.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
- Assessing the impact of transcriptomics data analysis pipelines on downstream functional enrichment results 94%
- edgeR v4: powerful differential analysis of sequencing data with expanded functionality and improved support for small counts and larger datasets 94%
- TransCRISPR - sgRNA design tool for CRISPR/Cas9 experiments targeting DNA sequence motifs 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.