Back

Detecting local changes in chromatin architecture with false discovery control

Koch, H.; Yang, T.; Imakaev, M.; Hardison, R. C.; Li, Q.

2020-09-04 genomics
10.1101/2020.09.03.281972 bioRxiv
Show abstract

Hi-C experiments are a powerful means to describe the organization of chromatin interactions genome-wide. By using Hi-C data to identify differentially organized genomic regions, relationships between this organization, gene expression, and cell identity may be established. However, Hi-C data exhibit a unique and challenging spatial structure, as genomic loci can show strong correlations when they are nearby in 3D space within the nucleus or 1D space along the chromosome. Consequently, the development of methods that can accurately detect differences between Hi-C samples while controlling false discoveries has remained difficult. To meet this need, we introduce a spatial modeling approach based on sliding window statistics. Using polymer simulations, we illustrate the improved power and precision of our method to identify differentially interacting genomic regions. We further demonstrate our methods ability to reveal biologically meaningful changes in chromatin architecture through two data analyses concerning the loss of architectural and chromatin remodeling proteins.

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

50% of probability mass above

"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.