AStruct: detection of allele-specific RNA secondary structure in structuromic probing data.

BACKGROUND: Uncovering functional genetic variants from an allele-specific perspective is of paramount importance in advancing our understanding of gene regulation and genetic diseases. Recently, various allele-specific events, such as allele-specific gene expression, allele-specific methylation, and allele-specific binding, have been explored on a genome-wide scale due to the development of high-throughput sequencing methods. RNA secondary structure, which plays a crucial role in multiple RNA-associated processes like RNA modification, translation and splicing, has emerged as an essential focus of relevant research. However, tools to identify genetic variants associated with allele-specific RNA secondary structures are still lacking. RESULTS: Here, we develop a computational tool called 'AStruct' that enables us to detect allele-specific RNA secondary structure (ASRS) from RT-stop based structuromic probing data. AStruct shows robust performance in both simulated datasets and public icSHAPE datasets. We reveal that single nucleotide polymorphisms (SNPs) with higher AStruct scores are enriched in coding regions and tend to be functional. These SNPs are highly conservative, have the potential to disrupt sites involved in m6A modification or protein binding, and are frequently associated with disease. CONCLUSIONS: AStruct is a tool dedicated to invoke allele-specific RNA secondary structure events at heterozygous SNPs in RT-stop based structuromic probing data. It utilizes allelic variants, base pairing and RT-stop information under different cell conditions to detect dynamic and functional ASRS. Compared to sequence-based tools, AStruct considers dynamic cell conditions and outperforms in detecting functional variants. AStruct is implemented in JAVA and is freely accessible at: https://github.com/canceromics/AStruct .

Supervised Contrastive Learning-Based Domain Generalization Network for Cross-Subject Motor Decoding.

Developing an electroencephalogram (EEG)-based motor imagery and motor execution (MI/ME) decoding system that is both highly accurate and calibration-free for cross-subject applications remains challenging due to domain shift problem inherent in such scenario. Recent research has increasingly embraced transfer learning strategies, especially domain adaptation techniques. However, domain adaptation becomes impractical when the target subject data is either difficult to obtain or unknown. To address this issue, we propose a supervised contrastive learning-based domain generalization network (SCLDGN) for cross-subject MI/ME decoding. Firstly, the feature encoder is purposefully designed to learn the EEG discriminative feature representations. Secondly, the domain alignment based on deep correlation alignment constrains the representations distance across various domains to learn domain-invariant features. In addition, the class regularization block is proposed, where the supervised contrastive learning with domain-agnostic mixup is established to learn the class-relevant features and achieve class-level alignment. Finally, in the latent space, clusters of domain-agnostic representations from the same class are mapped closer together. Consequently, SCLDGN is capable of learning domain-invariant and class-relevant discriminative representations, which are essential for effective cross-subject decoding. Extensive experiments conducted on six MI/ME datasets demonstrate the effectiveness of the proposed method in comparison with other state-of-the-art approaches. Furthermore, ablation study and visualization analyses explain the generalization mechanism of the proposed method and also show neurophysiologically meaningful patterns related to MI/ME.

High-throughput Pore-C reveals the single-allele topology and cell type-specificity of 3D genome folding.

Canonical three-dimensional (3D) genome structures represent the ensemble average of pairwise chromatin interactions but not the single-allele topologies in populations of cells. Recently developed Pore-C can capture multiway chromatin contacts that reflect regional topologies of single chromosomes. By carrying out high-throughput Pore-C, we reveal extensive but regionally restricted clusters of single-allele topologies that aggregate into canonical 3D genome structures in two human cell types. We show that fragments in multi-contact reads generally coexist in the same TAD. In contrast, a concurrent significant proportion of multi-contact reads span multiple compartments of the same chromatin type over megabase distances. Synergistic chromatin looping between multiple sites in multi-contact reads is rare compared to pairwise interactions. Interestingly, the single-allele topology clusters are cell type-specific even inside highly conserved TADs in different types of cells. In summary, HiPore-C enables global characterization of single-allele topologies at an unprecedented depth to reveal elusive genome folding principles.