bioRxiv Science⌕ Search

Biology subjects

Sancho Zamora, J.

Publications and source records attributed to Sancho Zamora, J..

2 recordsLinked to original sources

JIND-Multi: Leveraging Multiple Labeled Datasets for Automated Annotation of Single-Cell RNA and ATAC Data

BackgroundThe creation of single-cell atlases is essential for understanding cellular diversity and heterogeneity. However, assembling these atlases is challenging due to batch effects and the need for accurate cell annotation. Current methods for single-cell RNA and ATAC sequencing, while effective for integration, are not optimized for cell annotation. Additionally, many annotation tools rely on external databases or reference scRNA-Seq datasets, which may limit their adaptability to specific study needs, especially for rare cell-types or scATAC-Seq data. ResultsWe introduce JIND-Multi, an extended version of the JIND framework, designed to transfer cell-type labels across multiple annotated datasets. JIND-Multi significantly reduces the proportion of unclassified cells in single-cell RNA sequencing (scRNA-Seq) data while maintaining the accuracy and performance of the original JIND model. Furthermore, JIND-Multi demonstrates robust and precise annotation results in its inaugural application to scATAC-Seq data, proving its versatility and effectiveness across different single-cell sequencing technologies. ConclusionsJIND-Multi represents an improvement in cell annotation, reducing unassigned cells and offering a reliable solution for both scRNA-Seq and scATAC-Seq data. Its ability to handle multiple labeled datasets enhances the precision of annotations, making it a valuable tool for the single-cell research community. JIND-Multi is publicly available at:https://github.com/ML4BM-Lab/JIND-Multi.git.

bioinformatics↗

DeepRBP: A novel deep neural network for inferring splicing regulation

MotivationAlternative splicing plays a pivotal role in various biological processes. In the context of cancer, aberrant splicing patterns can lead to disease progression and treatment resistance. Understanding the regulatory mechanisms underlying alternative splicing is crucial for elucidating disease mechanisms and identifying potential therapeutic targets. ResultsWe present DeepRBP, a deep learning (DL) based framework to identify potential RNA-binding proteins (RBP)-Gene regulation pairs for further in-vitro validation. DeepRBP is composed of a DL model that predicts transcript abundance given RBP and gene expression data coupled with an explainability module that computes informative RBP-Gene scores. We show that the proposed framework is able to identify known RBP-Gene regulations, demonstrating its applicability to identify new ones. Availability and ImplementationDeepRBP is implemented in PyTorch, and all the code and material used in this work is available at https://github.com/ML4BM-Lab/DeepRBP. Contactiochoal@unav.es Supplementary informationSupplementary data are available at Bioinformatics online.

bioinformatics↗