
Researchers develop RNA-Seq analysis tool for the safer design of gene editing
Scheme of safety evaluation by DANGER analysis. When off-target regions are affected by genome editing,…
Scheme of safety evaluation by DANGER analysis. When off-target regions are affected by genome editing,…
The growing number of available single-cell gene expression datasets from different species creates opportunities to…
The increasing amount of data recorded in medical research can only lead to scientific breakthroughs…
Identifying cancerous samples or cells using transcriptomic data is critical for cancer related basic research,…
Cell-cell interactions (CCIs) play critical roles in many biological processes such as cellular differentiation, tissue…
Machine learning methods, particularly neural networks trained on large datasets, are transforming how scientists approach…
Alternative polyadenylation is a main driver of transcriptome diversity in mammals, generating transcript isoforms with…
Single-cell RNA-seq (scRNA-seq) analysis of multiple samples separately can be costly and lead to batch…
Existing genomic sequencing data can be used to study host–microbiome ecosystems; however, distinguishing signals that…
Carcinoma of unknown primary (CUP) is a type of metastatic cancer with tissue-of-origin (TOO) unidentifiable…