
Unraveling genomic mysteries: Sniffles2 and the quest for accurate structural variant calling
In the intricate landscape of genomics, uncovering structural variations (SVs) within the genome is akin…
In the intricate landscape of genomics, uncovering structural variations (SVs) within the genome is akin…
Advances in affordable transcriptome sequencing combined with better exon and gene prediction has motivated many…
Up to 75% of the human genome encodes RNAs. The function of many non-coding RNAs…
Single-cell RNA-sequencing (scRNA-seq) has been widely used for disease studies, where sample batches are collected…
Next generation RNA sequencing allows alternative splicing (AS) quantification with unprecedented resolution, with the relative…
N6-methyladenosine (m6A) is the most abundant internal eukaryotic mRNA modification, and is involved in the…
Cluster analysis is one of the most widely used exploratory methods for visualization and grouping…
Genetic regulation of gene expression is a complex process, with genetic effects known to vary…
The advent of single-cell RNA sequencing (scRNA-seq) has revolutionized our understanding of cellular heterogeneity and…
With the growing number of single-cell datasets collected under more complex experimental conditions, there is…