Shipping biological materials such as RNA, cells, and tissue samples over long distances presents a number of challenges, particularly when maintaining their integrity, functionality, and biological activity is crucial. Whether for research, diagnostics, or clinical purposes, improper handling and transport conditions can lead to sample degradation, contamination, or loss of viability.
Non-coding RNAs (ncRNAs) have emerged as crucial players in gene regulation and cellular processes. Their diverse roles, including gene silencing, transcriptional regulation, and protein translation, have spurred significant interest in their study. Non-coding RNA sequencing (ncRNA-Seq) has become a powerful tool for unraveling the complexities of these molecules. This report provides an overview of the major kits and tools employed in ncRNA-Seq.
In the rapidly advancing field of genomics, RNA sequencing (RNA-seq) has become an essential tool for understanding gene expression. Two primary approaches have emerged: single-cell RNA sequencing (scRNA-seq) and bulk RNA sequencing (bulk RNA-seq). Both methods offer unique insights into transcriptomics but differ significantly in their resolution, applications, and interpretation of data. This article explores the differences between scRNA-seq and bulk RNA-seq and highlights their respective applications in research and clinical settings.
In the age of genomics, RNA sequencing (RNAseq) stands out as a transformative technology, providing deep insights into the transcriptome—the complete set of RNA transcripts produced by the genome under specific circumstances or in a particular cell. This blog will guide you through the basics of RNAseq, its applications, and the impact it has on modern biology and medicine.
