45 minutes + live Q&A
Next Generation Sequencing (NGS) is a powerful technology used to profile the small RNA composition in liquid biopsies by producing large sets of sequencing reads. The challenge with this technology is the large amount of data produced, making it difficult to manually identify and measure the small RNA biotypes. To overcome this problem, bioinformatic tools with various functions such as quality filtering, adapter trimming, and read mapping are combined into a pipeline to convert the sequences into a format that is more comprehensive. Bioinformatics also incorporates other tools that can be used to compare different RNA biotypes in a sample or between samples. During this webinar, we will discuss the inputs, outputs, and parameters needed to analyze the small RNA composition in liquid biopsy samples. This helps to explore the roles that small RNAs can play as biomarkers in various diseases and health conditions. Register for FREE to learn more!