Posts Tagged: NGS

miRNAs+Barcodes_V01

Webinar highlights – Maximizing miRNA-seq success from liquid biopsy samples

Development of markers that facilitate earlier and non-invasive diagnosis is a primary goal of disease research. This is where microRNAs come in. Studies have indicated that the expression levels of these non-coding RNA molecules are altered in disease states, including cancer and neurodegeneration. Evidence of their presence in biofluids means that their potential as important… Read article →




Biogenesis

Eliminating contaminants in miRNA-seq libaries just got easier

microRNA sequencing is not only useful for finding novel microRNAs and detecting isomiRs; it’s also an attractive method for miRNA expression profiling, particularly when combined with molecular indexing to boost quantification accuracy (see our previous post, Barcodes in NGS: sample vs molecular). But preparing a library to sequence purely microRNAs can be difficult due to contaminating… Read article →


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Join our webinar: State-of-the-art NGS library quality control solutions

Next-generation sequencing (NGS) is revolutionizing life science research and healthcare. The advent of multiple platforms has opened the doors to increased throughput, speed, sensitivity and flexibility, providing researchers with valuable insights at an unprecedented rate. While recent technological developments have made NGS more accessible to smaller labs, many barriers to implementation still remain. NGS workflows… Read article →