Arriba is a tool for detecting gene fusions from RNA-Seq data. It uses reads that map discordantly to the reference genome to identify potential fusion events. Arriba then filters these events based on various criteria, such as supporting reads and database annotations, to provide a prioritized list of high-confidence gene fusions. It is commonly used in cancer research to identify novel therapeutic targets and understand cancer pathogenesis.
Whether you're looking to get your foot in the door, find the right person to talk to, or close the deal — accurate, detailed, trustworthy, and timely information about the organization you're selling to is invaluable.
Use Sumble to: