Jeong, H.H. et. al. (2017) Bioinformatics, btx335. https://www.ncbi.nlm.nih.gov/pubmed/28541456
Analyzing next generation sequencing data from pooled screening experiments can be a difficult and time-consuming process, with few programs providing a user-friendly interface and presentation of data. Researchers from the Texas Children’s Hospital have developed a cloud based system for analysis, deconvolution, and presentation of sequencing data – allowing researchers to quickly determine the frequency and types of mutations.