| Literature DB >> 29287915 |
Albina Rahim1, Justin Meskas2, Sibyl Drissler2, Alice Yue3, Anna Lorenc4, Adam Laing4, Namita Saran4, Jacqui White5, Lucie Abeler-Dörner4, Adrian Hayday6, Ryan R Brinkman7.
Abstract
The rapid expansion of flow cytometry applications has outpaced the functionality of traditional manual analysis tools used to interpret flow cytometry data. Scientists are faced with the daunting prospect of manually identifying interesting cell populations in 50-dimensional datasets, equalling the complexity previously only reached in mass cytometry. Data can no longer be analyzed or interpreted fully by manual approaches. While automated gating has been the focus of intense efforts, there are many significant additional steps to the analytical pipeline (e.g., cleaning the raw files, event outlier detection, extracting immunophenotypes). We review the components of a customized automated analysis pipeline that can be generally applied to large scale flow cytometry data. We demonstrate these methodologies on data collected by the International Mouse Phenotyping Consortium (IMPC). CrownEntities:
Keywords: Automated analysis; Bioinformatics; Flow cytometry
Mesh:
Year: 2017 PMID: 29287915 PMCID: PMC5815930 DOI: 10.1016/j.ymeth.2017.12.015
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608