Reproducible image-based profiling with Pycytominer.

Erik Serrano,Srinivas Niranj Chandrasekaran, Dave Bunten, Kenneth I Brewer, Jenna Tomkinson, Roshan Kern,Michael Bornholdt, Stephen Fleming, Ruifan Pei, John Arevalo, Hillary Tsang,Vincent Rubinetti,Callum Tromans-Coia,Tim Becker,Erin Weisbart,Charlotte Bunne,Alexandr A Kalinin,Rebecca Senft, Stephen J Taylor,Nasim Jamali,Adeniyi Adeboye, Hamdah Shafqat Abbasi,Allen Goodman,Juan C Caicedo,Anne E Carpenter,Beth A Cimini,Shantanu Singh,Gregory P Way

ArXiv(2023)

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摘要
Technological advances in high-throughput microscopy have facilitated the acquisition of cell images at a rapid pace, and data pipelines can now extract and process thousands of image-based features from microscopy images. These features represent valuable single-cell phenotypes that contain information about cell state and biological processes. The use of these features for biological discovery is known as image-based or morphological profiling. However, these raw features need processing before use and image-based profiling lacks scalable and reproducible open-source software. Inconsistent processing across studies makes it difficult to compare datasets and processing steps, further delaying the development of optimal pipelines, methods, and analyses. To address these issues, we present Pycytominer, an open-source software package with a vibrant community that establishes an image-based profiling standard. Pycytominer has a simple, user-friendly Application Programming Interface (API) that implements image-based profiling functions for processing high-dimensional morphological features extracted from microscopy images of cells. Establishing Pycytominer as a standard image-based profiling toolkit ensures consistent data processing pipelines with data provenance, therefore minimizing potential inconsistencies and enabling researchers to confidently derive accurate conclusions and discover novel insights from their data, thus driving progress in our field.
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