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PinAPL-Py: A comprehensive web-application for the analysis of CRISPR/Cas9 screens

Philipp N. Spahn, Tyler Bath, Ryan J. Weiss, Jihoon Kim, Jeffrey D. Esko, Nathan E. Lewis, Olivier Harismendy
doi: https://doi.org/10.1101/147462
Philipp N. Spahn
1School of Medicine, Department of Pediatrics, La Jolla, CA
2Novo Nordisk Foundation Center for Biosustainability at UCSD, La Jolla, CA
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Tyler Bath
4Division of Biomedical Informatics, La Jolla, CA
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Ryan J. Weiss
3Glycobiology Research and Training Center, Department of Cellular and Molecular Medicine, La Jolla, CA
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Jihoon Kim
4Division of Biomedical Informatics, La Jolla, CA
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Jeffrey D. Esko
3Glycobiology Research and Training Center, Department of Cellular and Molecular Medicine, La Jolla, CA
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Nathan E. Lewis
1School of Medicine, Department of Pediatrics, La Jolla, CA
2Novo Nordisk Foundation Center for Biosustainability at UCSD, La Jolla, CA
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Olivier Harismendy
4Division of Biomedical Informatics, La Jolla, CA
5Moores Cancer Center, Department of Medicine, University of California San Diego, La Jolla, CA
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Abstract

Background Large-scale genetic screens using CRISPR/Cas9 technology have emerged as a major tool for functional genomics. With its increased popularity, experimental biologists frequently acquire large sequencing datasets for which they often do not have an easy analysis option. While a few bioinformatic tools have been developed for this purpose, their utility is still hindered either due to limited functionality or the requirement of bioinformatic expertise.

Results To make sequencing data analysis of CRISPR/Cas9 screens more accessible to a wide range of scientists, we developed a Platform-independent Analysis of Pooled Screens using Python (PinAPL-Py), which is operated as an intuitive web-service. PinAPL-Py implements state-of-the-art tools and statistical models, assembled in a comprehensive workflow covering sequence quality control, automated sgRNA sequence extraction, alignment, sgRNA enrichment/depletion analysis and gene ranking. The workflow is set up to use a variety of popular sgRNA libraries as well as custom libraries that can be easily uploaded. Various analysis options are offered, suitable to analyze a large variety of CRISPR/Cas9 screening experiments. Analysis output includes ranked lists of sgRNAs and genes, and publication-ready plots.

Conclusions PinAPL-Py helps to advance genome-wide screening efforts by combining comprehensive functionality with user-friendly implementation. PinAPL-Py is freely accessible at http://pinapl-py.ucsd.edu with instructions, documentation and test datasets. The source code is available at https://github.com/LewisLabUCSD/PinAPL-Py

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted July 27, 2017.
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PinAPL-Py: A comprehensive web-application for the analysis of CRISPR/Cas9 screens
Philipp N. Spahn, Tyler Bath, Ryan J. Weiss, Jihoon Kim, Jeffrey D. Esko, Nathan E. Lewis, Olivier Harismendy
bioRxiv 147462; doi: https://doi.org/10.1101/147462
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PinAPL-Py: A comprehensive web-application for the analysis of CRISPR/Cas9 screens
Philipp N. Spahn, Tyler Bath, Ryan J. Weiss, Jihoon Kim, Jeffrey D. Esko, Nathan E. Lewis, Olivier Harismendy
bioRxiv 147462; doi: https://doi.org/10.1101/147462

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