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PinAPL-Py: A comprehensive web-application for the analysis of CRISPR/Cas9 screens.
Spahn, Philipp N; Bath, Tyler; Weiss, Ryan J; Kim, Jihoon; Esko, Jeffrey D; Lewis, Nathan E; Harismendy, Olivier.
Afiliación
  • Spahn PN; School of Medicine, Department of Pediatrics, University of California San Diego, La Jolla, CA, USA.
  • Bath T; Novo Nordisk Foundation Center for Biosustainability at UCSD, University of California San Diego, La Jolla, CA, USA.
  • Weiss RJ; Division of Biomedical Informatics, University of California San Diego, La Jolla, CA, USA.
  • Kim J; Glycobiology Research and Training Center, Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
  • Esko JD; Division of Biomedical Informatics, University of California San Diego, La Jolla, CA, USA.
  • Lewis NE; Glycobiology Research and Training Center, Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
  • Harismendy O; School of Medicine, Department of Pediatrics, University of California San Diego, La Jolla, CA, USA. n4lewis@ucsd.edu.
Sci Rep ; 7(1): 15854, 2017 Nov 20.
Article en En | MEDLINE | ID: mdl-29158538
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. 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. 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 and test datasets.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Programas Informáticos / Pruebas Genéticas / Biología Computacional / Sistemas CRISPR-Cas Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Programas Informáticos / Pruebas Genéticas / Biología Computacional / Sistemas CRISPR-Cas Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos