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CRIS.py: A Versatile and High-throughput Analysis Program for CRISPR-based Genome Editing
CRISPR-Cas9 technology allows the creation of user-defined genomic modifications in cells and whole organisms. However, quantifying editing rates in pools of cells or identifying correctly edited clones is tedious. Targeted next-generation sequencing provides a high-throughput platform for optimizin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414496/ https://www.ncbi.nlm.nih.gov/pubmed/30862905 http://dx.doi.org/10.1038/s41598-019-40896-w |
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author | Connelly, Jon P. Pruett-Miller, Shondra M. |
author_facet | Connelly, Jon P. Pruett-Miller, Shondra M. |
author_sort | Connelly, Jon P. |
collection | PubMed |
description | CRISPR-Cas9 technology allows the creation of user-defined genomic modifications in cells and whole organisms. However, quantifying editing rates in pools of cells or identifying correctly edited clones is tedious. Targeted next-generation sequencing provides a high-throughput platform for optimizing editing reagents and identifying correctly modified clones, but the large amount of data produced can be difficult to analyze. Here, we present CRIS.py, a simple and highly versatile python-based program which concurrently analyzes next-generation sequencing data for both knock-out and multiple user-specified knock-in modifications from one or many edited samples. Compared to available NGS analysis programs for CRISPR based-editing, CRIS.py has many advantages: (1) the ability to analyze from one to thousands of samples at once, (2) the capacity to check each sample for multiple sequence modifications, including those induced by base-editors, (3) an output in an easily searchable file format enabling users to quickly sort through and identify correctly targeted clones. |
format | Online Article Text |
id | pubmed-6414496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64144962019-03-14 CRIS.py: A Versatile and High-throughput Analysis Program for CRISPR-based Genome Editing Connelly, Jon P. Pruett-Miller, Shondra M. Sci Rep Article CRISPR-Cas9 technology allows the creation of user-defined genomic modifications in cells and whole organisms. However, quantifying editing rates in pools of cells or identifying correctly edited clones is tedious. Targeted next-generation sequencing provides a high-throughput platform for optimizing editing reagents and identifying correctly modified clones, but the large amount of data produced can be difficult to analyze. Here, we present CRIS.py, a simple and highly versatile python-based program which concurrently analyzes next-generation sequencing data for both knock-out and multiple user-specified knock-in modifications from one or many edited samples. Compared to available NGS analysis programs for CRISPR based-editing, CRIS.py has many advantages: (1) the ability to analyze from one to thousands of samples at once, (2) the capacity to check each sample for multiple sequence modifications, including those induced by base-editors, (3) an output in an easily searchable file format enabling users to quickly sort through and identify correctly targeted clones. Nature Publishing Group UK 2019-03-12 /pmc/articles/PMC6414496/ /pubmed/30862905 http://dx.doi.org/10.1038/s41598-019-40896-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Connelly, Jon P. Pruett-Miller, Shondra M. CRIS.py: A Versatile and High-throughput Analysis Program for CRISPR-based Genome Editing |
title | CRIS.py: A Versatile and High-throughput Analysis Program for CRISPR-based Genome Editing |
title_full | CRIS.py: A Versatile and High-throughput Analysis Program for CRISPR-based Genome Editing |
title_fullStr | CRIS.py: A Versatile and High-throughput Analysis Program for CRISPR-based Genome Editing |
title_full_unstemmed | CRIS.py: A Versatile and High-throughput Analysis Program for CRISPR-based Genome Editing |
title_short | CRIS.py: A Versatile and High-throughput Analysis Program for CRISPR-based Genome Editing |
title_sort | cris.py: a versatile and high-throughput analysis program for crispr-based genome editing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414496/ https://www.ncbi.nlm.nih.gov/pubmed/30862905 http://dx.doi.org/10.1038/s41598-019-40896-w |
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