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GenomeCRISPR - a database for high-throughput CRISPR/Cas9 screens
Over the past years, CRISPR/Cas9 mediated genome editing has developed into a powerful tool for modifying genomes in various organisms. In high-throughput screens, CRISPR/Cas9 mediated gene perturbations can be used for the systematic functional analysis of whole genomes. Discoveries from such scree...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210668/ https://www.ncbi.nlm.nih.gov/pubmed/27789686 http://dx.doi.org/10.1093/nar/gkw997 |
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author | Rauscher, Benedikt Heigwer, Florian Breinig, Marco Winter, Jan Boutros, Michael |
author_facet | Rauscher, Benedikt Heigwer, Florian Breinig, Marco Winter, Jan Boutros, Michael |
author_sort | Rauscher, Benedikt |
collection | PubMed |
description | Over the past years, CRISPR/Cas9 mediated genome editing has developed into a powerful tool for modifying genomes in various organisms. In high-throughput screens, CRISPR/Cas9 mediated gene perturbations can be used for the systematic functional analysis of whole genomes. Discoveries from such screens provide a wealth of knowledge about gene to phenotype relationships in various biological model systems. However, a database resource to query results efficiently has been lacking. To this end, we developed GenomeCRISPR (http://genomecrispr.org), a database for genome-scale CRISPR/Cas9 screens. Currently, GenomeCRISPR contains data on more than 550 000 single guide RNAs (sgRNA) derived from 84 different experiments performed in 48 different human cell lines, comprising all screens in human cells using CRISPR/Cas published to date. GenomeCRISPR provides data mining options and tools, such as gene or genomic region search. Phenotypic and genome track views allow users to investigate and compare the results of different screens, or the impact of different sgRNAs on the gene of interest. An Application Programming Interface (API) allows for automated data access and batch download. As more screening data will become available, we also aim at extending the database to include functional genomic data from other organisms and enable cross-species comparisons. |
format | Online Article Text |
id | pubmed-5210668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-52106682017-01-05 GenomeCRISPR - a database for high-throughput CRISPR/Cas9 screens Rauscher, Benedikt Heigwer, Florian Breinig, Marco Winter, Jan Boutros, Michael Nucleic Acids Res Database Issue Over the past years, CRISPR/Cas9 mediated genome editing has developed into a powerful tool for modifying genomes in various organisms. In high-throughput screens, CRISPR/Cas9 mediated gene perturbations can be used for the systematic functional analysis of whole genomes. Discoveries from such screens provide a wealth of knowledge about gene to phenotype relationships in various biological model systems. However, a database resource to query results efficiently has been lacking. To this end, we developed GenomeCRISPR (http://genomecrispr.org), a database for genome-scale CRISPR/Cas9 screens. Currently, GenomeCRISPR contains data on more than 550 000 single guide RNAs (sgRNA) derived from 84 different experiments performed in 48 different human cell lines, comprising all screens in human cells using CRISPR/Cas published to date. GenomeCRISPR provides data mining options and tools, such as gene or genomic region search. Phenotypic and genome track views allow users to investigate and compare the results of different screens, or the impact of different sgRNAs on the gene of interest. An Application Programming Interface (API) allows for automated data access and batch download. As more screening data will become available, we also aim at extending the database to include functional genomic data from other organisms and enable cross-species comparisons. Oxford University Press 2017-01-04 2016-10-26 /pmc/articles/PMC5210668/ /pubmed/27789686 http://dx.doi.org/10.1093/nar/gkw997 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Database Issue Rauscher, Benedikt Heigwer, Florian Breinig, Marco Winter, Jan Boutros, Michael GenomeCRISPR - a database for high-throughput CRISPR/Cas9 screens |
title | GenomeCRISPR - a database for high-throughput CRISPR/Cas9 screens |
title_full | GenomeCRISPR - a database for high-throughput CRISPR/Cas9 screens |
title_fullStr | GenomeCRISPR - a database for high-throughput CRISPR/Cas9 screens |
title_full_unstemmed | GenomeCRISPR - a database for high-throughput CRISPR/Cas9 screens |
title_short | GenomeCRISPR - a database for high-throughput CRISPR/Cas9 screens |
title_sort | genomecrispr - a database for high-throughput crispr/cas9 screens |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210668/ https://www.ncbi.nlm.nih.gov/pubmed/27789686 http://dx.doi.org/10.1093/nar/gkw997 |
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