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Web-based design and analysis tools for CRISPR base editing.


ABSTRACT:

Background

As a result of its simplicity and high efficiency, the CRISPR-Cas system has been widely used as a genome editing tool. Recently, CRISPR base editors, which consist of deactivated Cas9 (dCas9) or Cas9 nickase (nCas9) linked with a cytidine or a guanine deaminase, have been developed. Base editing tools will be very useful for gene correction because they can produce highly specific DNA substitutions without the introduction of any donor DNA, but dedicated web-based tools to facilitate the use of such tools have not yet been developed.

Results

We present two web tools for base editors, named BE-Designer and BE-Analyzer. BE-Designer provides all possible base editor target sequences in a given input DNA sequence with useful information including potential off-target sites. BE-Analyzer, a tool for assessing base editing outcomes from next generation sequencing (NGS) data, provides information about mutations in a table and interactive graphs. Furthermore, because the tool runs client-side, large amounts of targeted deep sequencing data (ConclusionWe develop two useful web tools to design target sequence (BE-Designer) and to analyze NGS data from experimental results (BE-Analyzer) for CRISPR base editors.

SUBMITTER: Hwang GH 

PROVIDER: S-EPMC6307267 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Publications

Web-based design and analysis tools for CRISPR base editing.

Hwang Gue-Ho GH   Park Jeongbin J   Lim Kayeong K   Kim Sunghyun S   Yu Jihyeon J   Yu Eunchong E   Kim Sang-Tae ST   Eils Roland R   Kim Jin-Soo JS   Bae Sangsu S  

BMC bioinformatics 20181227 1


<h4>Background</h4>As a result of its simplicity and high efficiency, the CRISPR-Cas system has been widely used as a genome editing tool. Recently, CRISPR base editors, which consist of deactivated Cas9 (dCas9) or Cas9 nickase (nCas9) linked with a cytidine or a guanine deaminase, have been developed. Base editing tools will be very useful for gene correction because they can produce highly specific DNA substitutions without the introduction of any donor DNA, but dedicated web-based tools to fa  ...[more]

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