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CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting
Analysis of CRISPR-induced mutations at targeted locus can be achieved by polymerase chain reaction amplification followed by parallel massive sequencing. We developed a novel algorithm, named as CRISPRpic, to analyze the sequencing reads for the CRISPR experiments via counting exact-matching and pa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034628/ https://www.ncbi.nlm.nih.gov/pubmed/32118203 http://dx.doi.org/10.1093/nargab/lqaa012 |
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author | Lee, HoJoon Chang, Howard Y Cho, Seung Woo Ji, Hanlee P |
author_facet | Lee, HoJoon Chang, Howard Y Cho, Seung Woo Ji, Hanlee P |
author_sort | Lee, HoJoon |
collection | PubMed |
description | Analysis of CRISPR-induced mutations at targeted locus can be achieved by polymerase chain reaction amplification followed by parallel massive sequencing. We developed a novel algorithm, named as CRISPRpic, to analyze the sequencing reads for the CRISPR experiments via counting exact-matching and pattern-searching. Compare to the other methods based on sequence alignment, CRISPRpic provides precise mutation calling and ultrafast analysis of the sequencing results. Python script of CRISPRpic is available at https://github.com/compbio/CRISPRpic. |
format | Online Article Text |
id | pubmed-7034628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70346282020-02-26 CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting Lee, HoJoon Chang, Howard Y Cho, Seung Woo Ji, Hanlee P NAR Genom Bioinform Methart Analysis of CRISPR-induced mutations at targeted locus can be achieved by polymerase chain reaction amplification followed by parallel massive sequencing. We developed a novel algorithm, named as CRISPRpic, to analyze the sequencing reads for the CRISPR experiments via counting exact-matching and pattern-searching. Compare to the other methods based on sequence alignment, CRISPRpic provides precise mutation calling and ultrafast analysis of the sequencing results. Python script of CRISPRpic is available at https://github.com/compbio/CRISPRpic. Oxford University Press 2020-02-21 /pmc/articles/PMC7034628/ /pubmed/32118203 http://dx.doi.org/10.1093/nargab/lqaa012 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial 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 | Methart Lee, HoJoon Chang, Howard Y Cho, Seung Woo Ji, Hanlee P CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting |
title | CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting |
title_full | CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting |
title_fullStr | CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting |
title_full_unstemmed | CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting |
title_short | CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting |
title_sort | crisprpic: fast and precise analysis for crispr-induced mutations via prefixed index counting |
topic | Methart |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034628/ https://www.ncbi.nlm.nih.gov/pubmed/32118203 http://dx.doi.org/10.1093/nargab/lqaa012 |
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