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Cited by 37CRISPR and Genetic EngineeringRNA regulation and diseasePluripotent Stem Cells Research

The DOI matches its Crossref record.

Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing

Open access
Veres, Adrian, Gosis, Bridget S., Ding, Qiurong, Collins, Ryan, Ragavendran, Ashok, Brand, Harrison, Erdin, Serkan, Cowan, Chad A., Talkowski, Michael E., Musunuru, Kiran·2014·Cell stem cell
DOI 10.1016/j.stem.2014.07.009
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Crossref · 10.1016/j.stem.2014.07.009

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  • WGS can directly uncover desired and unwanted editing events by comparing genome sequences before and after CRISPR/Cas9 editing.

    “By comparing the genome sequences before and after CRISPR/Cas9 editing, WGS can directly uncover desired and unwanted editing events.”

    From Off-target effects in CRISPR/Cas9 gene editing (2023) · cites this paper as Veres et al., 2014

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Metadata

Authors
Veres, A., Gosis, B. S., Ding, Q., Collins, R., Ragavendran, A., Brand, H., Erdin, S., Cowan, C. A., Talkowski, M. E., & Musunuru, K.
Corresponding author
Musunuru, Kiran
ORCID
Venue
Cell stem cell
Publisher
Elsevier BV
Published
2014-08
Volume
15
Issue
2
Pages
254
ISSN
  • 1875-9777 (ISSN-L)
  • 1934-5909
DOI
10.1016/j.stem.2014.07.009
OpenAlex
W4241813303
Cited by
37
References
0
Citations by year
2024: 4 · 2023: 4 · 2022: 5 · 2021: 4 · 2020: 1 · 2019: 3 · 2018: 7 · 2017: 5 · 2016: 2 · 2015: 1 · 2014: 1
FWCI
1.23
Type
journal article
Language
en
Open access
Licence
Locations
Cell stem cell (publishedVersion)
Funders
Broad Institute
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
Keywords
off-target mutagenesis, CRISPR/Cas9, TALEN, genome editing, human pluripotent stem cells, single-cell genotyping, whole genome sequencing

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