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Items: 3

1.

High-fidelity base editing mediated by Cpf1-cytidine deaminase fusion

(Submitter supplied) C-to-T base editing mediated by CRISPR/Cas9 base editors (BEs) needs a G/C-rich PAM and the editing fidelity is compromised by unwanted indels and non-C-to-T substitutions. We developed CRISPR/Cpf1-based BEs to recognize a T-rich PAM and induce efficient C-to-T editing with few indels and/or non-C-to-T substitutions. The requirement of editing fidelity in therapeutic-related trials necessitates the development of CRISPR/Cpf1-based BEs, which also facilitates base editing in A/T-rich regions.
Organism:
Homo sapiens
Type:
Other
Platform:
GPL20795
40 Samples
Download data: TXT, XLS
Series
Accession:
GSE105002
ID:
200105002
2.

HiSeq X Ten (Homo sapiens)

Platform
Accession:
GPL20795
ID:
100020795
3.

Cas9-BE2-1_2+Cas9-BE2-2_1

Organism:
Homo sapiens
Source name:
293FT cells
Platform:
GPL20795
Series:
GSE105002
Download data: TXT
Sample
Accession:
GSM2813808
ID:
302813808
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Supplemental Content

db=gds|term=GSM2813808[Accession]|query=2|qty=2|blobid=MCID_666ab2de4f49d52cd28699cc|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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