Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

dbGuide

General information

URL: https://sgrnascorer.cancer.gov/dbguide
Full name: A Database of Guide RNAs
Description: The database not only contains computationally determined candidate guide RNA sequences, but of even greater value, over 4000 sequences which have been functionally validated either through direct amplicon sequencing or manual curation of literature from over 1000 publications.
Year founded: 2021
Last update: 2020-9-1
Version: 1,0
Accessibility:
Accessible
Country/Region: United States

Classification & Tag

Data type:
RNA
Data object:
Database category:
Major species:
Keywords:

Contact information

University/Institution: Frederick National Laboratory for Cancer Research
Address:
City: Frederick
Province/State:
Country/Region: United States
Contact name (PI/Team): Raj Chari
Contact email (PI/Helpdesk): raj.chari@nih.gov

Publications

33051688
dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells. [PMID: 33051688]
Gooden AA, Evans CN, Sheets TP, Clapp ME, Chari R.

With the technology's accessibility and ease of use, CRISPR has been employed widely in many different organisms and experimental settings. As a result, thousands of publications have used CRISPR to make specific genetic perturbations, establishing in itself a resource of validated guide RNA sequences. While numerous computational tools to assist in the design and identification of candidate guide RNAs exist, these are still just at best predictions and generally, researchers inevitably will test multiple sequences for functional activity. Here, we present dbGuide (https://sgrnascorer.cancer.gov/dbguide), a database of functionally validated guide RNA sequences for CRISPR/Cas9-based knockout in human and mouse. Our database not only contains computationally determined candidate guide RNA sequences, but of even greater value, over 4000 sequences which have been functionally validated either through direct amplicon sequencing or manual curation of literature from over 1000 publications. Finally, our established framework will allow for continual addition of newly published and experimentally validated guide RNA sequences for CRISPR/Cas9-based knockout as well as incorporation of sequences from different gene editing systems, additional species and other types of site-specific functionalities such as base editing, gene activation, repression and epigenetic modification.

Nucleic Acids Res. 2021:49(D1) | 17 Citations (from Europe PMC, 2025-12-13)

Ranking

All databases:
2651/6895 (61.566%)
Literature:
242/577 (58.232%)
2651
Total Rank
17
Citations
4.25
z-index

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Record metadata

Created on: 2020-11-09
Curated by:
Lin Liu [2022-08-31]
Lin Liu [2021-02-22]
Xiaonan Liu [2020-11-26]
Xiaonan Liu [2020-11-24]
Chang Liu [2020-11-09]