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Related Concept Videos

CRISPR01:59

CRISPR

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Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
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CRISPR and crRNAs02:53

CRISPR and crRNAs

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Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
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RNA Interference01:23

RNA Interference

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RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
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Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

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RNA Polymerase (RNAP) is conserved in all animals, with bacterial, archaeal, and eukaryotic RNAPs sharing significant sequence, structural, and functional similarities. Among the three eukaryotic RNAPs, RNA Polymerase II is most similar to bacterial RNAP in terms of both structural organization and folding topologies of the enzyme subunits. However, these similarities are not reflected in their mechanism of action.
All three eukaryotic RNAPs require specific transcription factors, of which the...
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Group Design02:01

Group Design

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The most basic experimental design involves two groups: the experimental group and the control group. The two groups are designed to be the same except for one difference— experimental manipulation. The experimental group gets the experimental manipulation—that is, the treatment or variable being tested—and the control group does not. Since experimental manipulation is the only difference between the experimental and control groups, we can be sure that any differences between...
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RNA Structure01:23

RNA Structure

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Overview
The basic structure of RNA consists of a five-carbon sugar and one of four nitrogenous bases. Although most RNA is single-stranded, it can form complex secondary and tertiary structures. Such structures play essential roles in the regulation of transcription and translation.
Different Types of RNA Have the Same Basic Structure
There are three main types of ribonucleic acid (RNA): messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). All three RNA types consist of a...
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Updated: Feb 8, 2026

DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning
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DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning

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DeepCRISPR: optimized CRISPR guide RNA design by deep learning.

Guohui Chuai1,2, Hanhui Ma3, Jifang Yan1,2

  • 1Department of Endocrinology & Metabolism, Shanghai Tenth People's Hospital, Tongji University, Shanghai, 20009, China.

Genome Biology
|June 28, 2018
PubMed
Summary
This summary is machine-generated.

DeepCRISPR accurately predicts CRISPR single guide RNA (sgRNA) knockout efficacy and off-target effects. This computational platform enhances sgRNA design for improved sensitivity and specificity in gene editing applications.

Keywords:
CRISPR systemDeep learningGene knockoutOff-targetsOn-targets

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Area of Science:

  • Genomics
  • Bioinformatics
  • Molecular Biology

Background:

  • CRISPR gene editing requires accurate prediction of single guide RNA (sgRNA) on-target efficacy and off-target profiles.
  • Current in silico tools face challenges in achieving high sensitivity and specificity for sgRNA design.

Purpose of the Study:

  • To develop a comprehensive computational platform, DeepCRISPR, for unified prediction of sgRNA on-target and off-target activities.
  • To surpass the performance of existing state-of-the-art in silico prediction tools for CRISPR sgRNAs.

Main Methods:

  • Utilized deep learning within a unified framework for sgRNA on-target and off-target site prediction.
  • Automated identification of sequence and epigenetic features influencing sgRNA knockout efficacy using a data-driven approach.

Main Results:

  • DeepCRISPR demonstrates superior performance compared to current state-of-the-art in silico tools for sgRNA efficacy and specificity prediction.
  • The platform successfully automates the identification of critical sequence and epigenetic factors impacting gene editing outcomes.

Conclusions:

  • DeepCRISPR offers a powerful computational solution for optimizing sgRNA design in CRISPR applications.
  • The platform facilitates enhanced sensitivity and specificity in gene editing by accurately predicting sgRNA performance.