DeepFM-Crispr:通过深度学习预测 CRISPR 靶向效应

Condy Bao, Fuxiao Liu
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引用次数: 0

摘要

CRISPR-Cas9 是一种开创性的基因编辑技术,可通过短 RNA 引导序列对基因组进行精确修饰,自 CRISPR-Cas9 诞生以来,该技术在各个领域的普及和应用都有了显著提高。CRISPR-Cas9的成功刺激了进一步的投资,并导致了包括CRISPR-Cas13在内的其他CRISPR系统的发现。与以DNA为靶标的Cas9不同,Cas13以RNA为靶标,在基因调控方面具有独特的优势。我们重点研究了Cas13d,它是一种因其附带活性而闻名的变体,在激活时会非特异性地裂解相邻的RNA分子,这对其功能至关重要。我们介绍了 DeepFM-Crispr,这是一种新型深度学习模型,用于预测 Cas13d 的靶上效率和评估其靶外效应。该模型利用大型语言模型生成富含进化和结构数据的综合表征,从而增强了对 RNA 二级结构和 sgRNA 整体功效的预测。对比实验表明,DeepFM-Crispr 不仅超越了传统模型,而且在预测准确性和可靠性方面也优于最近最先进的深度学习方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DeepFM-Crispr: Prediction of CRISPR On-Target Effects via Deep Learning
Since the advent of CRISPR-Cas9, a groundbreaking gene-editing technology that enables precise genomic modifications via a short RNA guide sequence, there has been a marked increase in the accessibility and application of this technology across various fields. The success of CRISPR-Cas9 has spurred further investment and led to the discovery of additional CRISPR systems, including CRISPR-Cas13. Distinct from Cas9, which targets DNA, Cas13 targets RNA, offering unique advantages for gene modulation. We focus on Cas13d, a variant known for its collateral activity where it non-specifically cleaves adjacent RNA molecules upon activation, a feature critical to its function. We introduce DeepFM-Crispr, a novel deep learning model developed to predict the on-target efficiency and evaluate the off-target effects of Cas13d. This model harnesses a large language model to generate comprehensive representations rich in evolutionary and structural data, thereby enhancing predictions of RNA secondary structures and overall sgRNA efficacy. A transformer-based architecture processes these inputs to produce a predictive efficacy score. Comparative experiments show that DeepFM-Crispr not only surpasses traditional models but also outperforms recent state-of-the-art deep learning methods in terms of prediction accuracy and reliability.
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