GraphVelo allows for accurate inference of multimodal velocities and molecular mechanisms for single cells
编号:49 访问权限:仅限参会人 更新:2025-03-25 14:08:06 浏览:34次 口头报告

报告开始:2025年03月29日 16:20(Asia/Shanghai)

报告时间:20min

所在会场:[S5] 一作面对面论坛(交叉) [S5] 一作面对面论坛(交叉)

暂无文件

摘要
RNA velocities and any of further developed methods have their own inherent limitations that have impeded further development of the single cell field and have never been properly addressed: 
1. RNA velocities cannot be reliably inferred for a large portion of genes, which can be a serious limitation esp. for transcription factors typically in low expression.
2. Splicing-based RNA velocities cannot be applied to virus genome.
3. The framework is restricted to transcriptomic data, and it is unclear how to generalize the framework to the accumulating multi-omic data. MultiVelo (Nat Biotech 2023) is one method proposed. However, as you can see from some examples we analyzed in this manuscript (Extended Data Figure 12a & c), the chromatin dynamics MultiVelo predicted by the inferred velocities is often opposite to the actual trend of change revealed by the scATACseq modality of the same dataset. That is, the method is even not self-consistent. 
4. There is no quantitative and rigorous method to transform velocities between different representations. This issue has been heated discussed in the single cell community, and is identified as a major criticism on current practice in the field. 
In this work we provided a general framework to address those limitations. Our approach is based on dynamical systems theories, differential geometry, and topology theories of manifolds. It is based on a fundamental property that single cell data fall to a low-dimensional manifold, which also impose a geometric constraint on the velocity vectors based on dynamical systems theory. The existence of low-dimensional manifold is essentially the foundation of machine learning for learning unknowns from partial information. Here it allows GraphVelo to resolve the above-mentioned limitations.  
We have tested on multiple synthetic and real scRNAseq/multi-omic datasets. By combining with and extending the original Dynamo analyses, we provided detailed mechanistic information on various cellular processes supported by the existing literature, well beyond what other dominating approaches typically provide. We performed systematic benchmark studies to evaluate the performance of the present method and several existing dominant approaches in the field
关键词
暂无
报告人
陈俞皓
浙江大学

发表评论
验证码 看不清楚,更换一张
全部评论
重要日期
  • 会议日期

    03月28日

    2025

    03月30日

    2025

  • 04月15日 2025

    注册截止日期

主办单位
中国生物信息学学会基因组信息学专业委员会
承办单位
中国农业科学院农业基因组研究所
大鹏湾实验室
联系方式
移动端
在手机上打开
小程序
打开微信小程序
客服
扫码或点此咨询