4.7 Article

Cell fate conversion prediction by group sparse optimization method utilizing single-cell and bulk OMICs data

期刊

BRIEFINGS IN BIOINFORMATICS
卷 22, 期 6, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbab311

关键词

cell fate conversion; master transcription factor; group sparse optimization; integrative OMICs; gene regulatory network; single-cell genomics

资金

  1. National Natural Science Foundation of China [41606143, 12071306, 11871347]
  2. Research Grants Council, Hong Kong [17121414 M]
  3. Mayo Clinic, USA (Mayo Clinic Arizona)
  4. Natural Science Foundation of Guangdong Province of China [2019A1515011917, 2020B1515310008]
  5. Natural Science Foundation of Shenzhen [JCYJ20190808173603590]
  6. National Science Council of Taiwan [MOST 102-2115-M-039-003-MY3]
  7. China Postdoctoral Science Foundation [2019TQ0397]
  8. Mayo Clinic, USA (Center for Individualized Medicine)

向作者/读者索取更多资源

Cell fate conversion by overexpressing defined factors is a powerful tool in regenerative medicine, but identifying key factors for efficient conversion is challenging. Utilizing various OMICs data and computational methods can help predict master transcription factors for successful and complete cell fate conversion, ultimately improving the effectiveness and reducing costs of experimental processes.
Cell fate conversion by overexpressing defined factors is a powerful tool in regenerative medicine. However, identifying key factors for cell fate conversion requires laborious experimental efforts; thus, many of such conversions have not been achieved yet. Nevertheless, cell fate conversions found in many published studies were incomplete as the expression of important gene sets could not be manipulated thoroughly. Therefore, the identification of master transcription factors for complete and efficient conversion is crucial to render this technology more applicable clinically. In the past decade, systematic analyses on various single-cell and bulk OMICs data have uncovered numerous gene regulatory mechanisms, and made it possible to predict master gene regulators during cell fate conversion. By virtue of the sparse structure of master transcription factors and the group structure of their simultaneous regulatory effects on the cell fate conversion process, this study introduces a novel computational method predicting master transcription factors based on group sparse optimization technique integrating data from multi-OMICs levels, which can be applicable to both single-cell and bulk OMICs data with a high tolerance of data sparsity. When it is compared with current prediction methods by cross-referencing published and validated master transcription factors, it possesses superior performance. In short, this method facilitates fast identification of key regulators, give raise to the possibility of higher successful conversion rate and in the hope of reducing experimental cost.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据