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AI 根据所提供的论文材料归类:摘要研究生物信息学贝叶斯聚类;共同调控基因的应用不足以归入经济网络与干扰细分。

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关注这篇论文的作者
Shane T Jensen
Jun S Liu

转录因子结合基序的贝叶斯聚类

研究问题
如何依据核苷酸组成相似性对转录因子结合基序聚类,同时考虑基序内部和基序之间的变异、聚类数及核心宽度的不确定性?
方法与思路
作者构造贝叶斯层级模型,使用允许聚类数变化的 Dirichlet 过程先验及可变核心宽度扩展,通过 Gibbs 抽样分析基序矩阵。
材料陈述的贡献
摘要称,模型识别出更细的基序群组,可整理转录因子并减少数据库冗余;随机实现也用于检查结果变异及替代先验的影响。
阅读关注点
应核对基序相似性的概率定义、核心宽度如何估计和抽样收敛,并查看聚类不确定性、先验敏感性与生物学解释的依据。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明;摘要未给出聚类性能指标或一般比较条件,不能将特定数据结果推广为普遍优势。

原文摘要

Genes are often regulated in living cells by proteins called transcription factors that bind directly to short segments of DNA in close proximity to specific genes. These binding sites have a conserved nucleotide appearance, which is called a motif. Several recent studies of transcriptional regulation require the reduction of a large collection of motifs into clusters based on the similarity of their nucleotide composition. We present a principled approach to this clustering problem based on a Bayesian hierarchical model that accounts for both within- and between-motif variability. We use a Dirichlet process prior distribution that allows the number of clusters to vary and we also present a novel generalization that allows the core width of each motif to vary. This clustering model is implemented, using a Gibbs sampling strategy, on several collections of transcription factor motif matrices. Our stochastic implementation allows us to examine the variability of our results in addition to focusing on a set of best clusters. Our clustering results identify several motif clusters that suggest that several transcription factor protein families are actually mixtures of several smaller groups of highly similar motifs, which provide substantially more refined information compared with the full set of motifs in the family. Our clusters provide a means by which to organize transcription factors based on binding motif similarities and can be used to reduce motif redundancy within large databases such as JASPAR and TRANSFAC, which aides the use of these databases for further motif discovery. Finally, our clustering procedure has been used in combination with discovery of evolutionarily conserved motifs to predict co-regulated genes. An alternative to our Dirichlet process prior distribution is presented that differs substantially in terms of a priori clustering characteristics, but shows no substantive difference in the clustering results for our dataset. Despite our specific application to transcription factor binding motifs, our Bayesian clustering model based on the Dirichlet process has several advantages over traditional clustering methods that could make our procedure appropriate and useful for many clustering applications.

笔记与分组
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