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In addition, we determined statistical enrichment of transcription factors` individual regulons at every time point (Supplementary Table 3). To this end, we restricted the list of differentially expressed genes, constructed as described above, to only those genes whose regulation was described in RegulonDB and a recently published set of regulatory connections (Faith et al., 2007). For each transcription factor both databases, we calculated the likelihood of finding the given number of its targets in this reduced query set using hypergeometric distribution, under the assumption that each transcription factor`s regulon was correctly and completely described by RegulonDB and the regulation map. Finally, as a separate analysis of differential gene expression, we conflated difference of z-scores across all time points by utilizing the formula, Zaverage Phenotypic analysis of deletion mutants To identify potential gyrase inhibitor-mediated genetic responses that contribute to cellular death in E. coli
In addition, we determined statistical enrichment of transcription factors` individual regulons at every time point (Supplementary Table 3). To this end, we restricted the list of differentially expressed genes, constructed as described above, to only those genes whose regulation was described in RegulonDB and a recently published set of regulatory connections (Faith et al., 2007). For each transcription factor both databases, we calculated the likelihood of finding the given number of its targets in this reduced query set using hypergeometric distribution, under the assumption that each transcription factor`s regulon was correctly and completely described by RegulonDB and the regulation map. Finally, as a separate analysis of differential gene expression, we conflated difference of z-scores across all time points by utilizing the formula, Zaverage Phenotypic analysis of deletion mutants To identify potential gyrase inhibitor-mediated genetic responses that contribute to cellular death in E. coli
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1012/5000

此外,我们在每个时间点确定了转录因子‘单个调节子’的统计富集(补充表3)。为此,我们将如上所述构建的差异表达基因的列表限制为那些其调控在RegulonDB和最近发表的一组调控连接中描述的基因(Faith等人,2007)。对于两个数据库中的每个转录因子,我们使用超几何分布计算了在这个缩减的查询集中找到其给定数量的靶的可能性,假设每个转录因子的调节子都由调节数据库和调节图正确和完整地描述。最后,作为对差异基因表达的单独分析,我们利用公式Zaverage合并了所有时间点的z值差异 缺失突变体的表型分析 确定促旋酶抑制剂介导的潜在遗传反应导致的细胞死亡 E.大肠杆菌

此外,我们在每个时间点确定了转录因子‘单个调节子’的统计富集(补充表3)。为此,我们将如上所述构建的差异表达基因的列表限制为那些其调控在RegulonDB和最近发表的一组调控连接中描述的基因(Faith等人,2007)。对于两个数据库中的每个转录因子,我们使用超几何分布计算了在这个缩减的查询集中找到其给定数量的靶的可能性,假设每个转录因子的调节子都由调节数据库和调节图正确和完整地描述。最后,作为对差异基因表达的单独分析,我们利用公式Zaverage合并了所有时间点的z值差异 缺失突变体的表型分析 确定促旋酶抑制剂介导的潜在遗传反应导致的细胞死亡 E.大肠杆菌

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