The phrase "a set of enhancers" is correct and usable in written English.
It can be used when referring to multiple items or elements that enhance or improve something, such as a product, process, or experience.
Example: "The new software update includes a set of enhancers that improve the user interface and overall performance."
Alternatives: "a collection of enhancers" or "a group of enhancers".
Instead, we delineate a set of enhancers that gain accessibility in a CEBPA-dependent manner, suggesting a pioneering function of CEBPA.
These enhancers, defined using DNase I hypersensitive sites and histone marks, include a set of enhancers that is common to both fetal and adult erythroblasts, as well as developmental lineage-specific enhancers [ 20].
These ZPA- and AER-specific regions represent a set of enhancers active in regions that determine limb growth and patterning and can help inform our understanding of tetrapod limb development, evolutionary differences in limb morphology and the genetic etiology of human limb malformations.
A set of enhancer constructs generated for this study will be valuable reagents in identifying important trans-acting factor-binding sites and chromatin regulation during myoblast fusion.
A set of putative enhancers was defined based on the in vivo binding locations for early transcription, as measured previously by us using ChIP chip (MacArthur et al., 2009).
It has been shown that an enhancer deletion affects the expression of both H19 and Insulin-like growth factor 2 (Igf2), thus the Igf2 and the H19 genes are proposed to utilize a set of common enhancers [ 48, 49].
In contrast, the C. elegans study, which uses a simple polyQ tract attached to YFP (as opposed to using a polyQ tract and its surrounding CC region), reports a set of aggregation enhancers without enrichment in CC (Table 1).
Considering the union of H3K4me1 regions identified in eight cell lines as a set of likely enhancers, we observe again that sites predicted by all three methods overlap the most often with H3K4me1 regions, but that those predicted only by our SVM also overlap H3K4me1 marks significantly more often than those predicted only by one of the other two methods.
Following [ 35] we extracted a set of TSS-enhancer connections based on synchronized DHS activity during the transcription of a gene.
Perhaps when both MEIS1 and NKX2-5 acommone a common set of enhancers, MEIS1 establishes a ground state that maintains competence for eventual activation by NKX2-5 athehe appropriate stage of cardiac differentiation.
Only an in depth analysis of transcriptional levels of a large set of enhancers and conserved regions (highly conserved as well as ultraconserved) performed on nuclear and cytoplasmic RNA is likely to provide further clues with regards to the role of transcription in UCEs.
