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Variants of this formalism have been developed to enable different coupling types between the same cells to be included.
These subtle differences could also reflect technical variation between the same cells, RNA prepared, amplified, and hybridized in parallel 8. Thus, in cells isolated by CD4 MACS and FACS neither the degradation of RNA, nor the de novo transcription ex vivo skewed the in vivo transcriptomes.
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Proteins differ greatly between two cells, between the same cell at different times and between normal and abnormal cells.
Cells with the Hm preference move so that they penetrate between the same cell types as themselves.
Such data highlight both the unsuitability of these genes as bovine NP cell markers and the considerable differences that can be observed between the same cell types in different species.
In contrast, monomers affect the function of dimers by occupying cell surface molecules and conjugates of three or more IgGs may lead to ineffective contact between the same cell populations.
In particular, using ENCODE ChIP-Seq data for H3K36me3 and RNAPII from the cell lines K562 and NHEK, we obtain a high correlation for the Z-scores of these signals when compared with the enrichment Z-scores for RNA-Seq between the same cell lines.
The GC content distributions differ between TFs profiled in the same cells and between different cell types profiled for the same TF (Additional file 2: Figure S1).
Here, we consider three gaps as follows: gaps between 1) the same cell types, 2) the same cell type and different cell type, and 3) the same cell type and cavity (Fig. 3).
Homotypic repulsive interactions have been shown to act not only between branches of the same cell but also between neighboring cells of the same type.
Terms associated with individual metaclusters were considerably more different between metaclusters in the same cell line than between metaclusters in different cell lines [Additional file 1: Figure S8].
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