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The strength of selection that acts on a growing population of cells and the presence of a stochastic switching mechanism may be inferred from lineage data.
Application of single-molecule methods to assay genome-wide mRNA and protein levels in single bacteria provides a systems-level view of their relationship.
Analysis of RNA sequencing data points to fewer intergenic transcripts than assumed. Isolating them via chromatin association may enrich for functional noncoding transcripts.
To site-specifically label proteins in living cells, researchers mutate an enzyme to recognize a small fluorophore and catalyze its attachment to a small peptide tag.