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ATAC-seq profiles the gene regulatory ‘landscape’ of a cell. Promoters, enhancers and other putative gene regulatory elements are identified as peaks in the data and these signals are highly cell-type-specific. Here, the skylines of Paris, San Francisco, New York City and Shanghai are depicted in the style of cell-type-specific ATAC-seq peaks.
This Protocol Extension (to an existing SELEX Nature Protocol) introduces RNA G-quadruplex (rG4)-SELEX, a method that generates novel l-RNA aptamers to target rG4 structures that can be applied to inhibit G-quadruplex-mediated interactions.
This protocol provides steps for DNA amplicon sequencing using miniaturized laboratory equipment for rapid in situ identification of biological specimens in environments such as local institutions, field stations and classrooms.
This protocol describes enrichment of telomeric repeats from human and mouse cells by successive rounds of restriction digestion and size fractionation, resulting in high-quality preparations suitable for single-molecule and structural studies.
This protocol combines in situ chromosome conformation capture with labeling of nascent DNA with the synthetic nucleoside 4-thio-thymidine to generate genome-wide contact probability maps within and across sister chromatids in mammalian cells.
A protocol for generating chromatin accessibility profiles from a broad variety of cell and tissue types, including a step-by-step workflow for library preparation and guidelines for data processing and downstream analysis.