Banjo vape. Celiac pabst slow-carb

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{"type":"standard","title":"NOMe-seq","displaytitle":"NOMe-seq","namespace":{"id":0,"text":""},"wikibase_item":"Q120142918","titles":{"canonical":"NOMe-seq","normalized":"NOMe-seq","display":"NOMe-seq"},"pageid":73169871,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/c/c9/Figure_1_NOMe-seq_overview_final_1.jpg/330px-Figure_1_NOMe-seq_overview_final_1.jpg","width":320,"height":297},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/c/c9/Figure_1_NOMe-seq_overview_final_1.jpg","width":3261,"height":3027},"lang":"en","dir":"ltr","revision":"1289155694","tid":"c242f933-2ab8-11f0-bec7-ff9e1b4dba06","timestamp":"2025-05-06T20:29:07Z","description":"NOMe-seq is a nucleosome occupancy and methylome technique.","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/NOMe-seq","revisions":"https://en.wikipedia.org/wiki/NOMe-seq?action=history","edit":"https://en.wikipedia.org/wiki/NOMe-seq?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:NOMe-seq"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/NOMe-seq","revisions":"https://en.m.wikipedia.org/wiki/Special:History/NOMe-seq","edit":"https://en.m.wikipedia.org/wiki/NOMe-seq?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:NOMe-seq"}},"extract":"Nucleosome Occupancy and Methylome Sequencing (NOMe-seq) is a genomics technique used to simultaneously detect nucleosome positioning and DNA methylation. This method is an extension of bisulfite sequencing, considered the gold standard for profiling DNA methylation. NOMe-seq relies on the methyltransferase M.CviPl, which methylates cytosines in GpC dinucleotides unbound by nucleosomes or other proteins, creating a nucleosome footprint. The mammalian genome naturally contains DNA methylation, but only at CpG sites, so GpC methylation can be differentiated from genomic methylation after bisulfite sequencing. This allows simultaneous analysis of the nucleosome footprint and endogenous methylation on the same DNA molecules. In addition to nucleosome foot-printing, NOMe-seq can determine locations bound by transcription factors. Nucleosomes are bound by 147 base pairs of DNA whereas transcription factors or other proteins will only bind a region of approximately 10-80 base pairs. Following treatment with M.CviPl, nucleosome and transcription factor sites can be differentiated based on the size of the unmethylated GpC region.","extract_html":"

Nucleosome Occupancy and Methylome Sequencing (NOMe-seq) is a genomics technique used to simultaneously detect nucleosome positioning and DNA methylation. This method is an extension of bisulfite sequencing, considered the gold standard for profiling DNA methylation. NOMe-seq relies on the methyltransferase M.CviPl, which methylates cytosines in GpC dinucleotides unbound by nucleosomes or other proteins, creating a nucleosome footprint. The mammalian genome naturally contains DNA methylation, but only at CpG sites, so GpC methylation can be differentiated from genomic methylation after bisulfite sequencing. This allows simultaneous analysis of the nucleosome footprint and endogenous methylation on the same DNA molecules. In addition to nucleosome foot-printing, NOMe-seq can determine locations bound by transcription factors. Nucleosomes are bound by 147 base pairs of DNA whereas transcription factors or other proteins will only bind a region of approximately 10-80 base pairs. Following treatment with M.CviPl, nucleosome and transcription factor sites can be differentiated based on the size of the unmethylated GpC region.

"}

{"fact":"A commemorative tower was built in Scotland for a cat named Towser, who caught nearly 30,000 mice in her lifetime.","length":114}

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