five

RNAseq for WT and oschz1 mutant

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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE155268
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At genome-wide level, loss of OsChz1 causes mis-regulation of thousands of genes and broad alterations of nucleosome occupancy as well as reduction of H2A.Z-enrichment within chromatin along the gene body and at TSS. While OsChz1 associates with chromatin regions enriched of repressive histone marks (H3K27me3 and H4K4me2), its loss does not affect the genome landscape of DNA methylation. 2 geneotype with 3 replicates
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2020-11-24
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