ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR604/000/SRR6042840/SRR6042840.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR604/004/SRR6042834/SRR6042834.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR604/008/SRR6042838/SRR6042838.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR604/000/SRR6042830/SRR6042830.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR604/002/SRR6042832/SRR6042832.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR604/006/SRR6042836/SRR6042836.fastq.gzprimaryOK200GenomicsSelker, Biology, Institute of Molecular Biology, University of Oregonhttps://www.ebi.ac.uk/ena/browser/view/PRJNA407574Neurospora crassaxref:PubMed:29078403Purpose: The goal of this study is to characterize the domain(s) of H3K9me3 induced by artifical localization of heterochromatin factors in wild-type and mutant backgrounds. Overall design: Methods: ChIP-seq was performed on each sample (H3K9me3 ChIP six samples total). qRT-PCR validation was done with SYBR Green reagent.ENAfalseNeurospora crassaGenome-wide maps of H3K9me3 with tethered heterochromatin machinery2025-09-242017-09-17PRJNA407574GSE103926514129078403