<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE346nnn/GSE346229/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Saccharomyces cerevisiae</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE346229</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>ATAC-seq and MNase-seq Detect Distinct Modes of Chromatin Accessibility [ATAC-seq]</name><description>Chromatin accessibility shapes the ability of transcription factors (TFs) and the transcriptional machinery to engage genomic DNA and therefore plays a central role in gene regulation. Two widely used approaches for profiling chromatin accessibility are micrococcal nuclease (MNase)-seq and assay for transposase-accessible chromatin (ATAC)-seq. ATAC-seq peaks are often thought to be equivalent to nucleosome-depleted regions (NDRs) that are defined by MNase-seq; however, these two measurements have not been systematically compared. Here, we performed a side-by-side comparison of ATAC-seq and MNase-seq in budding yeast and found a substantial discrepancy between ATAC-seq peaks and MNase-defined NDRs. This discrepancy is not primarily explained by intrinsic differences between MNase and Tn5 enzymatic activity. Instead, ATAC-seq peaks and NDRs capture distinct chromatin states. Specifically, ATAC-seq peaks are enriched at dynamic nucleosomes associated with transcriptional co-regulators, including SAGA and SWI/SNF, whereas NDRs mark more static nucleosome-free regions at promoters. Depletion of SWI/SNF, but not RSC, reduces ATAC-seq signals. Generation of NDRs and ATAC-seq peaks requires distinct TF properties, and native TFs differ in their ability to produce these two types of open chromatin. Finally, we show that the functional distinction between ATAC-seq peaks and NDRs are widespread across eukaryotic species, including human cells. Together, our results provide new insights into the biological meaning of chromatin accessibility measured by these two assays.</description><dates><publication>2026/09/08</publication></dates><accession>GSE346229</accession><cross_references><GSM>GSM10029266</GSM><GSM>GSM10029288</GSM><GSM>GSM10029265</GSM><GSM>GSM10029287</GSM><GSM>GSM10029264</GSM><GSM>GSM10029286</GSM><GSM>GSM10029285</GSM><GSM>GSM10029263</GSM><GSM>GSM10029269</GSM><GSM>GSM10029268</GSM><GSM>GSM10029267</GSM><GSM>GSM10029280</GSM><GSM>GSM10029262</GSM><GSM>GSM10029284</GSM><GSM>GSM10029261</GSM><GSM>GSM10029283</GSM><GSM>GSM10029282</GSM><GSM>GSM10029260</GSM><GSM>GSM10029281</GSM><GSM>GSM10029255</GSM><GSM>GSM10029277</GSM><GSM>GSM10029276</GSM><GSM>GSM10029254</GSM><GSM>GSM10029275</GSM><GSM>GSM10029274</GSM><GSM>GSM10029259</GSM><GSM>GSM10029258</GSM><GSM>GSM10029279</GSM><GSM>GSM10029257</GSM><GSM>GSM10029256</GSM><GSM>GSM10029278</GSM><GSM>GSM10029273</GSM><GSM>GSM10029272</GSM><GSM>GSM10029271</GSM><GSM>GSM10029270</GSM><GPL>31112</GPL><GSE>346229</GSE><taxon>Saccharomyces cerevisiae</taxon></cross_references></HashMap>