<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/GSE318nnn/GSE318105/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Homo sapiens</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE318105</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>CAD-C: An engineered nuclease enables repair-free in situ proximity ligation and nucleosome-resolution chromosome walks in human cells [CAD-Seq]</name><description>Chromosome conformation capture (3C)-derived methods have become an indispensable tool in the study of gene regulation. The three-dimensional contacts can probe depend strongly on the properties of the enzyme used to fragment chromatin prior to proximity-driven ligation. Micrococcal nuclease (MNase), used in Micro-C, increases resolution at the expense of low ligation efficiency and the need for extensive enzyme titration. To overcome these limitations, we engineered a highly active, TEV protease-activatable caspase-activated DNase (CAD) to enable an efficient, low-sequence-bias, and high-resolution proximity ligation assay we call CAD-C. CAD-C was successful on the first attempt for each human cell line tested and the resulting datasets capture loops, TADs, compartments, and stripes similarly to Micro-C. However, compared to Micro-C and Hi-C, CAD-C shows enhanced sensitivity for promoter-enhancer loops. Leveraging the ligation-competent DNA ends produced by CAD cleavage, we show that CAD-C is compatible with a highly streamlined, repair-free protocol and produces multi-step CADwalks, consecutive ligations between nucleosomal or sub-nucleosomal fragments. With these walks, we probe local chromatin fiber folding contacts, nucleosomal and sub-nucleosomal footprints, and long-range nuclear organization regimes in human cell lines. CAD-C is an efficient, robust chromatin structure assay that can span sub-nucleosomal to chromosomal length scales in a single experiment.</description><dates><publication>2026/08/07</publication></dates><accession>GSE318105</accession><cross_references><GSM>GSM9486242</GSM><GSM>GSM9486243</GSM><GSM>GSM9486240</GSM><GSM>GSM9486241</GSM><GSM>GSM9486248</GSM><GSM>GSM9486249</GSM><GSM>GSM9486246</GSM><GSM>GSM9486247</GSM><GSM>GSM9486244</GSM><GSM>GSM9486245</GSM><GSM>GSM9486253</GSM><GSM>GSM9486254</GSM><GSM>GSM9486251</GSM><GSM>GSM9486252</GSM><GSM>GSM9486250</GSM><GSM>GSM9486239</GSM><GSM>GSM9486237</GSM><GSM>GSM9486238</GSM><GSM>GSM9486257</GSM><GSM>GSM9486235</GSM><GSM>GSM9486236</GSM><GSM>GSM9486258</GSM><GSM>GSM9486255</GSM><GSM>GSM9486234</GSM><GSM>GSM9486256</GSM><GPL>34281</GPL><GSE>318105</GSE><taxon>Homo sapiens</taxon><PMID>[42146372]</PMID></cross_references></HashMap>