<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/GSE318343/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE318343</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>PCRD-seq: Proximity Crosslinking-induced RNA Depletion for Low-Input Chromatin-associated Transcriptome Profiling</name><description>Chromatin-associated RNAs play critical roles in regulating chromatin organization and transcription, underscoring the importance of their study. Proximity labeling has emerged as a promising and versatile technique for profiling chromatin-associated RNAs with high spatiotemporal resolution. While being a powerful technique, traditional proximity labeling methods depend on complex, high-input enrichment protocols, which significantly limit their wide practical application. Here, we developed a straightforward, enrichment-free chromatin-associated RNA profiling strategy: Proximity Crosslinking-induced RNA Depletion sequencing (PCRD-seq). This approach leverages the proximity crosslinking between chromatin and its surrounding RNAs induced by singlet oxygen generated by HoeDBF, a photosensitizer targeting chromatin region. The proximity crosslinking hinders the release of chromatin-associated RNAs during routine TRIzol extraction, consequently leading to a specific depletion of these RNAs. This method was successfully applied to investigate the role of U1 snRNA in RNA chromatin retention and the differences in chromatin-associated transcriptomes between two ovarian cancer cell lines with opposite metastatic capability. Moreover, our PCRD-seq exhibits potential in profiling nuclear lamina-associated RNAs, which paves the way for its application to profile RNAs associated with other chromatin subdomains. The minimal cell input and simple workflow endow PCRD-seq as a transformative tool for wide applications.</description><dates><publication>2026/09/16</publication></dates><accession>GSE318343</accession><cross_references><GSM>GSM9492821</GSM><GSM>GSM9492788</GSM><GSM>GSM9492789</GSM><GSM>GSM9492822</GSM><GSM>GSM9492786</GSM><GSM>GSM9492787</GSM><GSM>GSM9492820</GSM><GSM>GSM9492825</GSM><GSM>GSM9492826</GSM><GSM>GSM9492823</GSM><GSM>GSM9492824</GSM><GSM>GSM9492829</GSM><GSM>GSM9492827</GSM><GSM>GSM9492828</GSM><GSM>GSM9492791</GSM><GSM>GSM9492792</GSM><GSM>GSM9492790</GSM><GSM>GSM9492795</GSM><GSM>GSM9492796</GSM><GSM>GSM9492793</GSM><GSM>GSM9492794</GSM><GSM>GSM9492832</GSM><GSM>GSM9492799</GSM><GSM>GSM9492833</GSM><GSM>GSM9492830</GSM><GSM>GSM9492797</GSM><GSM>GSM9492831</GSM><GSM>GSM9492798</GSM><GSM>GSM9492836</GSM><GSM>GSM9492837</GSM><GSM>GSM9492834</GSM><GSM>GSM9492835</GSM><GSM>GSM9492838</GSM><GSM>GSM9492839</GSM><GSM>GSM9492840</GSM><GSM>GSM9492766</GSM><GSM>GSM9492843</GSM><GSM>GSM9492844</GSM><GSM>GSM9492767</GSM><GSM>GSM9492800</GSM><GSM>GSM9492841</GSM><GSM>GSM9492842</GSM><GSM>GSM9492847</GSM><GSM>GSM9492803</GSM><GSM>GSM9492804</GSM><GSM>GSM9492848</GSM><GSM>GSM9492801</GSM><GSM>GSM9492768</GSM><GSM>GSM9492845</GSM><GSM>GSM9492769</GSM><GSM>GSM9492846</GSM><GSM>GSM9492802</GSM><GSM>GSM9492807</GSM><GSM>GSM9492808</GSM><GSM>GSM9492849</GSM><GSM>GSM9492805</GSM><GSM>GSM9492806</GSM><GSM>GSM9492809</GSM><GSM>GSM9492770</GSM><GSM>GSM9492773</GSM><GSM>GSM9492850</GSM><GSM>GSM9492774</GSM><GSM>GSM9492851</GSM><GSM>GSM9492771</GSM><GSM>GSM9492772</GSM><GSM>GSM9492810</GSM><GSM>GSM9492777</GSM><GSM>GSM9492778</GSM><GSM>GSM9492811</GSM><GSM>GSM9492852</GSM><GSM>GSM9492775</GSM><GSM>GSM9492776</GSM><GSM>GSM9492814</GSM><GSM>GSM9492815</GSM><GSM>GSM9492812</GSM><GSM>GSM9492779</GSM><GSM>GSM9492813</GSM><GSM>GSM9492818</GSM><GSM>GSM9492819</GSM><GSM>GSM9492816</GSM><GSM>GSM9492817</GSM><GSM>GSM9492780</GSM><GSM>GSM9492781</GSM><GSM>GSM9492784</GSM><GSM>GSM9492785</GSM><GSM>GSM9492782</GSM><GSM>GSM9492783</GSM><GPL>20795</GPL><GPL>24676</GPL><GPL>34284</GPL><GSE>318343</GSE><taxon>Homo sapiens</taxon><PMID>[42644390]</PMID></cross_references></HashMap>