{"conceptdoi":"10.14278/rodare.3000","conceptrecid":"3000","created":"2024-06-05T20:10:47.793695+00:00","doi":"10.14278/rodare.3001","files":[{"bucket":"fae71336-c6d2-45b2-ae65-416c8f57b5a0","checksum":"md5:8d00f9b3bbcd8653d12439dc797ba497","key":"HeLaCytoNuc_raw_images.zip","links":{"self":"https://rodare.hzdr.de/api/files/fae71336-c6d2-45b2-ae65-416c8f57b5a0/HeLaCytoNuc_raw_images.zip"},"size":8595625573,"type":"zip"},{"bucket":"fae71336-c6d2-45b2-ae65-416c8f57b5a0","checksum":"md5:7324a5d360fef7dacd6d625384aadc4a","key":"HeLaCytoNuc_test_cellprofiler_masks.zip","links":{"self":"https://rodare.hzdr.de/api/files/fae71336-c6d2-45b2-ae65-416c8f57b5a0/HeLaCytoNuc_test_cellprofiler_masks.zip"},"size":3666113,"type":"zip"},{"bucket":"fae71336-c6d2-45b2-ae65-416c8f57b5a0","checksum":"md5:de45497da77317486f6ed51224a8e3d5","key":"HeLaCytoNuc_test.zip","links":{"self":"https://rodare.hzdr.de/api/files/fae71336-c6d2-45b2-ae65-416c8f57b5a0/HeLaCytoNuc_test.zip"},"size":76153291,"type":"zip"},{"bucket":"fae71336-c6d2-45b2-ae65-416c8f57b5a0","checksum":"md5:ca89238d7be977939ca0a67b94306891","key":"HeLaCytoNuc_train.zip","links":{"self":"https://rodare.hzdr.de/api/files/fae71336-c6d2-45b2-ae65-416c8f57b5a0/HeLaCytoNuc_train.zip"},"size":434887789,"type":"zip"},{"bucket":"fae71336-c6d2-45b2-ae65-416c8f57b5a0","checksum":"md5:bb684299f81dfb2e12f47ae8e5bbfbcd","key":"HeLaCytoNuc_validation.zip","links":{"self":"https://rodare.hzdr.de/api/files/fae71336-c6d2-45b2-ae65-416c8f57b5a0/HeLaCytoNuc_validation.zip"},"size":139881304,"type":"zip"}],"id":3001,"links":{"badge":"https://rodare.hzdr.de/badge/doi/10.14278/rodare.3001.svg","bucket":"https://rodare.hzdr.de/api/files/fae71336-c6d2-45b2-ae65-416c8f57b5a0","conceptbadge":"https://rodare.hzdr.de/badge/doi/10.14278/rodare.3000.svg","conceptdoi":"https://doi.org/10.14278/rodare.3000","doi":"https://doi.org/10.14278/rodare.3001","html":"https://rodare.hzdr.de/record/3001","latest":"https://rodare.hzdr.de/api/records/3001","latest_html":"https://rodare.hzdr.de/record/3001","self":"https://rodare.hzdr.de/api/records/3001"},"metadata":{"access_right":"open","access_right_category":"success","communities":[{"id":"health"},{"id":"rodare"}],"creators":[{"affiliation":"Center for Advanced Systems Understanding, Helmholtz-Zentrum Dresden-Rossendorf","name":"De, Trina","orcid":"0000-0003-1111-9851"},{"affiliation":"Center for Advanced Systems Understanding, Helmholtz-Zentrum Dresden-Rossendorf","name":"Urbanski, Adrian","orcid":"0009-0008-6619-3665"},{"affiliation":"Center for Advanced Systems Understanding, Helmholtz-Zentrum Dresden-Rossendorf","name":"Thangamani, Subasini"},{"affiliation":"Center for Advanced Systems Understanding, Helmholtz-Zentrum Dresden-Rossendorf","name":"Wyrzykowska, Maria"},{"affiliation":"Center for Advanced Systems Understanding, Helmholtz-Zentrum Dresden-Rossendorf","name":"Yakimovich, Artur","orcid":"0000-0003-2458-4904"}],"description":"<p><strong>Data Description:</strong></p>\n\n<p>This dataset comprises fluorescence micrographs of HeLa cells, specifically labelled to identify nuclei and cell cytoplasm. These images were acquired as a technical calibration for a high-content screening study detailed and published in [1].</p>\n\n<p>The HeLa cell line (ATCC-CCL-2), a widely used immortalised cell line in laboratory research, was cultured under standard conditions. Post-cultivation, the cells were fixed and stained with fluorescent dyes to visualise the nuclei and cytoplasm. The nuclei were stained with DAPI (4&#39;,6-diamidino-2-phenylindole), a blue-fluorescent DNA stain, while fluorescent-labeled phalloidin was used to detect actin filaments and delineate the cytoplasm. The entire process of cell culture, fixation, staining, and imaging adhered strictly to the protocols described in [1].</p>\n\n<p>The preprocessed dataset includes 2,676 8-bit RGB images, each with a pixel resolution of 520 x 696 pixels. In these images, only two of the RGB channels are utilized: the red channel represents the cytoplasm, and the blue channel represents the nuclei. The dataset is divided into training, validation, and test subsets in a 70:20:10 ratio. The entire dataset is accompanied by instance segmentation masks for nuclei and cytoplasm objects obtained through a specialised CellProfiler [2] software. Notably, the test subset was annotated manually by a specialist, ensuring high-quality annotations. The original raw images are of a higher resolution, 1040 x 1392 pixels, and have a bit depth of 16 bits, providing more detailed information for advanced analyses.</p>\n\n<p><br>\n<strong>File&nbsp;Description:</strong></p>\n\n<p>The file structure of the zip files is as follows:</p>\n\n\n\n<p>HeLaCytoNuc_{train/validation/test}.zip -&gt;</p>\n\n<p>- images -&gt; {filename}.tif</p>\n\n<p>- nuclei_masks&nbsp; -&gt; {filename}.tif</p>\n\n<p>- cytoplasm_masks&nbsp; -&gt; {filename}.tif</p>\n\n\n\n<p>HeLaCytoNuc_raw_images.zip -&gt; {filename}.tif</p>\n\n\n\n<p>HeLaCytoNuc_test_cellprofiler_masks.zip -&gt;</p>\n\n<p>- nuclei_masks&nbsp; -&gt; {filename}.tif</p>\n\n<p>- cytoplasm_masks&nbsp; -&gt; {filename}.tif&nbsp;</p>\n\n\n\n<p><strong>References:</strong></p>\n\n<p>1.&nbsp;R&auml;m&ouml;, Pauli, Anna Drewek, C&eacute;cile Arrieumerlou, Niko Beerenwinkel, Houchaima Ben-Tekaya, Bettina Cardel, Alain Casanova et al. &quot;Simultaneous analysis of large-scale RNAi screens for pathogen entry.&quot;&nbsp;<em>BMC genomics</em>&nbsp;15 (2014): 1-18.</p>\n\n<p>2.&nbsp;Carpenter, Anne E., Thouis R. Jones, Michael R. Lamprecht, Colin Clarke, In Han Kang, Ola Friman, David A. Guertin et al. &quot;CellProfiler: image analysis software for identifying and quantifying cell phenotypes.&quot;&nbsp;<em>Genome biology</em>&nbsp;7 (2006): 1-11.</p>","doc_id":"1","doi":"10.14278/rodare.3001","keywords":["Fluorescence microscopy","high content microscopy","cytoskeleton","cell nuclei"],"language":"eng","license":{"id":"CC-BY-4.0"},"pub_id":"39181","publication_date":"2024-06-05","related_identifiers":[{"identifier":"https://www.hzdr.de/publications/Publ-39181","relation":"isIdenticalTo","scheme":"url"},{"identifier":"10.14278/rodare.3000","relation":"isVersionOf","scheme":"doi"}],"relations":{"version":[{"count":1,"index":0,"is_last":true,"last_child":{"pid_type":"recid","pid_value":"3001"},"parent":{"pid_type":"recid","pid_value":"3000"}}]},"resource_type":{"title":"Dataset","type":"dataset"},"title":"HeLaCytoNuc: fluorescence microscopy dataset with segmentation masks for cell nuclei and cytoplasm","version":"Version 1"},"owners":[506],"revision":5,"stats":{"downloads":892.0,"unique_downloads":620.0,"unique_views":1440.0,"version_downloads":892.0,"version_unique_downloads":620.0,"version_unique_views":1440.0,"version_views":1561.0,"version_volume":1216552671035.0,"views":1561.0,"volume":1216552671035.0},"updated":"2024-06-06T08:03:15.641958+00:00"}