<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Y</submitter><funding>NIBIB NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institute of Biomedical Imaging and Bioengineering</funding><funding>NIH HHS</funding><pagination>15161</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9452525</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>Cryo-imaging provided 3D whole-mouse microscopic color anatomy and fluorescence images that enables biotechnology applications (e.g., stem cells and metastatic cancer). In this report, we compared three methods of organ segmentation: 2D U-Net with 2D-slices and 3D U-Net with either 3D-whole-mouse or 3D-patches. We evaluated the brain, thymus, lung, heart, liver, stomach, spleen, left and right kidney, and bladder. Training with 63 mice, 2D-slices had the best performance, with median Dice scores of &amp;gt; 0.9 and median Hausdorff distances of &amp;lt; 1.2 mm in eightfold cross validation for all organs, except bladder, which is a problem organ due to variable filling and poor contrast. Results were comparable to those for a second analyst on the same data. Regression analyses were performed to fit learning curves, which showed that 2D-slices can succeed with fewer samples. Review and editing of 2D-slices segmentation results reduced human operator time from ~ 2-h to ~ 25-min, with reduced inter-observer variability. As demonstrations, we used organ segmentation to evaluate size changes in liver disease and to quantify the distribution of therapeutic mesenchymal stem cells in organs. With a 48-GB GPU, we determined that extra GPU RAM improved the performance of 3D deep learning because we could train at a higher resolution.</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Deep learning multi-organ segmentation for whole mouse cryo-images including a comparison of 2D and 3D deep networks.</pubmed_title><pmcid>PMC9452525</pmcid><funding_grant_id>R44CA213601</funding_grant_id><funding_grant_id>R01 EB028635</funding_grant_id><funding_grant_id>C06 RR012463</funding_grant_id><funding_grant_id>R44 CA213601</funding_grant_id><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Gargesha M</pubmed_authors><pubmed_authors>Scott B</pubmed_authors><pubmed_authors>Wilson DL</pubmed_authors><pubmed_authors>Tchilibou Wane AO</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deep learning multi-organ segmentation for whole mouse cryo-images including a comparison of 2D and 3D deep networks.</name><description>Cryo-imaging provided 3D whole-mouse microscopic color anatomy and fluorescence images that enables biotechnology applications (e.g., stem cells and metastatic cancer). In this report, we compared three methods of organ segmentation: 2D U-Net with 2D-slices and 3D U-Net with either 3D-whole-mouse or 3D-patches. We evaluated the brain, thymus, lung, heart, liver, stomach, spleen, left and right kidney, and bladder. Training with 63 mice, 2D-slices had the best performance, with median Dice scores of &amp;gt; 0.9 and median Hausdorff distances of &amp;lt; 1.2 mm in eightfold cross validation for all organs, except bladder, which is a problem organ due to variable filling and poor contrast. Results were comparable to those for a second analyst on the same data. Regression analyses were performed to fit learning curves, which showed that 2D-slices can succeed with fewer samples. Review and editing of 2D-slices segmentation results reduced human operator time from ~ 2-h to ~ 25-min, with reduced inter-observer variability. As demonstrations, we used organ segmentation to evaluate size changes in liver disease and to quantify the distribution of therapeutic mesenchymal stem cells in organs. With a 48-GB GPU, we determined that extra GPU RAM improved the performance of 3D deep learning because we could train at a higher resolution.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-18T18:24:37.385Z</modification><creation>2025-04-07T06:02:39.995Z</creation></dates><accession>S-EPMC9452525</accession><cross_references><pubmed>36071089</pubmed><doi>10.1038/s41598-022-19037-3</doi></cross_references></HashMap>