<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang S</submitter><funding>Guizhou Provincial People's Hospital National Science Foundation</funding><funding>Guizhou Provincial People's Hospital Doctor Foundation</funding><funding>Guizhou Provincial Science and Technology Projects</funding><funding>National Natural Science Foundation of China</funding><funding>General Project of Chongqing Natural Science Foundation</funding><funding>Guizhou Provincial People's Hospital Youth Fund</funding><pagination>e18296</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11069052</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(9)</volume><pubmed_abstract>We investigated subarachnoid haemorrhage (SAH) macrophage subpopulations and identified relevant key genes for improving diagnostic and therapeutic strategies. SAH rat models were established, and brain tissue samples underwent single-cell transcriptome sequencing and bulk RNA-seq. Using single-cell data, distinct macrophage subpopulations, including a unique SAH subset, were identified. The hdWGCNA method revealed 160 key macrophage-related genes. Univariate analysis and lasso regression selected 10 genes for constructing a diagnostic model. Machine learning algorithms facilitated model development. Cellular infiltration was assessed using the MCPcounter algorithm, and a heatmap integrated cell abundance and gene expression. A 3 × 3 convolutional neural network created an additional diagn</pubmed_abstract><journal>Journal of cellular and molecular medicine</journal><pubmed_title>Machine learning and deep learning to identifying subarachnoid haemorrhage macrophage-associated biomarkers by bulk and single-cell sequencing.</pubmed_title><pmcid>PMC11069052</pmcid><funding_grant_id>GPPH-NSFC-2019-09</funding_grant_id><funding_grant_id>82260533</funding_grant_id><funding_grant_id>[2018]03</funding_grant_id><funding_grant_id>CSTB2023NSCQ-MSX0749</funding_grant_id><funding_grant_id>[2018]06</funding_grant_id><funding_grant_id>82360482</funding_grant_id><funding_grant_id>[2020]1Z066</funding_grant_id><funding_grant_id>GPPH-NSFC-2019-18</funding_grant_id><funding_grant_id>GPPH-NSFC-D-2019-17</funding_grant_id><funding_grant_id>GZSYQN202202</funding_grant_id><funding_grant_id>82360376</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Ran Z</pubmed_authors><pubmed_authors>Deng M</pubmed_authors><pubmed_authors>Hao Y</pubmed_authors><pubmed_authors>Tan Y</pubmed_authors><pubmed_authors>Han G</pubmed_authors><pubmed_authors>Ma J</pubmed_authors><pubmed_authors>Xiang X</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Shi H</pubmed_authors><pubmed_authors>Luo T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Machine learning and deep learning to identifying subarachnoid haemorrhage macrophage-associated biomarkers by bulk and single-cell sequencing.</name><description>We investigated subarachnoid haemorrhage (SAH) macrophage subpopulations and identified relevant key genes for improving diagnostic and therapeutic strategies. SAH rat models were established, and brain tissue samples underwent single-cell transcriptome sequencing and bulk RNA-seq. Using single-cell data, distinct macrophage subpopulations, including a unique SAH subset, were identified. The hdWGCNA method revealed 160 key macrophage-related genes. Univariate analysis and lasso regression selected 10 genes for constructing a diagnostic model. Machine learning algorithms facilitated model development. Cellular infiltration was assessed using the MCPcounter algorithm, and a heatmap integrated cell abundance and gene expression. A 3 × 3 convolutional neural network created an additional diagn</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-07-14T18:58:47.895Z</modification><creation>2026-06-22T03:13:04.671Z</creation></dates><accession>S-EPMC11069052</accession><cross_references><pubmed>38702954</pubmed><doi>10.1111/jcmm.18296</doi></cross_references></HashMap>