<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Chao Liu</submitter><species>Homo Sapiens</species><species>Saccharomyces Cerevisiae</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0016059000</full_dataset_link><submitter_email>liuchaobuaa@buaa.edu.cn</submitter_email><submitter_affiliation>Beihang University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Ultra-sensitive cohort data analysis for Orbitrap Astral based single-cell proteomics</name><description>Orbitrap Astral mass spectrometry driven data-independent acquisition (DIA) strategy enables deep profiling in shotgun proteomics and is increasingly adopted in single-cell proteomics (SCP). However, the high proportion of missing values reported by existing DIA software remains a bottleneck for sensitive SCP analysis. Here, we present ApuQuant, an Orbitrap Astral DIA data analysis software that performs cohort-level re-identification and quantification. In ApuQuant, we apply a contrastive learning model to Match Between Run (MBR) analysis and introduce a false discovery rate estimation algorithm to rule out false MBR results across runs within a cohort. Compared with DIA-NN and Spectronaut, ApuQuant reduced missing values from 43.45%–50.82% to nearly 1% on a technical-replicate dataset, thereby enabling ultra-sensitive data analysis. Further validation on additional datasets demonstrated that this improvement was achieved without increasing false positive results. Finally, ApuQuant was applied to an A549-single-cell proteomics dataset and showed a 39.99% increase in protein identifications, illustrating a more comprehensive characterization of proteomic heterogeneity at single-cell resolution.</description><dates><publication>Thu Apr 23 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD077556</accession><cross_references><TAXONOMY>9606</TAXONOMY><TAXONOMY>4932</TAXONOMY></cross_references></HashMap>