{"database":"iProX","file_versions":[],"scores":null,"additional":{"omics_type":["Proteomics"],"submitter":["Chao Liu"],"species":["Homo Sapiens","Saccharomyces Cerevisiae"],"full_dataset_link":["http://www.iprox.org/page/project.html?id=IPX0016059000"],"submitter_email":["liuchaobuaa@buaa.edu.cn"],"submitter_affiliation":["Beihang University"],"sample_protocol":[""],"repository":["iProX"],"data_protocol":[""],"additional_accession":[]},"is_claimable":false,"name":"Ultra-sensitive cohort data analysis for Orbitrap Astral based single-cell proteomics","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.","dates":{"publication":"Thu Apr 23 00:00:00 GMT+01:00 2026"},"accession":"PXD077556","cross_references":{"TAXONOMY":["9606","4932"]}}