<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Wenqing Shui</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0016563000</full_dataset_link><submitter_email>shuiwq@shanghaitech.edu.cn</submitter_email><submitter_affiliation>ShanghaiTech University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>LiP-MS data analysis workflows with a hybrid LiP proteome benchmark</name><description>To evaluate informatics workflows for DIA-based LiP-MS, we generated a high-quality benchmark data set comprising more than 170,000 LiP peptides with defined composition. We then performed comprehensive assessment of major DIA analysis platforms incorporating different spectral libraries, and introduced DIA-LiPQuan, an informatics pipeline tailored to DIA LiP-MS quantification and downstream analysis. Data re-analysis by DIA-LiPQuan with in silico libraries allows sensitive and robust detection of both site-specific structural remodeling of proteins and drug-bound protein targets from the cellular proteome. Collectively, our study provides a valuable benchmark resource and informatics package for LiP-MS data mining, which would facilitate its broader applications in structural proteomics and drug discovery.</description><dates><publication>Tue Apr 14 00:00:00 BST 2026</publication></dates><accession>PXD077171</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>