TY - JOUR A1 - Dai, Chengxin A1 - Füllgrabe, Anja A1 - Pfeuffer, Julianus A1 - Solovyeva, Elizaveta M. A1 - Deng, Jingwen A1 - Moreno, Pablo A1 - Kamatchinathan, Selvakumar A1 - Kundu, Deepti Jaiswal A1 - George, Nancy A1 - Fexovy, Silvie A1 - Grüning, Björn A1 - Föll, Melanie Christine A1 - Griss, Johannes A1 - Vaudel, Marc A1 - Audain, Enrique A1 - Locard-Paulet, Marie A1 - Turewicz, Michael A1 - Eisenacher, Martin A1 - Uszkoreit, Julian A1 - Van Den Bossche, Tim A1 - Schwämmle, Veit A1 - Webel, Henry A1 - Schulze, Stefan A1 - Bouyssié, David A1 - Jayaram, Savita A1 - Duggineni, Vinay Kumar A1 - Samaras, Patroklos A1 - Wilhelm, Mathias A1 - Choi, Meena A1 - Wang, Mingxun A1 - Kohlbacher, Oliver A1 - Brazma, Alvis A1 - Papatheodorou, Irene A1 - Bandeira, Nuno A1 - Deutsch, Eric W. A1 - Vizcaíno, Juan Antonio A1 - Bai, Mingze A1 - Sachsenberg, Timo A1 - Levitsky, Lev I. A1 - Perez-Riverol, Yasset T1 - A proteomics sample metadata representation for multiomics integration and big data analysis JF - Nature Communications N2 - The amount of public proteomics data is rapidly increasing but there is no standardized format to describe the sample metadata and their relationship with the dataset files in a way that fully supports their understanding or reanalysis. Here we propose to develop the transcriptomics data format MAGE-TAB into a standard representation for proteomics sample metadata. We implement MAGE-TAB-Proteomics in a crowdsourcing project to manually curate over 200 public datasets. We also describe tools and libraries to validate and submit sample metadata-related information to the PRIDE repository. We expect that these developments will improve the reproducibility and facilitate the reanalysis and integration of public proteomics datasets. Y1 - 2021 U6 - https://doi.org/https://doi.org/10.1038/s41467-021-26111-3 VL - 12 IS - 5854 ER - TY - JOUR A1 - Bai, Mingze A1 - Deng, Jingwen A1 - Dai, Chengxin A1 - Pfeuffer, Julianus A1 - Sachsenberg, Timo A1 - Perez-Riverol, Yasset T1 - LFQ-Based Peptide and Protein Intensity Differential Expression Analysis JF - J. Proteome Res. N2 - Testing for significant differences in quantities at the protein level is a common goal of many LFQ-based mass spectrometry proteomics experiments. Starting from a table of protein and/or peptide quantities from a given proteomics quantification software, many tools and R packages exist to perform the final tasks of imputation, summarization, normalization, and statistical testing. To evaluate the effects of packages and settings in their substeps on the final list of significant proteins, we studied several packages on three public data sets with known expected protein fold changes. We found that the results between packages and even across different parameters of the same package can vary significantly. In addition to usability aspects and feature/compatibility lists of different packages, this paper highlights sensitivity and specificity trade-offs that come with specific packages and settings. Y1 - 2023 U6 - https://doi.org/10.1021/acs.jproteome.2c00812 VL - 22 IS - 6 SP - 2114 EP - 2123 PB - American Chemical Society ER -