--- license: cc-by-4.0 dataset_info: features: - name: Sequences dtype: string - name: Classes dtype: int64 splits: - name: train num_bytes: 6087276 num_examples: 236758 - name: val num_bytes: 1521645 num_examples: 59190 - name: test num_bytes: 845949 num_examples: 32884 download_size: 5786856 dataset_size: 8454870 configs: - config_name: default data_files: - split: train path: data/train-* - split: val path: data/val-* - split: test path: data/test-* --- # Detectability - ProteomeTools This data was collected from the PRIDE repository with the identifiers [PXD004732](https://www.ebi.ac.uk/pride/archive/projects/PXD004732), [PXD010595](https://www.ebi.ac.uk/pride/archive/projects/PXD010595), and [PXD021013](https://www.ebi.ac.uk/pride/archive/projects/PXD021013). The datasets were originally obtained by analyzing pools of approximately 1000 synthetic peptides. RAW data was analyzed using either specific, semi-specific, or unspecific in silico digestion settings in MaxQuant and with Trypsin, LysN, or AspN as specified protease. In all studies, peptide pools were subjected to liquid chromatography using a Dionex 3000 HPLC system (Thermo Fisher Scientific) coupled inline with an Orbitrap Fusion Lumos mass spectrometer (Thermo Fisher Scientific). ## Dataset Details - **Curated by:** Aalborg University - Denmark, in collaboration with Wilhelmlab - TU Munich. ### Dataset Sources The data is based on the ProteomeTools datasets introduced in [[1]](#ref1) and [[2]](#ref2) and available at: - https://www.ebi.ac.uk/pride/archive/projects/PXD004732 - https://www.ebi.ac.uk/pride/archive/projects/PXD010595 - https://www.ebi.ac.uk/pride/archive/projects/PXD021013 ## Uses The dataset is intended to be used for training, fine-tuning, and evaluating detectability prediction models, given a peptide sequence. Note that since the peptides were synthesized, training on the dataset will be somewhat biased to synthesizability, rathen than digestability. ## References [1] Zolg, D. P., Wilhelm, M., Schnatbaum, K., Zerweck, J., Knaute, T., Delanghe, B., ... & Kuster, B. (2017). Building ProteomeTools based on a complete synthetic human proteome. Nature methods, 14(3), 259-262.‏ [2] Gessulat, S., Schmidt, T., Zolg, D. P., Samaras, P., Schnatbaum, K., Zerweck, J., ... & Wilhelm, M. (2019). Prosit: proteome-wide prediction of peptide tandem mass spectra by deep learning. Nature methods, 16(6), 509-518.‏ ## Citation **BibTeX:** ```bibtex @article {Abdul-Khalek2024.10.28.620610, author = {Abdul-Khalek, Naim and Picciani, Mario and Wimmer, Reinhard and Overgaard, Michael Toft and Wilhelm, Mathias and Echers, Simon Gregersen}, title = {To fly, or not to fly, that is the question: A deep learning model for peptide detectability prediction in mass spectrometry}, elocation-id = {2024.10.28.620610}, year = {2024}, doi = {10.1101/2024.10.28.620610}, publisher = {Cold Spring Harbor Laboratory}, URL = {https://www.biorxiv.org/content/early/2024/10/31/2024.10.28.620610}, eprint = {https://www.biorxiv.org/content/early/2024/10/31/2024.10.28.620610.full.pdf}, journal = {bioRxiv} } ``` **APA:** Abdul-Khalek, N., Picciani, M., Wimmer, R., Overgaard, M. T., Wilhelm, M., & Gregersen Echers, S. (2024). To fly, or not to fly, that is the question: A deep learning model for peptide detectability prediction in mass spectrometry. bioRxiv, 2024-10.‏ ## Dataset Card Contact Simon Gregersen, sgr@bio.aau.dk, Department of Chemistry and Biosciences, Aalborg University. Mathias Wilhelm, mathias.wilhelm@tum.de, Wilhelmlab, TU Munich, School of Life Sciences, Germany.