COVID-19 is an emerging, rapidly evolving siituation.

What people with cancer should know: https://www.cancer.gov/coronavirus

Guidance for cancer researchers: https://www.cancer.gov/coronavirus-researchers

Get the latest public health information from CDC: https://www.coronavirus.gov

Get the latest research information from NIH: https://www.nih.gov/coronavirus

FragPipe-Analyst: Advancing Quantitative Proteomics Analysis

Monday, December 16, 2024

CPTAC researchers from the University of Michigan and researchers from Monash University, Australia have developed a new software tool to complement the widely used FragPipe computational proteomics platform. FragPipe-Analyst (FP-A) is designed to streamline downstream statistical analysis and data visualization, simplifying the exploration of dense proteomics datasets.

FragPipe is an open-source software pipeline for mass spectrometry-based proteomics, offering tools like MSFragger for peptide identification, IonQuant for label-free quantification, and PTM-Shepherd for modification analysis. While FragPipe provides a robust platform for upstream data processing, downstream statistical and visualization steps remain critical for deriving insights in proteomics.

FP-A is a web-based application with a user-friendly interface that allows users to directly upload FragPipe-generated files from a variety of quantification workflows (DDA, DIA, TMT, etc.) for downstream analysis and visualization. Like FragPipe, FP-A is completely open-source and freely available, with extensive documentation and tutorials for new users.

FP-A includes a range of downstream data processing features such as missing value filtering, data normalization, and missing value imputation. Once the data is processed, FP-A can automatically identify significant changes and patterns through differential expression analysis and sample clustering. After data processing and analysis, FP-A readily visualizes data (PCA plots, volcano plots, heatmaps) to facilitate quality assessment, enhance data interpretation, and aid in the sharing of results.

Yi Hsiao, a Ph.D. candidate from University of Michigan who led the project commented on FP-A’s value and ease of use, saying “the tools are used by graduate students who are beginners in proteomics and don’t have much programming experience. As a bioinformatics student, it’s always thrilling to have tools be useful for many users.”

FP-A’s companion program, FragPipeAnalystR (FPAR), is an R package that maintains the same functionality while allowing for further modification of analysis workflows and integration with other R packages. So far, FP-A/FPAR has demonstrated its capabilities through reanalysis of existing proteomics studies, including CPTAC research on clear cell renal cell carcinoma. As FP-A/FPAR continues to be developed, the team plans to expand support for additional PTMs and improve integration with multiomics workflows.

To access these tools, use the links below.

Tool Link
FragPipe https://fragpipe.nesvilab.org/
FragPipe-Analyst https://fragpipe-analyst-doc.nesvilab.org/
FragPipeAnalystR https://www.nesvilab.org/FragPipeAnalystR/