Journal
JOURNAL OF PROTEOME RESEARCH
Volume 20, Issue 4, Pages 2116-2121Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.0c00963
Keywords
proteomics; phosphoproteomics; pathway analysis; data integration
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Funding
- National Cancer Institute Clinical Proteomic Tumor Analysis Consortium (CPTAC) [U01CA214116, U24CA210955]
- Laboratory Directed Research and Development Program at Pacific Northwest National Laboratory [DE-AC05-76RL01830]
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The goal of high-throughput data studies is to identify functional mechanisms underlying biological phenomena, which requires time-consuming evaluation of various statistical methods. The leapR package allows rapid assessment of biological pathway activity, facilitating integration of multisource data.
A generalized goal of many high-throughput data studies is to identify functional mechanisms that underlie observed biological phenomena, whether they be disease outcomes or metabolic output. Increasingly, studies that rely on multiple sources of high-throughput data (genomic, transcriptomic, proteomic, metabolomic) are faced with a challenge of summarizing the data to generate testable hypotheses. However, this requires a time-consuming process to evaluate numerous statistical methods across numerous data sources. Here, we introduce the leapR package, a framework to rapidly assess biological pathway activity using diverse statistical tests and data sources, allowing facile integration of multisource data. The leapR package with a user manual and example workflow is available for download from GitHub (fittps:/,/githithcornibiodataganache/leapR).
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