ALPACA

Detecting phenotype-driven transitions in regulatory network structure (also on the bioRxiv)

Complex traits and diseases like human height or cancer are often not caused by a single mutation or genetic variant, but instead arise from multiple factors that together functionally perturb the underlying molecular network. Biological networks are known to be highly modular and contain dense “communities” of genes that carry out cellular processes, but these structures change between tissues, during development, and in disease. While many methods exist for inferring networks, we lack robust methods for quantifying changes in network structure. Here, we describe ALPACA (ALtered Partitions Across Community Architectures), a method for comparing two genome-scale networks derived from different phenotypic states to identify condition-specific modules. In simulations, ALPACA leads to more nuanced, sensitive, and robust module discovery than currently available network comparison methods. We used ALPACA to compare transcriptional networks in three contexts: angiogenic and non-angiogenic subtypes of ovarian cancer, human fibroblasts expressing transforming viral oncogenes, and sexual dimorphism in human breast tissue. In each case, ALPACA identified modules enriched for processes relevant to the phenotype. For example, modules specific to angiogenic ovarian tumors were enriched for genes associated with blood vessel development, interferon signaling, and flavonoid biosynthesis. In comparing the modular structure of networks in female and male breast tissue, we found that female breast has distinct modules enriched for genes involved in estrogen receptor and ERK signaling. The functional relevance of these new modules indicate that not only does phenotypic change correlate with network structural changes, but also that ALPACA can identify such modules in complex networks.

Papers citing ALPACA