Abstract Summary Over the last two decades, we have observed an exponential increase in the number of generated array or sequencing-based transcriptomic profiles. Reverse engineering of biological networks from high-throughput gene expression profiles has been one of the grand challenges in systems biology. The Algorithm for the Reconstruction of Accurate Cellular Networks (ARACNe) represents one of the most effective and widely-used tools to address this challenge. However, existing ARACNe implementations do not efficiently process big input data with thousands of samples. Here we present an improved implementation of the algorithm, SJARACNe, to solve this big data problem, based on sophisticated software engineering. The new scalable SJARACNe package achieves a dramatic improvement in computational performance in both time and memory usage and implements new features while preserving the network inference accuracy of the original algorithm. Given that large-sampled transcriptomic data is increasingly available and ARACNe is extremely demanding for network reconstruction, the scalable SJARACNe will allow even researchers with modest computational resources to efficiently construct complex regulatory and signaling networks from thousands of gene expression profiles. Availability and implementation SJARACNe is implemented in C++ (computational core) and Python (pipelining scripting wrapper, ≥3.6.1). It is freely available at https://github.com/jyyulab/SJARACNe. Supplementary information Supplementary data are available at Bioinformatics online.
[1]
Haiyan Tan,et al.
Hippo/Mst signalling couples metabolic state and immune function of CD8α+ dendritic cells
,
2018,
Nature.
[2]
Andrea Califano,et al.
Direct reversal of glucocorticoid resistance by AKT inhibition in acute lymphoblastic leukemia.
,
2013,
Cancer cell.
[3]
Chris Wiggins,et al.
ARACNE: An Algorithm for the Reconstruction of Gene Regulatory Networks in a Mammalian Cellular Context
,
2004,
BMC Bioinformatics.
[4]
Andrea Califano,et al.
ARACNe-AP: gene network reverse engineering through adaptive partitioning inference of mutual information
,
2016,
Bioinform..
[5]
A. Califano,et al.
Inhibition of the autocrine IL-6-JAK2-STAT3-calprotectin axis as targeted therapy for HR-/HER2+ breast cancers.
,
2015,
Genes & development.
[6]
F. Markowetz,et al.
The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups
,
2012,
Nature.
[7]
María Rodríguez Martínez,et al.
Elucidating Compound Mechanism of Action by Network Perturbation Analysis Graphical
,
2015
.