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SJARACNe: a scalable software tool for gene network reverse engineering from big data
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....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581437/ https://www.ncbi.nlm.nih.gov/pubmed/30388204 http://dx.doi.org/10.1093/bioinformatics/bty907 |
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author | Khatamian, Alireza Paull, Evan O Califano, Andrea Yu, Jiyang |
author_facet | Khatamian, Alireza Paull, Evan O Califano, Andrea Yu, Jiyang |
author_sort | Khatamian, Alireza |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6581437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-65814372019-06-21 SJARACNe: a scalable software tool for gene network reverse engineering from big data Khatamian, Alireza Paull, Evan O Califano, Andrea Yu, Jiyang Bioinformatics Applications Notes 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. Oxford University Press 2019-06 2018-11-02 /pmc/articles/PMC6581437/ /pubmed/30388204 http://dx.doi.org/10.1093/bioinformatics/bty907 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Applications Notes Khatamian, Alireza Paull, Evan O Califano, Andrea Yu, Jiyang SJARACNe: a scalable software tool for gene network reverse engineering from big data |
title | SJARACNe: a scalable software tool for gene network reverse engineering from big data |
title_full | SJARACNe: a scalable software tool for gene network reverse engineering from big data |
title_fullStr | SJARACNe: a scalable software tool for gene network reverse engineering from big data |
title_full_unstemmed | SJARACNe: a scalable software tool for gene network reverse engineering from big data |
title_short | SJARACNe: a scalable software tool for gene network reverse engineering from big data |
title_sort | sjaracne: a scalable software tool for gene network reverse engineering from big data |
topic | Applications Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581437/ https://www.ncbi.nlm.nih.gov/pubmed/30388204 http://dx.doi.org/10.1093/bioinformatics/bty907 |
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