Evidence map›Paper›PMID 30594121›Full record

ArticleBMC bioinformatics2018

Time-lagged Ordered Lasso for network inference.

Phan Nguyen, Rosemary Braun

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Inferring causal gene regulatory networkFrontiers in bioengineering and biotechnology · 2022
    Article
  8. Article
  9. Machine learning in postgenomic biology and personalized medicine.Wiley interdisciplinary reviews. Data mining and knowledge discovery
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Phan NguyenDepartment of Engineering Sciences and Applied Mathematics, Northwestern University, Evanston, IL, USA.
Rosemary BraunDepartment of Engineering Sciences and Applied Mathematics, Northwestern University, Evanston, IL, USA. rbraun@northwestern.edu.ORCID http://orcid.org/0000-0001-9668-9866

Funding

James S. McDonnell Foundation 220020394National Science Foundation DMS-1547394
6 · The paper itself

Abstract

backgroundAccurate gene regulatory networks can be used to explain the emergence of different phenotypes, disease mechanisms, and other biological functions. Many methods have been proposed to infer networks from gene expression data but have been hampered by problems such as low sample size, inaccurate constraints, and incomplete characterizations of regulatory dynamics. Since expression regulation is dynamic, time-course data can be used to infer causality, but these datasets tend to be short or sparsely sampled. In addition, temporal methods typically assume that the expression of a gene at a time point depends on the expression of other genes at only the immediately preceding time point, while other methods include additional time points without any constraints to account for their temporal distance. These limitations can contribute to inaccurate networks with many missing and anomalous links.

resultsWe adapted the time-lagged Ordered Lasso, a regularized regression method with temporal monotonicity constraints, for de novo reconstruction. We also developed a semi-supervised method that embeds prior network information into the Ordered Lasso to discover novel regulatory dependencies in existing pathways. R code is available at https://github.com/pn51/laggedOrderedLassoNetwork .

conclusionsWe evaluated these approaches on simulated data for a repressilator, time-course data from past DREAM challenges, and a HeLa cell cycle dataset to show that they can produce accurate networks subject to the dynamics and assumptions of the time-lagged Ordered Lasso regression.

Indexed as

Regression AnalysisGene ExpressionGene Regulatory NetworksHumansGene network reconstructionGene regulationLassoNetwork inferencePenalized regressionRegularizationTime course data

Identifiers

PMID30594121
PMCPMC6311035

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.