Evidence map›Paper›PMID 20827605›Full record

ReviewMethods in molecular biology (Clifton, N.J.)2010

Computational methods for analyzing dynamic regulatory networks.

Anthony Gitter, Yong Lu, Ziv Bar-Joseph

Abstract readReview
In one paragraph

Review in Methods in molecular biology (Clifton, N.J.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

3 authors.

Anthony GitterComputer Science Department, Carnegie Mellon University, Pittsburgh, PA, USA. agitter@cs.cmu.edu
Yong Lu
Ziv Bar-Joseph

Funding

Reconstructing dynamic regulatory networksR01GM085022 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI BAR-JOSEPH, ZIV · 2008 to 2011
$1.1M
NIGMS NIH HHS R01 GM085022
6 · The paper itself

Abstract

Regulatory and other networks in the cell change in a highly dynamic way over time and in response to internal and external stimuli. While several different types of high-throughput experimental procedures are available to study systems in the cell, most only measure static properties of such networks. Information derived from sequence data is inherently static, and most interaction data sets are measured in a static way as well. In this chapter we discuss one of the few abundant sources for temporal information, time series expression data. We provide an overview of the methods suggested for clustering this type of data to identify functionally related genes. We also discuss methods for inferring causality and interactions using lagged correlations and regression analysis. Finally, we present methods for combining time series expression data with static data to reconstruct dynamic regulatory networks. We point to software tools implementing the methods discussed in this chapter. As more temporal measurements become available, the importance of analyzing such data and of combining it with other types of data will greatly increase.

Indexed as

Gene Regulatory NetworksAnimalsCluster AnalysisComputational BiologyHumansSoftwareTime Factors

Identifiers

PMID20827605
PMCPMC8704440

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.