Evidence map›Paper›PMID 21601083›Full record

ArticleMethods in enzymology2011

Using DNA microarrays to assay part function.

Virgil A Rhodius, Carol A Gross

Abstract read
In one paragraph

Article in Methods in enzymology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Transcriptomic data sets examining several stress responses inMicrobiology resource announcements · 2026
    Article
  2. Review
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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.

Virgil A RhodiusDepartment of Microbiology and Immunology, University of California at San Francisco, San Francisco, California, USA.
Carol A Gross

Funding

MUTATIONAL ANALYSIS OF E COLI CORE RNA POLYMERASER01GM057755 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GROSS, CAROL ANNE · 1998 to 2013
$6.2M
NIGMS NIH HHS R01 GM057755
6 · The paper itself

Abstract

In recent years, the capability of synthetic biology to design large genetic circuits has dramatically increased due to rapid advances in DNA synthesis technology and development of tools for large-scale assembly of DNA fragments. Large genetic circuits require more components (parts), especially regulators such as transcription factors, sigma factors, and viral RNA polymerases to provide increased regulatory capability, and also devices such as sensors, receivers, and signaling molecules. All these parts may have a potential impact upon the host that needs to be considered when designing and fabricating circuits. DNA microarrays are a well-established technique for global monitoring of gene expression and therefore are an ideal tool for systematically assessing the impact of expressing parts of genetic circuits in host cells. Knowledge of part impact on the host enables the user to design circuits from libraries of parts taking into account their potential impact and also to possibly modify the host to better tolerate stresses induced by the engineered circuit. In this chapter, we present the complete methodology of performing microarrays from choice of array platform, experimental design, preparing samples for array hybridization, and associated data analysis including preprocessing, normalization, clustering, identifying significantly differentially expressed genes, and interpreting the data based on known biology. With these methodologies, we also include lists of bioinformatic resources and tools for performing data analysis. The aim of this chapter is to provide the reader with the information necessary to be able to systematically catalog the impact of genetic parts on the host and also to optimize the operation of fully engineered genetic circuits.

Indexed as

AlgorithmsCarbocyaninesFluorescent DyesGene Expression ProfilingOligonucleotide Array Sequence AnalysisResearch DesignRNASoftwareSynthetic BiologyCarbocyaninescyanine dye 3cyanine dye 5Fluorescent DyesRNA

Identifiers

PMID21601083
PMCPMC5433866

What OpenQuestion holds

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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.