Evidence map›Paper›PMID 38902827›Full record

ReviewFrontiers in zoology2024

De novo assembly of transcriptomes and differential gene expression analysis using short-read data from emerging model organisms - a brief guide.

Daniel J Jackson, Nicolas Cerveau, Nico Posnien

Abstract readReview
In one paragraph

Review in Frontiers in zoology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Frontiers in microbiology · 2025
    Article
  11. 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.

Daniel J Jackson *University of Göttingen, Department of Geobiology, Goldschmidtstr.3, Göttingen, 37077, Germany. djackso@gwdg.de.ORCID http://orcid.org/0000-0001-9045-381X
Nicolas Cerveau *University of Göttingen, Department of Geobiology, Goldschmidtstr.3, Göttingen, 37077, Germany.ORCID http://orcid.org/0000-0003-1962-3227
Nico Posnien *University of Göttingen, Department of Developmental Biology, GZMB, Justus-Von-Liebig-Weg 11, Göttingen, 37077, Germany. nposnie@gwdg.de.ORCID http://orcid.org/0000-0003-0700-5595

Funding

Deutsche Forschungsgemeinschaft 528314512Deutsche Forschungsgemeinschaft PO 1648/6-1Deutsche Forschungsgemeinschaft PO 1648/7-1Deutsche Forschungsgemeinschaft PO 1648/8-1
6 · The paper itself

Abstract

Many questions in biology benefit greatly from the use of a variety of model systems. High-throughput sequencing methods have been a triumph in the democratization of diverse model systems. They allow for the economical sequencing of an entire genome or transcriptome of interest, and with technical variations can even provide insight into genome organization and the expression and regulation of genes. The analysis and biological interpretation of such large datasets can present significant challenges that depend on the 'scientific status' of the model system. While high-quality genome and transcriptome references are readily available for well-established model systems, the establishment of such references for an emerging model system often requires extensive resources such as finances, expertise and computation capabilities. The de novo assembly of a transcriptome represents an excellent entry point for genetic and molecular studies in emerging model systems as it can efficiently assess gene content while also serving as a reference for differential gene expression studies. However, the process of de novo transcriptome assembly is non-trivial, and as a rule must be empirically optimized for every dataset. For the researcher working with an emerging model system, and with little to no experience with assembling and quantifying short-read data from the Illumina platform, these processes can be daunting. In this guide we outline the major challenges faced when establishing a reference transcriptome de novo and we provide advice on how to approach such an endeavor. We describe the major experimental and bioinformatic steps, provide some broad recommendations and cautions for the newcomer to de novo transcriptome assembly and differential gene expression analyses. Moreover, we provide an initial selection of tools that can assist in the journey from raw short-read data to assembled transcriptome and lists of differentially expressed genes.

Indexed as

AnnotationDe novo assemblyDifferential gene expressionEmerging model systemGenomeRNA-seqShort readsTranscriptome assembly

Identifiers

PMID38902827
PMCPMC11188175

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.