Evidence map›Paper›PMID 38909042›Full record

ArticleScientific data2024

Chromosome-level genome assembly and annotation of the social amoeba Dictyostelium firmibasis.

Bart Edelbroek, Jonas Kjellin, Jon Jerlström-Hultqvist, Sanna Koskiniemi, Fredrik Söderbom

Abstract readDataset
In one paragraph

Article in Scientific data, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Hypermutable hotspot enables the rapid evolution of self/non-self recognition genes inProceedings of the National Academy of Sciences of the United States of America · 2025
    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

5 authors.

Bart EdelbroekDepartment of Cell and Molecular Biology, BMC, Uppsala University, SE-751 24, Uppsala, Sweden. bart.edelbroek@gmail.com.ORCID 0000-0002-5184-0873
Jonas KjellinDepartment of Cell and Molecular Biology, BMC, Uppsala University, SE-751 24, Uppsala, Sweden.ORCID 0000-0002-3830-7046
Jon Jerlström-HultqvistDepartment of Cell and Molecular Biology, BMC, Uppsala University, SE-751 24, Uppsala, Sweden.
Sanna KoskiniemiDepartment of Cell and Molecular Biology, BMC, Uppsala University, SE-751 24, Uppsala, Sweden.
Fredrik SöderbomDepartment of Cell and Molecular Biology, BMC, Uppsala University, SE-751 24, Uppsala, Sweden. fredrik.soderbom@icm.uu.se.ORCID 0000-0003-3616-3509

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dicytostelium firmibasis is a member of Dictyostelia, a group of social amoebae that upon starvation display aggregative multicellularity where the amoebae transition from uni- to multicellular life. The D. firmibasis genome assembly that is currently available is of limited use due to its low contiguity, large number of undetermined bases, and lack of annotations. Here we used Nanopore long read sequencing, complemented with Illumina sequencing, and developmental transcriptomics as well as small RNA-sequencing, to present a new, fully annotated, chromosome-level D. firmibasis genome assembly. The new assembly contains no undetermined bases, and consists mainly of six large contigs representing the chromosomes, as well as a complete mitochondrial genome. This new genome assembly will be a valuable tool, allowing comprehensive comparison to Dictyostelium discoideum, the dictyostelid genetically tractable model. Further, the new genome will be important for studies of evolutionary processes governing the transition from unicellular to multicellular organisms and will aid in the sequencing and annotation of other dictyostelids genomes, many of which are currently of poor quality.

Indexed as

ChromosomesDictyosteliumGenome, ProtozoanMolecular Sequence Annotation

Identifiers

PMID38909042
PMCPMC11193728

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Registered trials

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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.