Evidence map›Paper›PMID 35348662›Full record

ArticleGenome biology and evolution2022

Chromosome-Level Reference Genomes for Two Strains of Caenorhabditis briggsae: An Improved Platform for Comparative Genomics.

Lewis Stevens, Nicolas D Moya, Robyn E Tanny, Sophia B Gibson, Alan Tracey, Huimin Na, Rojin Chitrakar, Job Dekker, Albertha J M Walhout, L Ryan Baugh and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
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

39 citing papers in PubMed, 41 citations in OpenAlex.

  1. T2T genomes ofGenome research · 2026
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  9. A gap-free, telomere-to-telomere genome assembly for thebioRxiv : the preprint server for biology · 2026
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  10. Global genomic diversity of the selfing nematodebioRxiv : the preprint server for biology · 2026
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  11. Natural variation suggests candidate genes underlying Caenorhabditis elegans susceptibility to diverse toxicants.Toxicological sciences : an official journal of the Society of Toxicology · 2026
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  14. High-Throughput Toxicity Screening withEnvironmental science & technology · 2026
    Review
  15. bioRxiv : the preprint server for biology · 2025
    Article
  16. Natural variation suggests candidate genes underlyingbioRxiv : the preprint server for biology · 2025
    Article
  17. Article
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  20. 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

11 authors at 4 institutions in 2 countries.

Lewis StevensDepartment of Molecular Biosciences, Northwestern University, Evanston, Illinois, USA.ORCID 0000-0002-6075-8273
Nicolas D MoyaDepartment of Molecular Biosciences, Northwestern University, Evanston, Illinois, USA.
Robyn E TannyDepartment of Molecular Biosciences, Northwestern University, Evanston, Illinois, USA.
Sophia B GibsonDepartment of Molecular Biosciences, Northwestern University, Evanston, Illinois, USA.ORCID 0000-0001-9839-9045
Alan TraceyTree of Life, Wellcome Sanger Institute, Cambridge, UK.
Huimin NaDepartment of Systems Biology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Rojin ChitrakarDepartment of Biology, Duke University, Durham, North Carolina, USA.
Job DekkerDepartment of Systems Biology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Albertha J M WalhoutDepartment of Systems Biology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
L Ryan BaughDepartment of Biology, Duke University, Durham, North Carolina, USA.
Erik C AndersenDepartment of Molecular Biosciences, Northwestern University, Evanston, Illinois, USA.ORCID 0000-0003-0229-9651
Northwestern University · USUniversity of Massachusetts Chan Medical School · USDuke University · USWellcome Sanger Institute · GB

Funding

Gene regulatory and metabolic network structure, function and evolutionR35GM122502 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI A. J. Marian Walhout · 2017 to 2026
$8.3M
Developing Capacity to Evaluate Training Programs via Development of Human, Institutional and Social CapitalT32GM008449 · NIGMS · NORTHWESTERN UNIVERSITY · PI LEONARD, JOSHUA NATHANIEL · 1993 to 2023
$7.8M
Discovery of conserved molecular mechanisms underlying population-wide variation in toxin responsesR01ES029930 · NIEHS · NORTHWESTERN UNIVERSITY · PI ANDERSEN, ERIK CHRISTIAN, BAUGH, LARRY RYAN · 2019 to 2023
$3.2M
Howard Hughes Medical InstituteNIEHS NIH HHS R01 ES029930NIGMS NIH HHS R35 GM122502NIGMS NIH HHS T32 GM008449
6 · The paper itself

Abstract

The publication of the Caenorhabditis briggsae reference genome in 2003 enabled the first comparative genomics studies between C. elegans and C. briggsae, shedding light on the evolution of genome content and structure in the Caenorhabditis genus. However, despite being widely used, the currently available C. briggsae reference genome is substantially less complete and structurally accurate than the C. elegans reference genome. Here, we used high-coverage Oxford Nanopore long-read and chromosome-conformation capture data to generate chromosome-level reference genomes for two C. briggsae strains: QX1410, a new reference strain closely related to the laboratory AF16 strain, and VX34, a highly divergent strain isolated in China. We also sequenced 99 recombinant inbred lines generated from reciprocal crosses between QX1410 and VX34 to create a recombination map and identify chromosomal domains. Additionally, we used both short- and long-read RNA sequencing data to generate high-quality gene annotations. By comparing these new reference genomes to the current reference, we reveal that hyper-divergent haplotypes cover large portions of the C. briggsae genome, similar to recent reports in C. elegans and C. tropicalis. We also show that the genomes of selfing Caenorhabditis species have undergone more rearrangement than their outcrossing relatives, which has biased previous estimates of rearrangement rate in Caenorhabditis. These new genomes provide a substantially improved platform for comparative genomics in Caenorhabditis and narrow the gap between the quality of genomic resources available for C. elegans and C. briggsae.

Indexed as

CaenorhabditisAnimalsCaenorhabditis elegansChromosomesGenomeGenomicsCaenorhabditis briggsaecomparative genomicsgenetic diversitygenome rearrangementreference genomesselfing

Identifiers

PMID35348662
PMCPMC9011032
OpenAlexW4220736078

What OpenQuestion holds

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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.