Evidence map›Paper›PMID 42312323›Full record

ArticleG3 (Bethesda, Md.)2026

A gap-free, telomere-to-telomere genome assembly for the Caenorhabditis briggsae reference strain AF16.

Lance M O'Connor, Nicolas D Moya, Nikita S Jhaveri, Robyn E Tanny, Ayeh Khorshidian, Haimeng Lyu, Helen M Chamberlin, Scott E Baird, Erik C Andersen

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. T2T genomes ofGenome research · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Lance M O'ConnorDepartment of Biology, Johns Hopkins University, Bascom UTL 383, Baltimore, MD 21218, United States.ORCID 0009-0007-1373-183X
Nicolas D MoyaDepartment of Biology, Johns Hopkins University, Bascom UTL 383, Baltimore, MD 21218, United States.ORCID 0000-0002-6817-1784
Nikita S JhaveriDepartment of Biology, Johns Hopkins University, Bascom UTL 383, Baltimore, MD 21218, United States.ORCID 0009-0008-6434-2188
Robyn E TannyDepartment of Biology, Johns Hopkins University, Bascom UTL 383, Baltimore, MD 21218, United States.ORCID 0000-0002-0611-3909
Ayeh KhorshidianDepartment of Biology, Johns Hopkins University, Bascom UTL 383, Baltimore, MD 21218, United States.ORCID 0009-0002-6855-9137
Haimeng LyuDepartment of Molecular Genetics, The Ohio State University, Columbus, OH 43210, United States.
Helen M ChamberlinDepartment of Molecular Genetics, The Ohio State University, Columbus, OH 43210, United States.ORCID 0000-0001-7203-2691
Scott E BairdDepartment of Biological Sciences, Wright State University, Dayton, OH 43435, United States.ORCID 0000-0002-8084-9383
Erik C AndersenDepartment of Biology, Johns Hopkins University, Bascom UTL 383, Baltimore, MD 21218, United States.ORCID 0000-0003-0229-9651

Funding

WormBase: a core data resource for C. elegans and other nematodesU24HG002223 · NHGRI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI TIM SCHEDL, PAUL Warren STERNBERG · 2018 to 2026
$18.9M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Genetic and genomic tools for C. briggsae researchR21OD030067 · OD · OHIO STATE UNIVERSITY · PI ANDERSEN, ERIK CHRISTIAN, CHAMBERLIN, HELEN M · 2022 to 2023
$431k
NHGRI NIH HHS U24 HG002223NIH HHS P40 OD010440NIH HHS R21 OD030067NIH R21 Exploratory/Developmental R21OD030067
6 · The paper itself

Abstract

The nematode Caenorhabditis elegans was the first metazoan to have its genome completely sequenced and assembled. Since that time, researchers have continuously updated the reference genome and manually curated its approximately 20,000 genes. The closely related species, Caenorhabditis briggsae, has served as a comparative model because of its similar morphology, mode of reproduction, and patterns of intraspecies genetic variation. However, the genomic resources for C. briggsae lag behind C. elegans, hindering comparative genomics studies between the species. Decades of experimentation have been performed in the AF16 reference strain genetic background, so we obtained high-coverage long-read sequencing and high-throughput chromosome conformation capture data to create an updated reference genome for an isogenic derivative of AF16, named CGC2. The CGC2 genome is vastly improved relative to the existing AF16 assemblies, with no unplaced sequence, no gaps, and telomere-to-telomere contiguity. To provide genomic resources for CGC2, we exploited deep RNA-seq libraries from all developmental stages to predict protein-coding gene annotations comparable in accuracy and completeness to the existing AF16 gene models. We also performed a liftover of 108 validated insertion-deletion variants to the updated coordinate system of the CGC2 genome to facilitate future mappings of mutations. In summary, we present an updated reference genome for the canonical AF16 reference strain with improved genomic resources to enable high-quality intra- and interspecies comparative studies.

Indexed as

CaenorhabditisGenome, HelminthGenomicsTelomereAnimalsMolecular Sequence AnnotationAF16Caenorhabditis briggsaeCGC2genomegenome annotationgenome assembly

Identifiers

PMID42312323
PMCPMC13439942

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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.