bioRxivBioinformaticsPreprint
TaoChongBao: A Large-Scale Caenorhabditis elegans Mutagenesis and Missense Variant Database Bridging Worm and Human Genomes
Ming LiiD, Shimin WangiD, Yongping ChaiiD, Zhengyang GuoiD, Zi WangiD, Zhe CheniD, Kexin LeiiD, Jingyi KeiD, Xingshen Huang, Kaiming XuiD, Zijie SheniD, Wei LiiD, Guangshuo OuiD
- Citations
- 0
Abstract
We generated and sequenced 12,069 viable Caenorhabditis elegans strains produced by ethyl methanesulfonate mutagenesis, identifying 20,315,536 variants, including 541,102 unique missense mutations across 20,914 genes. To organize and visualize this resource, we developed TaoChongBao, an open-access database and strain repository that integrates C. elegans mutation data with AlphaMissense-predicted pathogenicity scores and ClinVar clinical annotations. TaoChongBao enables users to explore worm missense variants, identify conserved residues corresponding to human pathogenic sites, and access viable strains for experimental validation. Compared with the previous Million Mutation Project in C. elegans, TaoChongBao expands mutation coverage over twenty-fold and emphasizes amino acid-altering variants. This resource provides a scalable platform for functional residuomics, variant interpretation, and comparative analyses between C. elegans and human genomes.
- organism: C. elegans
- assay: DNA methylation
- assay: whole-genome sequencing
- research focus: database / resource
- research focus: variant effect prediction
- research focus: GWAS / association mapping
- research focus: eQTL / molecular QTL mapping
- approach: statistical model
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- CRISPR-Cas9 human gene replacement and phenomic characterization in Caenorhabditis elegans to understand the functional conservation of human genes and decipher variants of uncertain significance
Troy A. McDiarmid, Vinci Au, … Catharine H. Rankin·Disease Models & MechanismsPeer-reviewed·Jan 1, 2018
- Natural variation in C. elegans short tandem repeats
Gaotian Zhang, Ye Wang, Erik C. Andersen·Genome ResearchPeer-reviewed·Oct 4, 2022
- ConVarT: a search engine for matching human genetic variants with variants from non-human species
Mustafa S Pir, Halil Bilgin, … Oktay I. Kaplan·Nucleic Acids ResearchPeer-reviewed·Oct 15, 2021
- High-throughput behavioural phenotyping of 25 C. elegans disease models including patient-specific mutations
Thomas James O’Brien, Emma Lara Navarro, … André EX Brown·BMC BiologyPeer-reviewed·Sep 26, 2025
- Matching Variants for functional characterization of genetic variants
Sebiha Cevik, Pei Zhao, … Oktay I. Kaplan·G3 Genes Genomes GeneticsPeer-reviewed·Oct 27, 2023
- Genome structural variation in natural Caenorhabditis elegans populations
Kyle J. Lesack, James D. Wasmuth·bioRxiv·Jan 7, 2025