COBT: A gene-based rare variant burden test for case-only study designs using aggregated genotypes from public reference cohorts.
Favier, A.; Chounta, S.; Garcia, A.; Jabot-Hanin, F.; Chen, X.; Garcelon, N.; Burgun, A.; Higueras, M.; Guilloux, A.; Benmerah, A.; Martin, Y.; Billot, K.; Rozet, J.-M.; Perrault, I.; Cormier-Daire, V.; Huber, C.; Zaidan, M.; Attie-Bitach, T.; Saunier, S.; Rausell, A.
Show abstract
More than 4000 rare genetic diseases affect 1 in 16 people, yet [~]50% of patients remain undiagnosed after genetic testing. Identifying genotype-phenotype associations is challenged by small cohorts and high clinical and genetic heterogeneity. Rare variant burden tests increase statistical power in case-control studies, but are limited in rare disease research due to the lack of matched controls in retrospective studies. Recently proposed case-only aggregation tests assess the number of individuals with damaging variants under dominant or recessive models, but fail to capture additive effects, hypomorphic variants, or heterogeneous inheritance modes. Here, we present the Case-Only Burden Test (COBT), a gene-based burden test for case-only designs accounting for multiple variants per individual and their putative additive effects. COBT uses a Poisson model to test for excess variants in a gene compared to expectations from general population mutation rates. We validated the models assumptions and goodness-of-fit on a control cohort from the 1000 Genomes Project, where COBT showed low false-positive rates and outperformed alternative case-only tests. Applied to 478 ciliopathy patients, COBT re-identified known causal genes and highlighted novel candidate variants in unsolved cases. COBT enables gene discovery in case-only rare disease cohorts and is available at https://github.com/RausellLab/COBT.
Matching journals
The top 8 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Systematic analysis of genetic and phenotypic characteristics reveals antisense oligonucleotide therapy potential for one-third of neurodevelopmental disorders 95%
- Calculating variant penetrance using family history of disease and population data Authorship 94%
- Impact of rare and common genetic variation in theInterleukin-1 pathway for human cytokine responses 93%
Similar papers in this journal
- Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity 94%
- Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21 93%
- Common Genetic Risk Factors in ASD and ADHD Co-occurring Families 92%
Similar papers in this journal
Similar papers in this journal
- Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project 95%
- Polygenic risk score portability for common diseases across genetically diverse populations 93%
- Characterizing the polygenic architecture of complex traits in populations of East Asian and European descent 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.