CHIT

CHIT combines allele-specific and total read counts from next-generation sequencing to test for genotype–phenotype interactions and increase power in association studies of molecular quantitative traits such as gene expression.


Key Features:

  • Allele-Specific Analysis: Leverages allele-specific read counts from next-generation sequencing to capture subtle variations in molecular traits that may be missed by conventional analyses.
  • Phenotype-Genotype Interaction Testing: Tests for interactions between phenotypic factors and genotypes that influence the expression of quantitative traits.
  • Modeling Approach: Models both total read counts and allele-specific reads within a target genomic region rather than relying solely on standard linear regression methods.
  • Supplementary Analysis Capability: Functions as an adjunct to conventional linear interaction regression analyses to provide additional insight into genetic architecture.

Scientific Applications:

  • Genotype–Environment and Phenotype Interactions: Applied to studies assessing how genetic variants interact with environmental or phenotypic factors to affect molecular quantitative traits.
  • Childhood Asthma (Puerto Ricans): Used to assess gene expression interactions with single nucleotide polymorphisms (SNPs) and atopy status in childhood asthma among Puerto Ricans.

Methodology:

Statistical framework that models total and allele-specific read counts, maintains non-inflated type I error rates, and yields greater power compared with traditional interaction quantitative trait locus approaches.

Topics

Details

Tool Type:
command-line tool
Programming Languages:
Python, C, Perl
Added:
11/20/2021
Last Updated:
11/24/2024

Operations

Publications

Yan Q, Forno E, Celedón JC, Chen W, Weeks DE. CHIT: an allele-specific method for testing the association between molecular quantitative traits and phenotype–genotype interaction. Bioinformatics. 2021;37(24):4764-4770. doi:10.1093/bioinformatics/btab554. PMID:34323937. PMCID:PMC8711119.

PMID: 34323937
PMCID: PMC8711119
Funding: - National Institutes of Health: HL079966, HL117191, HL138098, HL150431, MD011764