Related Experiment Video
Updated: Oct 9, 2025

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
Published on: June 21, 2018
ROHMM-A flexible hidden Markov model framework to detect runs of homozygosity from genotyping data
1Health Sciences Institute, Department of Medical Genetics, Ankara Yildirim Beyazit University, Ankara, Turkey.
Abstract:
Runs of long homozygous (ROH) stretches are considered to be the result of consanguinity and usually contain recessive deleterious disease-causing mutations. Several algorithms have been developed to detect ROHs. Here, we developed a simple alternative strategy by examining X chromosome non-pseudoautosomal region to detect the ROHs from next-generation sequencing data utilizing the genotype probabilities and the hidden Markov model algorithm as a tool, namely ROHMM. It is implemented purely in java and contains both a command line and a graphical user interface. We tested ROHMM on simulated data as well as real population data from the 1000G Project and a clinical sample. Our results have shown that ROHMM can perform robustly producing highly accurate homozygosity estimations under all conditions thereby meeting and even exceeding the performance of its natural competitors.
Related Concept Videos
Point and Frameshift Mutations
Mutation, Gene Flow, and Genetic Drift
Single Nucleotide Polymorphisms-SNPs
Genetic Variation
Genes exist in different versions called alleles,...
Genetic Drift
Multiple Allele Traits

