Enhancement of hidden Markov model analyses for improved inference of archaic introgression in modern humans
Coll Macia, M.; Skov, L.; Baek, Z. E. D.; Hobolth, A.
Show abstract
Insights into the admixture history between modern and archaic humans require accurately inferred introgressed fragments within modern genomes. Here, we introduce two enhancements to hidden Markov models (HMMs) implemented in hmmix. First, we develop a method for sampling hidden state sequences conditional on observed genomic data, enabling robust estimation of admixture summary statistics--such as admixture proportion and fragment length distributions. This represents an improvement compared to relying solely on point estimates as provided by classical decoding methods. Additionally, we integrate the Finite Markov Chain Imbedding (FMCI) framework, allowing exact analytical calculation of these admixture statistics, tailored to large scale human genomes. Second, we implement a novel hybrid decoding method which combines the strengths of Viterbi and Posterior decoding methods, substantially improving the reliability of archaic fragments identified. We validate these improvements on data from the 1000 Genomes Project and demonstrate that our sampling method yield more accurate admixture estimates from single individuals compared to existing approaches requiring extensive population-level datasets. Moreover we show how hybrid decoding can be instrumental in resolving the inference of local archaic haplotype structure in modern human genomes. These methodological advancements broadly enhance HMM-based analyses and will provide deeper insight into the complex history of genetic interactions between archaic and modern human populations.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Generative Haplotype Prediction Outperforms Statistical Methods for Small Variant Detection in NGS Data 96%
- hapCon: Estimating contamination of ancient genomes by copying from reference haplotypes 96%
- Efficient toolkit implementing best practices for principal component analysis of population genetic data 96%
Similar papers in this journal
"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.