A new method for detecting human recombination hotspots and its applications to the HapMap ENCODE data.

Abstract

Computational detection of recombination hotspots from population polymorphism data is important both for understanding the nature of recombination and for applications such as association studies. We propose a new method for this task based on a multiple-hotspot model and an (approximate) log-likelihood ratio test. A truncated, weighted pairwise log-likelihood is introduced and applied to the calculation of the log-likelihood ratio, and a forward-selection procedure is adopted to search for the optimal hotspot predictions. The method shows a relatively high power with a low false-positive rate in detecting multiple hotspots in simulation data and has a performance comparable to the best results of leading computational methods in experimental data for which recombination hotspots have been characterized by sperm-typing experiments. The method can be applied to both phased and unphased data directly, with a very fast computational speed. We applied the method to the 10 500-kb regions of the HapMap ENCODE data and found 172 hotspots among the three populations, with average hotspot width of 2.4 kb. By comparisons with the simulation data, we found some evidence that hotspots are not all identical across populations. The correlations between detected hotspots and several genomic characteristics were examined. In particular, we observed that DNaseI-hypersensitive sites are enriched in hotspots, suggesting the existence of human beta hotspots similar to those found in yeast.