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Cumulative values of recombination over each interval was used because we were interested in comparing a recent population recombination map based on the observed pedigree with a historic population recombination map, rather than comparing point estimates of recombination rate per distance.
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Population specific recombination maps were independently estimated for each of the four populations using the LDhat program53, run with a block penalty of 5, 10 million rjMCMC iterations and a burn in of 100,000 iterations.
The YRI population is more strongly correlated with every recombination map than any other population.
To fully examine the relationship between recombination rates and efficacy of selection in Arabidopsis, higher resolution maps and/or population recombination rate estimates are needed.
This result holds across length scales and even when comparing YRI W→S DAF skew to a recombination map from another HapMap population or the Icelandic population.
This holds for both the recombination map specific to the population considered and the combined map based on all polymorphism data.
This finding suggests that we are converging on the recombination map size for Nasonia based on the hybrid mapping population.
Similar analyses were conducted for all other populations, individually as well as combined together, using the HapMap combined recombination map (hapMapRelease24CombinedRecombMap).
To investigate recombination patterns across genomic regions, maps describing historic LD levels were constructed for each chromosome based on population recombination rate in the NRF data.
The chicken recombination map from Groenen et al. (2009) is based on SNPs across three mapping populations.
Similarly the combined HapMap recombination map (hapMapRelease24CombinedRecombMap) was used to identify recombination hotspots and coldspots for all other populations [ 6, 33, 34].We studied the genomic distribution of the recombination rates from the YRI-specific map and the genomic regions corresponding to the top 1% recombination rates were defined as recombination hotspots for YRI.
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