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Rapid evolution of fine-scale recombination during domestication: a perspective from population genomics

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inferredcites →https://doi.org/10.1007/bf00328866openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ajhg.2022.12.010openalex-snapshot
Fast, accurate local ancestry inference with FLARE
inferredcites →https://doi.org/10.1016/j.cell.2016.09.035openalex-snapshot
The Landscape of Mouse Meiotic Double-Strand Break Formation, Processing, and Repair
inferredcites →https://doi.org/10.1016/j.cub.2010.01.048openalex-snapshot
Meiosis: A PRDM9 Guide to the Hotspots of Recombination
inferredcites →https://doi.org/10.1016/j.gde.2016.09.006openalex-snapshot
The impact of recent population history on the deleterious mutation load in humans and close evolutionary relatives
inferredcites →https://doi.org/10.1016/j.tig.2013.01.003openalex-snapshot
A population genetics view of animal domestication
inferredcites →https://doi.org/10.1016/j.tig.2017.03.003openalex-snapshot
Variation in Recombination Rate: Adaptive or Not?
inferredcites →https://doi.org/10.1038/nature06258openalex-snapshot
A second generation human haplotype map of over 3.1 million SNPs
inferredcites →https://doi.org/10.1038/nature10336openalex-snapshot
The landscape of recombination in African Americans
inferredcites →https://doi.org/10.1038/nature11089openalex-snapshot
Genetic recombination is directed away from functional genomic elements in mice
inferredcites →https://doi.org/10.1038/nature12961openalex-snapshot
The genomic landscape of Neanderthal ancestry in present-day humans
inferredcites →https://doi.org/10.1038/ng.2309openalex-snapshot
Comparative population genomics of maize domestication and improvement
inferredcites →https://doi.org/10.1038/ng.3199openalex-snapshot
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inferredcites →https://doi.org/10.1038/nrg2712openalex-snapshot
Mammalian recombination hot spots: properties, control and evolution
inferredcites →https://doi.org/10.1038/s41422-020-0349-yopenalex-snapshot
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inferredcites →https://doi.org/10.1038/s41576-020-0240-1openalex-snapshot
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inferredcites →https://doi.org/10.1038/s41586-020-2347-0openalex-snapshot
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inferredcites →https://doi.org/10.1038/s42003-019-0445-zopenalex-snapshot
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inferredcites →https://doi.org/10.1038/s42003-020-1116-9openalex-snapshot
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inferredcites →https://doi.org/10.1073/pnas.1319032110openalex-snapshot
Fine-scale variation in meiotic recombination in Mimulus inferred from population shotgun sequencing
inferredcites →https://doi.org/10.1073/pnas.1323964111openalex-snapshot
Current perspectives and the future of domestication studies
inferredcites →https://doi.org/10.1073/pnas.2022805118openalex-snapshot
A simple expression for the strength of selection on recombination generated by interference among mutations
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Microchromosomes are building blocks of bird, reptile, and mammal chromosomes
inferredcites →https://doi.org/10.1073/pnas.2205785119openalex-snapshot
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inferredcites →https://doi.org/10.1086/380606openalex-snapshot
The Evolution of Recombination under Domestication: A Test of Two Hypotheses
inferredcites →https://doi.org/10.1086/519795openalex-snapshot
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
inferredcites →https://doi.org/10.1093/bioinformatics/btac234openalex-snapshot
Deep learning identifies and quantifies recombination hotspot determinants
inferredcites →https://doi.org/10.1093/bioinformatics/btr330openalex-snapshot
The variant call format and VCFtools
inferredcites →https://doi.org/10.1093/bioinformatics/btu170openalex-snapshot
Trimmomatic: a flexible trimmer for Illumina sequence data
inferredcites →https://doi.org/10.1093/bioinformatics/bty875openalex-snapshot
PopLDdecay: a fast and effective tool for linkage disequilibrium decay analysis based on variant call format files
inferredcites →https://doi.org/10.1093/dnares/dsx024openalex-snapshot
Low-coverage resequencing detects meiotic recombination pattern and features in tomato RILs
inferredcites →https://doi.org/10.1093/genetics/147.2.879openalex-snapshot
The Evolution of Recombination: Removing the Limits to Natural Selection
inferredcites →https://doi.org/10.1093/genetics/156.1.423openalex-snapshot
The Evolution of Recombination in a Heterogeneous Environment
inferredcites →https://doi.org/10.1093/genetics/iyab229openalex-snapshot
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inferredcites →https://doi.org/10.1093/molbev/msaa038openalex-snapshot
Predicting the Landscape of Recombination Using Deep Learning
inferredcites →https://doi.org/10.1093/molbev/msaa113openalex-snapshot
Ancient Hybridization with an Unknown Population Facilitated High-Altitude Adaptation of Canids
inferredcites →https://doi.org/10.1093/molbev/msab287openalex-snapshot
Domestication Shapes Recombination Patterns in Tomato
inferredcites →https://doi.org/10.1093/molbev/msac066openalex-snapshot
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inferredcites →https://doi.org/10.1093/molbev/msac200openalex-snapshot
The Genomic Landscapes of Desert Birds Form over Multiple Time Scales
inferredcites →https://doi.org/10.1093/molbev/msac267openalex-snapshot
Rapid Evolution of the Fine-scale Recombination Landscape in Wild House Mouse ( Mus musculus ) Populations
inferredcites →https://doi.org/10.1093/molbev/msu211openalex-snapshot
selscan: An Efficient Multithreaded Program to Perform EHH-Based Scans for Positive Selection
inferredcites →https://doi.org/10.1093/molbev/msu269openalex-snapshot
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inferredcites →https://doi.org/10.1093/molbev/msu322openalex-snapshot
Strong Artificial Selection in Domestic Mammals Did Not Result in an Increased Recombination Rate
inferredcites →https://doi.org/10.1093/molbev/msv011openalex-snapshot
Functional Organization of the Genome May Shape the Species Boundary in the House Mouse
inferredcites →https://doi.org/10.1093/molbev/msv194openalex-snapshot
The Mosaic Ancestry of the Drosophila Genetic Reference Panel and the D. melanogaster Reference Genome Reveals a Network of Epistatic Fitness Interactions
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The Time Scale of Recombination Rate Evolution in Great Apes
inferredcites →https://doi.org/10.1093/molbev/msy126openalex-snapshot
Loter: A Software Package to Infer Local Ancestry for a Wide Range of Species
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inferredcites →https://doi.org/10.1093/molbev/msz141openalex-snapshot
Variation in Recombination Rate Is Shaped by Domestication and Environmental Conditions in Barley
inferredcites →https://doi.org/10.1093/nar/gkad347openalex-snapshot
g:Profiler—interoperable web service for functional enrichment analysis and gene identifier mapping (2023 update)
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Local Rates of Recombination Are Positively Correlated with GC Content in the Human Genome
inferredcites →https://doi.org/10.1093/sysbio/syw037openalex-snapshot
Terrace Aware Data Structure for Phylogenomic Inference from Supermatrices
inferredcites →https://doi.org/10.1098/rstb.2016.0455openalex-snapshot
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inferredcites →https://doi.org/10.1101/gr.086538.108openalex-snapshot
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inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1101/gr.124123.111openalex-snapshot
Death of PRDM9 coincides with stabilization of the recombination landscape in the dog genome
inferredcites →https://doi.org/10.1101/gr.243311.118openalex-snapshot
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inferredcites →https://doi.org/10.1101/gr.277414.122openalex-snapshot
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inferredcites →https://doi.org/10.1105/tpc.18.00750openalex-snapshot
Historical Meiotic Crossover Hotspots Fueled Patterns of Evolutionary Divergence in Rice
inferredcites →https://doi.org/10.1111/j.1095-8312.1983.tb01598.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/tpj.13262openalex-snapshot
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The Fine-Scale Structure of Recombination Rate Variation in the Human Genome
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Comparison of Fine-Scale Recombination Rates in Humans and Chimpanzees
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A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome
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A Fine-Scale Chimpanzee Genetic Map from Population Sequencing
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Nonparadoxical evolutionary stability of the recombination initiation landscape in yeast
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Stable recombination hotspots in birds
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Natural selection interacts with recombination to shape the evolution of hybrid genomes
inferredcites →https://doi.org/10.1126/science.aau1043openalex-snapshot
Characterizing mutagenic effects of recombination through a sequence-level genetic map
inferredcites →https://doi.org/10.1126/science.adj7026openalex-snapshot
Patterns of recombination in snakes reveal a tug-of-war between PRDM9 and promoter-like features
inferredcites →https://doi.org/10.1136/jech.2006.052969openalex-snapshot
Income inequality measures: Figure 1
inferredcites →https://doi.org/10.1186/s12711-016-0221-1openalex-snapshot
Effect of manipulating recombination rates on response to selection in livestock breeding programs
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inferredcites →https://doi.org/10.1186/s12864-017-3776-5openalex-snapshot
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inferredcites →https://doi.org/10.1186/s12915-021-01052-xopenalex-snapshot
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Selection shapes the landscape of functional variation in wild house mice
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inferredcites →https://doi.org/10.1371/journal.pgen.1004790openalex-snapshot
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inferredcites →https://doi.org/10.1371/journal.pgen.1007741openalex-snapshot
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inferredcites →https://doi.org/10.1534/genetics.112.141036openalex-snapshot
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Crossover Heterogeneity in the Absence of Hotspots in Caenorhabditis elegans
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Chicken chromatin accessibility atlas accelerates epigenetic annotation of birds and gene fine-mapping associated with growth traits
inferredcites →https://doi.org/10.3389/fpls.2011.00012openalex-snapshot
Phenotype Uniformity in Combined-Stress Environments has a Different Genetic Architecture than in Single-Stress Treatments
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Immune genes are hotspots of shared positive selection across birds and mammals
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