Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees.
By Feng-Chi Chen, Wen-Hsiung Li. American Journal of Human Genetics, 2001
732 citations recorded by the source corpus.
Subfields: Genetics, Plant Science
View Paper: https://www.semanticscholar.org/paper/a6f6738f350f33e7c4d0e0f6d2389c345c206a34
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Citations in the corpus
- Species trees from gene trees: reconstructing Bayesian posterior distributions of a species phylogeny using estimated gene tree distributions. (2007, background): “…extinction rate (e), and the number of species (n), the joint density of the topology (T) and branch lengths (T) of a particular species tree is (Yang and Rannala, 1997): Mutation rate variation among loci may influence the estimation of ancestral population sizes (Yang, 1997; Chen and Li, 2001).”
- Discordance of Species Trees with Their Most Likely Gene Trees (2006, unknown): “When many loci are studied, the species tree topology is often estimated using the most frequently inferred gene tree topology [1–5].”
- Bayes estimation of species divergence times and ancestral population sizes using DNA sequences from multiple loci. (2003, methodology): “Those estimates seem the data set of Chen and Li (2001) at 53 loci and then too young, as current opinion appears to favor a date including the data at the three other loci as well, in as old as 7 MY (Brunet et al. 2002).”
- A common inversion under selection in Europeans (2005, background): “Assuming that the split between humans and chimpanzees occurred ∼6 million years ag”
- New Genetic Evidence on the Evolution of Chimpanzee Populations and Implications for Taxonomy (2006, background): “Several studies suggest that chimpanzees, whose genome is remarkably similar to our own (Chen and Li, 2001; Wildman et al., 2003), possess 2–6 times the genetic diversity of humans (Kaessmann et al.”
- Multilocus Methods for Estimating Population Sizes, Migration Rates and Divergence Time, With Applications to the Divergence of Drosophila pseudoobscura and D. persimilis (2004, background): “The model can also be simpli- chimpanzees [i.e., assuming 6 million years divergence, at 25 years per generation (Chen and Li 2001; Brunetfied, and the number of parameters reduced, by speci- fying that two or all three population mutation rates are et al. 2002)].”
- Widespread Genomic Signatures of Natural Selection in Hominid Evolution (2009, background): “At such positions, the human-chimpanzee coalescent predates the gorilla split [29] (see Figure S1) and so is very old.”
- Variation in genome-wide mutation rates within and between human families (2011, background): “These apparently discordant estimates can be largely reconciled if the age of the human-chimpanzee divergence is pushed back to 7 million years, as suggested by some interpretations of recent fossil find”
- Comparing the human and chimpanzee genomes: Searching for needles in a haystack (2005, background): “Humans (Homo sapiens) and chimpanzees (Pan troglodytes) last shared a common ancestor ∼5–7 million years ago (Mya) (Chen and Li 2001; Brunet et al. 2002).”
- Ultraconserved elements anchor thousands of genetic markers spanning multiple evolutionary timescales. (2012, background): “Our results from primates indicate that UCEs have levels of gene-tree discordance similar to those expected by coalescent stochasticity at the well-described divergence between human, chimpanzees, and gorillas (Chen and Li 2001).”