The genomic evolution and causes of phenotypic variation among humans and great apes remain largely unknown, although the phylogenetic relationships among them have been extensively explored. Previous studies that focus on differences at the amino acid and nucleotide sequence levels have revealed a high degree of similarity between humans and chimpanzees, suggesting that other types of genomic change may have contributed to the relatively large phenotypic differences between them. For example, the activity of long interspersed element 1 (LINE-1) retrotransposons may impose significant changes on genomic structure and function and, consequently, on phenotype. Here we investigate the relative rates of LINE-1 amplification in the lineages lead...
Genetic studies of human evolution require high-quality contiguous ape genome assemblies that are no...
Although data on nucleotide sequence variation in the human nuclear genome have begun to accumulate,...
Copy number variation (CNV) contributes to the genetic basis of disease and has significantly restru...
The genomic evolution and causes of phenotypic variation among humans and great apes remain largely ...
The long interspersed element-1 (LINE-1 or L1) is a highly successful retrotransposon in mammals. L1...
Cataloged from PDF version of article.We analyzed 83 fully sequenced great ape genomes for mobile el...
The L1 Ta subfamily of long interspersed elements (LINEs) consists exclusively of human-specific L1 ...
We analyzed 83 fully sequenced great ape genomes for mobile element insertions, discovering a total ...
Identifying cellular and molecular differences between human and non-human primates (NHPs) is essent...
The primate order is a monophyletic group thought to have diverged from the Euarchonta more than 65 ...
The long interspersed element-1 (LINE-1 or L1) and Alu elements are the most abundant mobile element...
AbstractAnalysis of the human genome suggests novel genes created by retroposition may play an impor...
Transposable genetic elements are abundant in the genomes of most organisms, including humans. These...
The total numbers of copies of two repeat families, L1 (Kpn I) and Alu, have been measured in the DN...
This work focuses on the distribution of LINE-1 (a Long Interspersed Nuclear Element) in primates an...
Genetic studies of human evolution require high-quality contiguous ape genome assemblies that are no...
Although data on nucleotide sequence variation in the human nuclear genome have begun to accumulate,...
Copy number variation (CNV) contributes to the genetic basis of disease and has significantly restru...
The genomic evolution and causes of phenotypic variation among humans and great apes remain largely ...
The long interspersed element-1 (LINE-1 or L1) is a highly successful retrotransposon in mammals. L1...
Cataloged from PDF version of article.We analyzed 83 fully sequenced great ape genomes for mobile el...
The L1 Ta subfamily of long interspersed elements (LINEs) consists exclusively of human-specific L1 ...
We analyzed 83 fully sequenced great ape genomes for mobile element insertions, discovering a total ...
Identifying cellular and molecular differences between human and non-human primates (NHPs) is essent...
The primate order is a monophyletic group thought to have diverged from the Euarchonta more than 65 ...
The long interspersed element-1 (LINE-1 or L1) and Alu elements are the most abundant mobile element...
AbstractAnalysis of the human genome suggests novel genes created by retroposition may play an impor...
Transposable genetic elements are abundant in the genomes of most organisms, including humans. These...
The total numbers of copies of two repeat families, L1 (Kpn I) and Alu, have been measured in the DN...
This work focuses on the distribution of LINE-1 (a Long Interspersed Nuclear Element) in primates an...
Genetic studies of human evolution require high-quality contiguous ape genome assemblies that are no...
Although data on nucleotide sequence variation in the human nuclear genome have begun to accumulate,...
Copy number variation (CNV) contributes to the genetic basis of disease and has significantly restru...