[HTML][HTML] Alu elements: know the SINEs
P Deininger - Genome biology, 2011 - Springer
Alu elements: know the SINEs | Genome Biology Skip to main content SpringerLink Account
Menu Find a journal Publish with us Track your research Search Cart 1.Home 2.Genome …
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Copy number variation in human health, disease, and evolution
Copy number variation (CNV) is a source of genetic diversity in humans. Numerous CNVs
are being identified with various genome analysis platforms, including array comparative …
are being identified with various genome analysis platforms, including array comparative …
Dynamics of genome size evolution in birds and mammals
A Kapusta, A Suh, C Feschotte - Proceedings of the …, 2017 - National Acad Sciences
Genome size in mammals and birds shows remarkably little interspecific variation compared
with other taxa. However, genome sequencing has revealed that many mammal and bird …
with other taxa. However, genome sequencing has revealed that many mammal and bird …
LINE-1 elements in structural variation and disease
CR Beck, JL Garcia-Perez, RM Badge… - Annual review of …, 2011 - annualreviews.org
The completion of the human genome reference sequence ushered in a new era for the
study and discovery of human transposable elements. It now is undeniable that …
study and discovery of human transposable elements. It now is undeniable that …
Mobile elements create structural variation: analysis of a complete human genome
Structural variants (SVs) are common in the human genome. Because approximately half of
the human genome consists of repetitive, transposable DNA sequences, it is plausible that …
the human genome consists of repetitive, transposable DNA sequences, it is plausible that …
Transposable elements: powerful facilitators of evolution
Transposable elements (TEs) are powerful facilitators of genome evolution, and hence of
phenotypic diversity as they can cause genetic changes of great magnitude and variety. TEs …
phenotypic diversity as they can cause genetic changes of great magnitude and variety. TEs …
[HTML][HTML] A human genome structural variation sequencing resource reveals insights into mutational mechanisms
Understanding the prevailing mutational mechanisms responsible for human genome
structural variation requires uniformity in the discovery of allelic variants and precision in …
structural variation requires uniformity in the discovery of allelic variants and precision in …
[HTML][HTML] Differences between human and chimpanzee genomes and their implications in gene expression, protein functions and biochemical properties of the two …
MV Suntsova, AA Buzdin - BMC genomics, 2020 - Springer
Chimpanzees are the closest living relatives of humans. The divergence between human
and chimpanzee ancestors dates to approximately 6, 5–7, 5 million years ago. Genetic …
and chimpanzee ancestors dates to approximately 6, 5–7, 5 million years ago. Genetic …
Complex human chromosomal and genomic rearrangements
Copy number variation (CNV) is a major source of genetic variation among humans. In
addition to existing as benign polymorphisms, CNVs can also convey clinical phenotypes …
addition to existing as benign polymorphisms, CNVs can also convey clinical phenotypes …
Transposable elements as drivers of genomic and biological diversity in vertebrates
Comparative genomics has revealed that major vertebrate lineages contain quantitatively
and qualitatively different populations of retrotransposable elements and DNA transposons …
and qualitatively different populations of retrotransposable elements and DNA transposons …