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J. Large DNA palindromes as a common form of structural chromosome aberrations in human cancers. Hum. Cell 19, 17–23 (2006). PubMed Google Scholar Coquelle, A., Pipiras, E., Toledo, F., Buttin, G. & Debatisse, M. Expression of fragile sites triggers intrachromosomal mammalian ...
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Known risk loci for endometrial cancer explain approximately one third of familial endometrial cancer. However, the association of germline copy number var
The chicken (Gallus gallus) is an important model organism that bridges the evolutionary gap between mammals and other vertebrates. Copy number variations (CNVs) are a form of genomic structural variation widely distributed in the genome. CNV analysis ha
Somatic copy number alterations (CNAs) are major mutations that contribute to the development and progression of various cancers. Despite a few computational methods proposed to detect CNAs from single-cell transcriptomic data, the technical sparsity of
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the two rice subspecies,indicaandjaponica, did not form separate clusters. This result might be an artifact of the measurements being based on a common reference sample (Nipponbare), or the CNVs may be less phylogenetically reliable than neutral markers by reason of stronger selective constraints [...
(Helentrons) Jainy Thomas1, Komal Vadnagara2 and Ellen J Pritham1* Abstract Background: The Drosophila INterspersed Elements-1 (DINE-1/INE1) transposable elements (TEs) are the most abundant component of the Drosophila melanogaster genome and have been associated with functional gene duplications....