SNF-CLIMEDIN: A Randomized Trial of Digital Support and Intervention in Patients With Advanced Non–Small Cell Lung Cancer. A Hellenic Cooperative Oncology Group Study Shallow whole-genome sequencing ...

Genetic ancestry plays a key role in determining the behavior of head and neck tumors and may help explain why African-American patients survive for half as long as their counterparts of European ...

With the release of 2025-26 Topps Basketball on the horizon, Topps recently announced another chase element of the product that collectors can look out for: a rare number variation parallel. The cards ...

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Copy number variations (CNVs) are a pervasive form of genomic variation that entail duplications or deletions of DNA segments ranging from kilobases to megabases. In animal genomes, CNVs contribute ...

The following is a summary of “Mitochondrial DNA copy number variation in asthma risk, severity, and exacerbations,” published in the April 2025 issue of Journal of Allergy and Clinical Immunology by ...

Recent pan-cancer analysis revealed the global pattern and potential aetiologies of copy number variation signatures in human cancers, particularly those derived from non-hematopoietic tissues. In ...

The main forms of human genomic variation are shown in Figure 1. These include SNPs, which are qualitative in nature and involve only a single nucleotide, and a family of genomic changes collectively ...

Copy number variation in large gene families is well characterized for plant resistance genes, but similar studies are rare in animals. The zebrafish (Danio rerio) has hundreds of NLR immune genes, ...

Senior and Reviewing Editor; Max Planck Institute for Biology Tübingen, Germany In the interests of transparency, eLife publishes the most substantive revision requests and the accompanying author ...