Ecological Genetics and Genomics publishes ecological studies of broad interest that provide significant insight into ecological interactions or/ and species diversification. New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologie...
Here, the authors conduct an epigenome-wide association study, finding that clonal hematopoiesis caused by DNMT3A vs. TET2 mutations has directionally opposing changes in DNA methylation profiles, with both promoting stem cell self-renewal. M d Mesbah Uddin Ngoc Quynh H. Nguyen Karen N. Conneely...
Increasing acceptance that evolution can be ‘rapid’ (or ‘contemporary’) has generated growing interest in the consequences for ecology. The genetics and genomics of these ‘eco-evolutionary dynamics’ will be—to a large extent—the genetics and genomics of organismal phenotypes. In the hope of...
Today, the notion of cancer being a consequence of genetic alterations, is almost intuitive and the advances in molecular biology and genomics have given us many tools to understand and possibly to combat cancer. Since science has always existed in a continuum, the genetic alterations in cancer ...
FASSO: Functional Annotations using Sequence and Structure Orthology - GitHub - Maize-Genetics-and-Genomics-Database/FASSO: FASSO: Functional Annotations using Sequence and Structure Orthology
ELSEVIERBrenners Encyclopedia of Genetics
Please give credit and cite the MutationalPatterns R Package when you use it for your data analysis. A paper for the newest version of the package is published inBMC Genomics. The original MutationalPatterns paper is published inGenome Medicine. ...
SARS-CoV-2 virus belongs to the B lineage of the β-coronaviruses (β-CoVs); this family comprises an enveloped, non-segmented, positive-sense single-stranded RNA virus genome, with a 5′ cap structure and 3′ poly-A tail, allowing to perform as an mRNA for translation of the replicase...
HomeSOPHiA DDM™ for GenomicsInherited DisordersPharmacogenomics Accurate CNV detection CNVs are accurately detected by our MUSKAT™algorithm alongside SNVs and Indels in a single experiment capable of detecting known and previously undetected variants. ...
doi:10.1016/j.tig.2022.06.003PubMedGoogle ScholarCrossref See More About Genetics and Genomics Pediatrics open access Trending Clinical Variant Reclassification in Hereditary Disease Genetic Testing Research November 6, 2024 National Rapid Genome Sequencing in Neonatal Intensive Care Research February 22, ...