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G3: Genes|Genomes|Genetics is a peer-reviewed journal published by Oxford University Press, covering Genetic Mapping and Diversity in Plants and Animals, Genetic and phenotypic traits in livestock, Genomics and Phylogenetic Studies. Over its lifetime it has published 4,829 papers, which have received 124,404 citations.
| Publisher | Oxford University Press |
|---|---|
| Reference style | Author–year (OUP) Author–year — (Smith, 2023) in the text Smith, A., Jones, B. and Lee, C. (2023) 'A representative article title', G3: Genes|Genomes|Genetics, 12(3), pp. 45–58.
Formats any DOI in the closest standard style — G3: Genes|Genomes|Genetics has no published style definition, so this is an approximation. No sign-up. |
| Publishes research in | Genetic Mapping and Diversity in Plants and Animals Genetic and phenotypic traits in livestock Genomics and Phylogenetic Studies CRISPR and Genetic Engineering Genetics, Aging, and Longevity in Model Organisms |
| ISSN | 2160-1836 |
| Citation impact (2-yr) | 2.68 |
| h-index | 120 |
| i10-index | 2,820 |
| Article processing charge | $2,400 |
| Open access | Yes — indexed in DOAJ |
| Top institutions publishing here | Agricultural Research Service |
| Journal website | www.g3journal.org |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Reconstruction of target genomes from sequence data produced by instruments that are agnostic as to the species-of-origin may be confounded by contaminant DNA. Whether introduced during sample processing or through co-extraction alongside the target DNA, if insufficient care is taken during the assembly process, the final assembled genome may be a mixture of data from…
Advances in sequencing technology provide special opportunities for genotyping individuals with speed and thrift, but the lack of software to automate the calling of tens of thousands of genotypes over hundreds of individuals has hindered progress. Stacks is a software system that uses short-read sequence data to identify and genotype loci in a set of…
Genotype imputation is a statistical technique that is often used to increase the power and resolution of genetic association studies. Imputation methods work by using haplotype patterns in a reference panel to predict unobserved genotypes in a study dataset, and a number of approaches have been proposed for choosing subsets of reference haplotypes that will…
The adaptation of CRISPR/SpCas9 technology to mammalian cell lines is transforming the study of human functional genomics. Pooled libraries of CRISPR guide RNAs (gRNAs) targeting human protein-coding genes and encoded in viral vectors have been used to systematically create gene knockouts in a variety of human cancer and immortalized cell lines, in an effort to…
The genome of the budding yeast Saccharomyces cerevisiae was the first completely sequenced from a eukaryote. It was released in 1996 as the work of a worldwide effort of hundreds of researchers. In the time since, the yeast genome has been intensively studied by geneticists, molecular biologists, and computational scientists all over the world. Maintenance…
