G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights.G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. As part of our mission to serve our communities, we've published thematic collections, including Genomic Prediction, Multiparental Populations, Genetics of Immunity, and Genetics of Sex. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by the Directory of Open Access Journals to journals that achieve a high level of openness, adhering to Best Practices and high publishing standards.More than just a publisher, the Genetics Society of America is mission-driven and places a high priority on responding to community needs. GENETICS and G3 have long been committed to supporting resources that serve scientists. We were the first journals to partner with Cold Spring Harbor Laboratories to enable seamless deposits of manuscripts from our submission systems straight into the preprint server bioRxiv, as well as from bioRxiv to GENETICS and G3, and we have accepted submissions posted for preprint servers since 2012. Articles feature links to model organism databases like SGD, FlyBase, and WormBase. We have also partnered with Overleaf to provide custom templates for authors who use LaTex, saving them time at submission. The annotation tool Remarq is available on both the GENETICS and G3 websites and allows for collaborative commenting and article sharing. Our latest collaboration with Figshare ensures that supplemental material and data files are permanently associated with an article—and that authors aren’t limited by file type or size when providing data that support their work. Early online publication means that research investigations are freely accessible and in PubMed within days of acceptance – which eliminates delays in discovering the latest science.

G3:基因、基因組、遺傳學為發表高質量的基礎研究提供了一個論壇，特別是那些產生有用的遺傳和基因組信息的研究，如基因組圖譜、單基因研究、全基因組關聯和QTL研究，以及基因組報告、突變體篩選、方法和技術進展。G3的編輯委員會認為，這些數據的迅速傳播是分析的必要基礎，從而導致機械的見解。G3由美國遺傳學學會出版，滿足遺傳學界快速審查和出版遺傳學各領域重要成果的迫切和日益增長的需要。G3提供了發布令人困惑的發現的機會，或者提供未發布的結果，由于缺乏潛在的高影響的發現，這些結果可能沒有提交審查和發布。作為我們服務社區使命的一部分，我們出版了專題合集，包括基因組預測、多父母群體、免疫遺傳學和性別遺傳學。G3獲得了DOAJ印章，這是開放獲取期刊認證的標志，由開放獲取期刊目錄授予遵循最佳實踐和高出版標準的高開放性期刊。美國遺傳學協會不僅僅是一個出版商，它還以使命為導向，高度重視對社區需求的響應。遺傳學和G3一直致力于支持為科學家服務的資源。我們是第一批與冷泉港實驗室合作的期刊，使我們的投稿系統能夠無縫地將稿件直接存入預印本服務器bioRxiv，以及從bioRxiv到遺傳學和G3。自2012年以來，我們已經接受了預印本服務器上的投稿。文章提供了到模型生物數據庫(如SGD、FlyBase和蟲庫)的鏈接。我們還與Overleaf合作，為使用LaTex的作者提供定制模板，節省了提交時的時間。注釋工具備注可在遺傳學和G3網站上使用，并允許協作評論和文章共享。我們與Figshare的最新合作確保了補充材料和數據文件與文章永久關聯，并且在提供支持其工作的數據時，作者不受文件類型或大小的限制。早期的在線出版意味著研究調查可以在公眾接受的幾天內免費訪問并在PubMed上發表——這消除了發現最新科學的延遲。