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Articles tagged G3 Journal
(234 results)
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New in G3: mutagenic CpGs, maternal mice, and multi-trait mapping
Check out the January issue of G3! Investigations Genomic Prediction Accounting for Residual Heteroskedasticity Zhining Ou, Robert J. Tempelman, Juan P. Steibel, Catherine W. Ernst, Ronald O. Bates, and Nora M. Bello G3 January 2016 6:1-13; Early Online November 12, 2015, doi:10.1534/g3.115.022897 Abstract | Full Text | Full Text (PDF) | Supporting Information Comparative Genomics…
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Fungal signaling illuminated by undergrad researchers
Versatile and ubiquitous, G-protein coupled receptors (GPCRs) are the busybodies of eukaryotic signaling. This diverse group of stimulus-sensing membrane proteins are involved in countless aspects of growth, development, immunity, metabolism, and response to environmental conditions. In the latest issue of G3, Cabrera et al. report phenotypic and gene expression data for more than 80% of…
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G3 Editor-in-Chief named to Order of Canada
Brenda Andrews, Editor-in-Chief of the GSA journal G3: Genes|Genomes|Genetics, has been named Companion to the Order of Canada, one of the country’s highest civilian honors. Established in 1967 by Her Majesty Queen Elizabeth II, selection to the Order recognizes outstanding achievement, dedication to the community, and service to the nation. Companion to the Order of Canada is…
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New in G3: POPSEQ in wheat, strawberry sex determination, and germline genes in the Jewel Wasp
Check out the December issue of G3! Meeting Report Meeting Report: Fungal Genomics Meets Social Media: Highlights of the 28th Fungal Genetics Conference at Asilomar Michelle Momany, Antonio Di Pietro, William G. Alexander, Bridget M. Barker, Omar S. Harb, Sophien Kamoun, Francis Martin, J. Chris Pires, Jason E Stajich, Bart P. H. J. Thomma, and…
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Frog fungus gets lazy in the lab
Amphibians around the world have been devastated by the spread of the deadly fungus Batrachochytrium dendrobatidis (Bd). But although many populations have been decimated, others have survived the same threat. One reason for such different outcomes is variation in virulence between Bd isolates. In the latest issue of G3, Refsnider and Poorten et al. investigate…
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New in G3: association mapping, amino acid usage, and appendage development
Check out the October issue of G3! Meeting Report Meeting Report on the Challenge of Inference from Genome to Phenome Bevan Emma Huang, Antonio Reverter, Ian Purvis, and Scott Chapman G3 October 2015 5:1945-1947; doi:10.1534/g3.115.019182 Full Text | Full Text (PDF) | Supporting Information Investigations Endogenous Small RNA Mediates Meiotic Silencing of a Novel DNA Transposon…
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Exome sequencing: Giving researchers more bang for their buck
Over the last decade, advances in next-generation sequencing technology have given rise to many findings increasing our understanding of human disease and natural variation within species. Sequencing of the exome, the small fraction of the genome encompassing all exons of protein coding genes, has gained popularity as an inexpensive alternative to sequencing the entire genome.…
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New in G3: transcriptomics, temperature-sensitive yeast, and TALENs
Check out the September issue of G3! Investigations SWEEP: A Tool for Filtering High-Quality SNPs in Polyploid Crops Josh P. Clevenger and Peggy Ozias-Akins G3 September 2015 5:1797-1803; Early Online July 6, 2015, doi:10.1534/g3.115.019703 Abstract | Full Text | Full Text (PDF) | Supporting Information Comparative Transcriptome Analysis of the Cosmopolitan Marine Fungus Corollospora maritima Under Two…
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Members of GSA community elected to ASHG Board
Two members of the GSA community have been elected to the Board of Directors of GSA’s sister society, the American Society of Human Genetics (ASHG): Nicholas Katsanis, PhD Jean and George R. Brumley Professor of Cell Biology and Pediatrics Director, Center for Human Disease Modeling Duke University School of Medicine Associate Editor, G3: Genes|Genomes|Genetics Sarah…
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Speeding up PCD diagnosis with whole-exome sequencing
Primary ciliary dyskinesia (PCD) is a disorder characterized by chronic respiratory distress that has a history of going undiagnosed. Combined whole-exome sequencing (WES) and copy-number variant (CNV) analysis can aid in diagnosing patients with PCD, according to research published in G3 this month. PCD arises from mutations in cilia-associated genes—and results from the paralysis of…
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New in G3: CRISPR, C. elegans, & a ciliopathy
Check out the August issue of G3! Perspectives Exome Sequencing: Current and Future Perspectives Amanda Warr, Christelle Robert, David Hume, Alan Archibald, Nader Deeb, and Mick Watson G3 August 2015 5:1543-1550; Early Online July 2, 2015, doi:10.1534/g3.115.018564 Full Text | Full Text (PDF) Investigations Identification of Wnt Pathway Target Genes Regulating the Division and Differentiation of…