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Exploiting homologous recombination increases SATAY efficiency for loss- and gain-of-function screening
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0061(199807)14:10<953::aid-yea293>3.0.co;2-uopenalex-snapshot
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1002/(sici)1097-0061(199812)14:16<1471::aid-yea353>3.0.co;2-yopenalex-snapshot
Biochemistry, cell biology and molecular biology of lipids ofSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1002/yea.1142openalex-snapshot
A versatile toolbox for PCR‐based tagging of yeast genes: new fluorescent proteins, more markers and promoter substitution cassettes
inferredcites →https://doi.org/10.1006/plas.1997.1305openalex-snapshot
Minimum Length of Sequence Homology Required forin VivoCloning by Homologous Recombination in Yeast
inferredcites →https://doi.org/10.1007/s004380050975openalex-snapshot
YAP1 confers resistance to the fatty acid synthase inhibitor cerulenin through the transporter Flr1p in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/0048-3575(73)90100-4openalex-snapshot
Mechanism of action and fate of the fungicide chlorothalonil (2,4,5,6-tetrachloroisophthalonitrile) in biological systems
inferredcites →https://doi.org/10.1016/0092-8674(89)90584-9openalex-snapshot
Elevated recombination rates in transcriptionally active DNA
inferredcites →https://doi.org/10.1016/c2009-0-01952-7openalex-snapshot
Guide to Yeast Genetics: Functional Genomics, Proteomics, and Other Systems Analysis
inferredcites →https://doi.org/10.1016/j.bbamcr.2014.10.006openalex-snapshot
Assembly of β-barrel proteins in the mitochondrial outer membrane
inferredcites →https://doi.org/10.1016/j.micres.2013.11.004openalex-snapshot
High-resolution chemical dissection of a model eukaryote reveals targets, pathways and gene functions
inferredcites →https://doi.org/10.1016/j.molcel.2013.09.026openalex-snapshot
Genome-wide Consequences of Deleting Any Single Gene
inferredcites →https://doi.org/10.1016/s1097-2765(02)00696-2openalex-snapshot
The FAD- and O2-Dependent Reaction Cycle of Ero1-Mediated Oxidative Protein Folding in the Endoplasmic Reticulum
inferredcites →https://doi.org/10.1038/82827openalex-snapshot
Transposition of maize Ac/Ds transposable elements in the yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1038/msb.2011.58openalex-snapshot
The essential genome of a bacterium
inferredcites →https://doi.org/10.1038/nature00935openalex-snapshot
Functional profiling of the Saccharomyces cerevisiae genome
inferredcites →https://doi.org/10.1038/nature07728openalex-snapshot
Bidirectional promoters generate pervasive transcription in yeast
inferredcites →https://doi.org/10.1038/nmeth.1377openalex-snapshot
Tn-seq: high-throughput parallel sequencing for fitness and genetic interaction studies in microorganisms
inferredcites →https://doi.org/10.1038/nmeth.1401openalex-snapshot
An auxin-based degron system for the rapid depletion of proteins in nonplant cells
inferredcites →https://doi.org/10.1038/s41598-018-28217-zopenalex-snapshot
Genome-Wide Determination of Gene Essentiality by Transposon Insertion Sequencing in Yeast Pichia pastoris
inferredcites →https://doi.org/10.1073/pnas.1820915116openalex-snapshot
Complex modifier landscape underlying genetic background effects
inferredcites →https://doi.org/10.1074/jbc.m504716200openalex-snapshot
Oxidant-specific Folding of Yap1p Regulates Both Transcriptional Activation and Nuclear Localization
inferredcites →https://doi.org/10.1093/emboj/16.7.1710openalex-snapshot
Regulation of yAP‐1 nuclear localization in response to oxidative stress
inferredcites →https://doi.org/10.1093/genetics/162.3.1091openalex-snapshot
High-Resolution Genetic Mapping With Ordered Arrays of Saccharomyces cerevisiae Deletion Mutants
inferredcites →https://doi.org/10.1093/nar/24.23.4639openalex-snapshot
Identification of a Saccharomyces cerevisiae Ku80 homologue: roles in DNA double strand break rejoining and in telomeric maintenance
inferredcites →https://doi.org/10.1101/575860openalex-snapshot
The Aspartic Protease Ddi1 Contributes to DNA-Protein Crosslink Repair in Yeast
inferredcites →https://doi.org/10.1101/gr.232330.117openalex-snapshot
Transposon insertional mutagenesis in Saccharomyces uvarum reveals trans -acting effects influencing species-dependent essential genes
inferredcites →https://doi.org/10.1128/mbio.02048-18openalex-snapshot
Gene Essentiality Analyzed by In Vivo Transposon Mutagenesis and Machine Learning in a Stable Haploid Isolate of Candida albicans
inferredcites →https://doi.org/10.1128/mcb.24.3.1351-1364.2004openalex-snapshot
Microhomology-Dependent End Joining and Repair of Transposon-Induced DNA Hairpins by Host Factors in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1371/journal.pbio.2005129openalex-snapshot
In vivo insertion pool sequencing identifies virulence factors in a complex fungal–host interaction
inferredcites →https://doi.org/10.1371/journal.pgen.0030154openalex-snapshot
A Comprehensive Genetic Characterization of Bacterial Motility
inferredcites →https://doi.org/10.1534/g3.117.040022openalex-snapshot
Whole-Genome Sequence and Variant Analysis of W303, a Widely-Used Strain of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1534/genetics.112.139642openalex-snapshot
A Hyperactive Transposase of the Maize Transposable ElementActivator(Ac)
inferredcites →https://doi.org/10.1534/genetics.113.152744openalex-snapshot
Integration Profiling of Gene Function With Dense Maps of Transposon Integration
inferredcites →https://doi.org/10.1534/genetics.114.161620openalex-snapshot
The Yeast Deletion Collection: A Decade of Functional Genomics
inferredcites →https://doi.org/10.1534/genetics.118.300981openalex-snapshot
HermesTransposon Mutagenesis Shows [URE3] Prion Pathology Prevented by a Ubiquitin-Targeting Protein: Evidence for Carbon/Nitrogen Assimilation Cross Talk and a Second Function for Ure2p inSaccharomyces cerevisiae
inferredcites →https://doi.org/10.7554/elife.23570openalex-snapshot
Functional mapping of yeast genomes by saturated transposition
inferredcites →https://doi.org/10.7554/elife.32110openalex-snapshot
Functional genomics of lipid metabolism in the oleaginous yeast Rhodosporidium toruloides
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-1-0716-2257-5_20openalex-snapshot
SAturated Transposon Analysis in Yeast (SATAY) for Deep Functional Mapping of Yeast Genomes
inferred← citeshttps://doi.org/10.1007/978-3-031-75666-5_4openalex-snapshot
Recent Advances in High-Throughput Genetics in Fungi
inferred← citeshttps://doi.org/10.1016/j.gde.2022.101963openalex-snapshot
Exploring conditional gene essentiality through systems genetics approaches in yeast
inferred← citeshttps://doi.org/10.1038/s41556-023-01198-6openalex-snapshot
Malonyl-CoA is a conserved endogenous ATP-competitive mTORC1 inhibitor
inferred← citeshttps://doi.org/10.1038/s44319-026-00709-4openalex-snapshot
Global genetic rewiring during compensatory evolution in the yeast polarity network
inferred← citeshttps://doi.org/10.1101/2021.08.31.458362openalex-snapshot
Genome-wide identification of sexual-reproduction genes in fission yeast via transposon-insertion sequencing
inferred← citeshttps://doi.org/10.1101/2022.11.06.515351openalex-snapshot
Malonyl-CoA is an ancient physiological ATP-competitive mTORC1 inhibitor
inferred← citeshttps://doi.org/10.1101/2024.07.28.605507openalex-snapshot
Saturation transposon mutagenesis enables genome-wide identification of genes required for growth and fluconazole resistance in the human fungal pathogen Cryptococcus neoformans
inferred← citeshttps://doi.org/10.1101/2025.02.13.638058openalex-snapshot
Laboratory yeast strains are highly diverse in lipid metabolism
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009414openalex-snapshot
Indole-3-acetic acid is a physiological inhibitor of TORC1 in yeast
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010462openalex-snapshot
Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast
inferred← citeshttps://doi.org/10.1371/journal.pone.0312437openalex-snapshot
Saturated Transposon Analysis in Yeast as a one-step method to quantify the fitness effects of gene disruptions on a genome-wide scale
inferred← citeshttps://doi.org/10.15252/embj.2021109998openalex-snapshot
Rewiring phospholipid biosynthesis reveals resilience to membrane perturbations and uncovers regulators of lipid homeostasis
inferred← citeshttps://doi.org/10.3389/ffunb.2021.633876openalex-snapshot
Hijacking Transposable Elements for Saturation Mutagenesis in Fungi
inferred← citeshttps://doi.org/10.3390/jof9050565openalex-snapshot
Fungal Drug Response and Antimicrobial Resistance
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