ReviewFEMS yeast research2026
From one genome to thousands, and beyond.
Review in FEMS yeast research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Over the past three decades, Saccharomyces cerevisiae has gone from being the first eukaryote to have its genome fully sequenced to one of the most studied biological systems. Advances in sequencing technologies, functional genomics, and population genomics have expanded the scope of study from a single laboratory reference genome to thousands of natural isolates, and the species-wide pangenome. These advances have revealed vast genetic and structural diversity, shaped by evolution, ecology, and domestication, while large-scale experimental resources have made yeast a model organism of choice in systems biology. In this review, we trace this transition from a reference genome view to an understanding of diversity at the population level, highlighting how telomere-to-telomere assemblies, graph-pangenome, and multi-omics approaches are transforming our ability to link genomic variation to phenotype. Together, these advances place S. cerevisiae at the forefront of efforts to understand and predict genotype-phenotype relationships in eukaryotes.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.