Evidence map›Paper›PMID 20923977›Full record

ArticleGenetics2010

Discovery of mutations in Saccharomyces cerevisiae by pooled linkage analysis and whole-genome sequencing.

Shanda R Birkeland, Natsuko Jin, Alev Cagla Ozdemir, Robert H Lyons, Lois S Weisman, Thomas E Wilson

Abstract read
In one paragraph

Article in Genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

51 citing papers in PubMed.

  1. Article
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  4. Review
  5. Article
  6. Anterior-posterior pattern formation in ciliates.The Journal of eukaryotic microbiology · 2022
    Review
  7. Article
  8. Article
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  12. Article
  13. Article
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  18. Article
  19. Article
  20. Whole-Genome Sequencing of Yeast Cells.Current protocols in molecular biology · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Shanda R BirkelandDepartment of Pathology, University of Michigan DNA Sequencing Core, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
Natsuko Jin
Alev Cagla Ozdemir
Robert H Lyons
Lois S Weisman
Thomas E Wilson

Funding

Regulation of myosin V interaction with cargo-Equipment SupplementR01GM062261 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Lois S Weisman · 2001 to 2026
$5.8M
MOLECULAR BASIS OF ORGANELLE DIVISION AND SEGREGATIONR01GM050403 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WEISMAN, LOIS S · 1994 to 2015
$5.7M
NIGMS NIH HHS R01 GM050403NIGMS NIH HHS R01-GM050403NIGMS NIH HHS R01 GM062261
6 · The paper itself

Abstract

Many novel and important mutations arise in model organisms and human patients that can be difficult or impossible to identify using standard genetic approaches, especially for complex traits. Working with a previously uncharacterized dominant Saccharomyces cerevisiae mutant with impaired vacuole inheritance, we developed a pooled linkage strategy based on next-generation DNA sequencing to specifically identify functional mutations from among a large excess of polymorphisms, incidental mutations, and sequencing errors. The VAC6-1 mutation was verified to correspond to PHO81-R701S, the highest priority candidate reported by VAMP, the new software platform developed for these studies. Sequence data further revealed the large extent of strain background polymorphisms and structural alterations present in the host strain, which occurred by several mechanisms including a novel Ty insertion. The results provide a snapshot of the ongoing genomic changes that ultimately result in strain divergence and evolution, as well as a general model for the discovery of functional mutations in many organisms.

Indexed as

Genetic LinkageMutationBiological EvolutionDNA Mutational AnalysisGenetic SpeciationGenome, FungalSaccharomyces cerevisiaeSequence Analysis, DNASoftware

Identifiers

PMID20923977
PMCPMC2998298

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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.