Evidence map›Paper›PMID 27160605›Full record

ArticleNature communications2016

Predicting quantitative traits from genome and phenome with near perfect accuracy.

Kaspar Märtens, Johan Hallin, Jonas Warringer, Gianni Liti, Leopold Parts

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. High-Throughput, High-Precision Colony Phenotyping with Pyphe.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. Article
  7. Characterization of Cold-TolerantMicroorganisms · 2021
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Artificial Intelligence for Cardiac Imaging-Genetics Research.Frontiers in cardiovascular medicine · 2019
    Review
  15. Article
  16. Article
  17. Patient Similarity Networks for Precision Medicine.Journal of molecular biology · 2018
    Review
  18. Article
  19. Article
  20. Review
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

5 authors.

Kaspar MärtensInstitute of Computer Science, University of Tartu, Tartu 50409, Estonia.
Johan HallinInstitute for Research on Cancer and Aging, University of Sophia Antipolis, Nice 02 06107, France.
Jonas WarringerDepartment of Chemistry and Molecular Biology, Gothenburg University, Gothenburg 40530, Sweden.
Gianni LitiInstitute for Research on Cancer and Aging, University of Sophia Antipolis, Nice 02 06107, France.
Leopold PartsInstitute of Computer Science, University of Tartu, Tartu 50409, Estonia.

Funding

Wellcome Trust
6 · The paper itself

Abstract

In spite of decades of linkage and association studies and its potential impact on human health, reliable prediction of an individual's risk for heritable disease remains difficult. Large numbers of mapped loci do not explain substantial fractions of heritable variation, leaving an open question of whether accurate complex trait predictions can be achieved in practice. Here, we use a genome sequenced population of ∼7,000 yeast strains of high but varying relatedness, and predict growth traits from family information, effects of segregating genetic variants and growth in other environments with an average coefficient of determination R(2) of 0.91. This accuracy exceeds narrow-sense heritability, approaches limits imposed by measurement repeatability and is higher than achieved with a single assay in the laboratory. Our results prove that very accurate prediction of complex traits is possible, and suggest that additional data from families rather than reference cohorts may be more useful for this purpose.

Indexed as

Genome, FungalQuantitative Trait, HeritableDiploidyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansHybridization, GeneticModels, GeneticPhenotypeQuantitative Trait LociSaccharomyces cerevisiae

Identifiers

PMID27160605
PMCPMC4866306

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Registered trials

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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.