Evidence map›Paper›PMID 25572914›Full record

ArticleBMC genomics2014

Robustness of birth-death and gain models for inferring evolutionary events.

Maureen Stolzer, Larry Wasserman, Dannie Durand

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 39% of its field
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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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

3 authors at 1 institution in 1 country.

Maureen Stolzer
Larry Wasserman
Dannie Durand
Carnegie Mellon University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhylogenetic birth-death models are opening a new window on the processes of genome evolution in studies of the evolution of gene and protein families, protein-protein interaction networks, microRNAs, and copy number variation. Given a species tree and a set of genomic characters in present-day species, the birth-death approach estimates the most likely rates required to explain the observed data and returns the expected ancestral character states and the history of character state changes. Achieving a balance between model complexity and generalizability is a fundamental challenge in the application of birth-death models. While more parameters promise greater accuracy and more biologically realistic models, increasing model complexity can lead to overfitting and a heavy computational cost.

resultsHere we present a systematic, empirical investigation of these tradeoffs, using protein domain families in six metazoan genomes as a case study. We compared models of increasing complexity, implemented in the Count program, with respect to model fit, robustness, and stability. In addition, we used a bootstrapping procedure to assess estimator variability. The results show that the most complex model, which allows for both branch-specific and family-specific rate variation, achieves the best fit, without overfitting. Variance remains low with increasing complexity, except for family-specific loss rates. This variance is reduced when the number of discrete rate categories is increased.

conclusionsThe work presented here evaluates model choice for genomic birth-death models in a systematic way and presents the first use of bootstrapping to assess estimator variance in birth-death models. We find that a model incorporating both lineage and family rate variation yields more accurate estimators without sacrificing generality. Our results indicate that model choice can lead to fundamentally different evolutionary conclusions, emphasizing the importance of more biologically realistic and complex models.

Indexed as

Evolution, MolecularGenomeModels, GeneticPhylogenyGenomics

Identifiers

PMID25572914
PMCPMC4239551
OpenAlexW2130824474

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.