Evidence map›Paper›PMID 17200807›Full record

ArticleJournal of molecular evolution2007

Using variable rate models to identify genes under selection in sequence pairs: their validity and limitations for EST sequences.

Sheri A Church, Kevin Livingstone, Zhao Lai, Alexander Kozik, Steven J Knapp, Richard W Michelmore, Loren H Rieseberg

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Article in Journal of molecular evolution, 2007. 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
–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

1 citing paper in PubMed.

  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

7 authors.

Sheri A ChurchDepartment of Biology, Indiana University, Bloomington, IN 47405, USA. schurch@gwu.edu
Kevin Livingstone
Zhao Lai
Alexander Kozik
Steven J Knapp
Richard W Michelmore
Loren H Rieseberg

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using likelihood-based variable selection models, we determined if positive selection was acting on 523 EST sequence pairs from two lineages of sunflower and lettuce. Variable rate models are generally not used for comparisons of sequence pairs due to the limited information and the inaccuracy of estimates of specific substitution rates. However, previous studies have shown that the likelihood ratio test (LRT) is reliable for detecting positive selection, even with low numbers of sequences. These analyses identified 56 genes that show a signature of selection, of which 75% were not identified by simpler models that average selection across codons. Subsequent mapping studies in sunflower show four of five of the positively selected genes identified by these methods mapped to domestication QTLs. We discuss the validity and limitations of using variable rate models for comparisons of sequence pairs, as well as the limitations of using ESTs for identification of positively selected genes.

Indexed as

Expressed Sequence TagsBase PairingBase SequenceCodonDNA, PlantEvolution, MolecularGenome, PlantHelianthusLactucaLikelihood FunctionsReproducibility of ResultsSelection, GeneticCodonDNA, Plant

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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.