Evidence map›Paper›PMID 18215302›Full record

ArticleBMC evolutionary biology2008

A genome-wide screen for noncoding elements important in primate evolution.

Eliot C Bush, Bruce T Lahn

Abstract read
In one paragraph

Article in BMC evolutionary biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 2 pooled it
–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

59 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Modular genetic architecture underlies human hand and foot evolution.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  15. The genetic architecture of the human skeletal form.bioRxiv : the preprint server for biology · 2023
    Article
  16. The evolutionary origin of psychosis.Frontiers in psychiatry · 2023
    Article
  17. Review
  18. Using neuroimaging genomics to investigate the evolution of human brain structure.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Article
  20. 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

2 authors.

Eliot C BushDepartment of Human Genetics and Howard Hughes Medical Institute, University of Chicago, Chicago, Illinois, USA. bush@hmc.edu
Bruce T Lahn

Funding

NHLBI NIH HHS HL07605
6 · The paper itself

Abstract

backgroundA major goal in the study of human evolution is to identify key genetic changes which occurred over the course of primate evolution. According to one school of thought, many such changes are likely to be found in noncoding sequence. An approach to identifying these involves comparing multiple genomes to identify conserved regions with an accelerated substitution rate in a particular lineage. Such acceleration could be the result of positive selection.

resultsHere we develop a likelihood ratio test method to identify such regions. We apply it not only to the human terminal lineage, as has been done in previous studies, but also to a number of other branches in the primate tree. We present the top scoring elements, and compare our results with previous studies. We also present resequencing data from one particular element accelerated on the human lineage. These data indicate that the element lies in a region of low polymorphism in humans, consistent with the possibility of a recent selective sweep. They also show that the AT to GC bias for polymorphism in this region differs dramatically from that for substitutions.

conclusionOur results suggest that screens of this type will be helpful in unraveling the complex set of changes which occurred during primate evolution.

Indexed as

GenomeAnimalsBase SequenceConserved SequenceEvolution, MolecularGenome, HumanHumansLikelihood FunctionsPhylogenyPolymorphism, Single NucleotidePrimatesSelection, GeneticSequence Analysis, DNA

Identifiers

PMID18215302
PMCPMC2242780

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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.