Evidence map›Paper›PMID 15851675›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

Prospects for identifying functional variation across the genome.

Stuart J Macdonald, Anthony D Long

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. The Neutral Theory in Light of Natural Selection.Molecular biology and evolution · 2018
    Article
  4. Functional classification of 15 million SNPs detected from diverse chicken populations.DNA research : an international journal for rapid publication of reports on genes and genomes · 2015
    Article
  5. Article
  6. Article
  7. Article
  8. Systematics and the origin of species: an introduction.Proceedings of the National Academy of Sciences of the United States of America · 2005
    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 at 1 institution in 1 country.

Stuart J MacdonaldDepartment of Ecology and Evolutionary Biology, University of California, Irvine, 92697-2525, USA. sjm@uci.edu
Anthony D Long
University of California, Irvine · US

Funding

USING DISEQUILIBRIUM MAPPING TO DISSECT COMPLEX TRAITSR01GM058564 · NIGMS · UNIVERSITY OF CALIFORNIA IRVINE · PI LONG, ANTHONY DOUGLAS · 1999 to 2003
$536k
NIGMS NIH HHS GM58564NIGMS NIH HHS R01 GM058564
6 · The paper itself

Abstract

The genetic factors contributing to complex trait variation may reside in regulatory, rather than protein-coding portions of the genome. Within noncoding regions, SNPs in regulatory elements are more likely to contribute to phenotypic variation than those in nonregulatory regions. Thus, it is important to be able to identify and annotate noncoding regulatory elements. DNA conservation among diverged species successfully identifies noncoding regulatory regions. However, because rapidly evolving regulatory regions will not generally be conserved across species, these will not detected by using purely conservation-based methods. Here we describe additional approaches that can be used to identify putative regulatory elements via signatures of nonneutral evolution. An examination of the pattern of polymorphism both within and between populations of Drosophila melanogaster, as well as divergence with its sibling species Drosophila simulans, across 24.2 kb of noncoding DNA identifies several nonneutrally evolving regions not identified by conservation. Because different methods tag different regions, it appears that the methods are complementary. Patterns of variation at different elements are consistent with the action of selective sweeps, balancing selection, or population differentiation. Together with regions conserved between D. melanogaster and Drosophila pseudoobscura, we tag 5.3 kb of noncoding DNA as potentially regulatory. Ninety-seven of the 408 common noncoding SNPs surveyed are within putatively regulatory regions. If these methods collectively identify the majority of functional noncoding polymorphisms, genotyping only these SNPs in an association mapping framework would reduce genotyping effort for noncoding regions 4-fold.

Indexed as

GenomeAnimalsComputational BiologyConserved SequenceDNADrosophilaDrosophila ProteinsEvolution, MolecularGenetic VariationMolecular Sequence DataPolymorphism, GeneticSelection, GeneticDNADrosophila Proteins

Identifiers

PMID15851675
PMCPMC1131871
OpenAlexW2051127190

What OpenQuestion holds

Textmetadata
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.