Evidence map›Paper›PMID 21400220›Full record

ArticleGenetica2011

Detection of selection utilizing molecular phylogenetics: a possible approach.

Ming Yang, Gerald J Wyckoff

Abstract read
In one paragraph

Article in Genetica, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ming YangDivision of Molecular Biology and Biochemistry, University of Missouri-Kansas City, SCB Room 518, 5007 Rockhill Rd., Kansas City, MO 64110, USA.
Gerald J Wyckoff

Funding

Role of ZIC and GLI Protein-protein Interactions in Human Brain DisordersR15HD055668 · NICHD · UNIVERSITY OF MISSOURI KANSAS CITY · PI WYCKOFF, GERALD J · 2008 to 2008
$221k
DEVELOPMENT OF CHEMINFORMATIC MODULE FOR INFORMATION CONTENT ANALYSIS SOFTWARER41GM088922 · NIGMS · BIOINFORMATICA, LLC · PI WYCKOFF, GERALD J · 2010 to 2010
$128k
NICHD NIH HHS 1R15HD055668-01A1NICHD NIH HHS R15 HD055668NIGMS NIH HHS 1R41GM088922-01A1NIGMS NIH HHS R41 GM088922
6 · The paper itself

Abstract

The neutral theory of molecular evolution (Kimura 1985) is the basis for most current statistical tests for detecting selection, mainly using polymorphism data within species, divergence data between species, and/or genomic structures like linkage disequilibrium (Wang et al. 2006). In most cases informative tests can only be constructed with ample variations within these parameters and many common tests are difficult to formulate when identity-by-descent is not clear, for example in gene families or repetitive elements. With the current progress being made toward whole-genome sequencing and re-sequencing efforts, as well as protein sequencing via tandem mass spectrometry where genomic sequencing is lacking, we felt it was necessary to re-visit possible methods for rapid screening and detection of evolutionary outliers. These outliers might be of interest for other research, such as candidate gene association studies or genome annotations, drug- and disease-target searches, and functional studies. We focused on methods that would work on both protein and nucleotide data, could be used on large gene or protein domain families, and could be generated quickly in order for "first pass" annotation of large scale data. For these reasons, we chose properties of trees generated routinely in molecular phylogenetic studies; genetic distance, tree shape and balance, and internal node statistics (Heard 1992). Our current research looking at protein domain family data and phylogenetic trees from PFAM (Finn et al. 2008) suggests this approach towards detecting evolutionary outliers is feasible, but additional work will be necessary to determine the parameters that suggest either positive or negative selection is occurring in specific gene families. This is particularly true when other factors such as rapid duplication and deletion of genes containing these domains is taking place, and we suggest phylogenetic statistics may be useful in combination with existing methodologies for detailed studies of gene family data.

Indexed as

Evolution, MolecularPhylogenyComputational BiologyGenomeProteinsProteins

Identifiers

PMID21400220
PMCPMC3980844

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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.