Evidence map›Paper›PMID 8076940›Full record

ArticleHuman genetics1994

Population genetic characteristics of the D1S80 locus in seven human populations.

R Deka, S DeCroo, L Jin, S T McGarvey, F Rothhammer, R E Ferrell, R Chakraborty

Abstract read
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In one paragraph

Article in Human genetics, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 50 citations in OpenAlex.

  1. Mutation at the human D1S80 minisatellite locus.TheScientificWorldJournal · 2012
    Article
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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 at 4 institutions in 2 countries.

R DekaDepartment of Human Genetics, University of Pittsburgh, PA 15261.
S DeCroo
L Jin
S T McGarvey
F Rothhammer
R E Ferrell
R Chakraborty
University of Pittsburgh · USThe University of Texas Health Science Center at Houston · USMiriam Hospital · USUniversity of Chile · CL

Funding

POPULATION MIXTURES EFFECTS ON GENETIC VARIATIONR01GM041399 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHAKRABORTY, RANAJIT · 1990 to 2007
$1.3M
POPULATION GENETICS OF HYPERVARIABLE LOCIR01GM045861 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEKA, RANJAN · 1992 to 2000
$191k
ADIPOSITY INSULIN ELECTROLYTES AND SAMOAN BLOOD PRESSURER01AG009375 · NIA · MIRIAM HOSPITAL · PI MCGARVEY, STEPHEN T. · 1990 to 1994
–
NIA NIH HHS AG 09375NIGMS NIH HHS GM 41399NIGMS NIH HHS GM 45861
6 · The paper itself

Abstract

We have analyzed the allele frequency distribution at the highly polymorphic variable number of tandem repeat (VNTR) locus D1S80 (pMCT118) in seven ethnic populations (namely, New Guinea Highlanders of Papua New Guinea, Dogrib Indians of Canada, Pehuenche Indians of Chile, American and Western Samoans, Kacharis of Northeast India, and German Caucasians) using the polymerase chain reaction (PCR) technique. In the pooled sample of 443 unrelated individuals 20 segregating alleles were detected. A trimodal pattern of allelic distribution is present in the majority of populations and is indicative of the evolutionary antiquity of the polymorphism at this locus. In spite of the observed high degree of polymorphism (expected heterozygosity 56%-86%), with a single exception--the marginally significant P value (0.04) of the exact test in American Samoans--the genotype distributions in all populations conform to their respective Hardy-Weinberg expectations. Summary statistics indicate that, in general, the allele frequency distribution at this locus may be approximated by the infinite allele model. The data also demonstrate that alleles that are shared by all populations have the highest average frequency within populations. Furthermore, the kinship bioassay analysis demonstrates that the extensive variation observed at the D1S80 locus is at the interindividual within population level, which dwarfs any interpopulation allele frequency variation, consistent with the population dynamics of hypervariable polymorphisms. These characteristics of the D1S80 locus make it a very useful marker for population genetic research, genetic linkage studies, forensic identification of individuals, and for determination of biological relatedness of individuals.

Indexed as

AllelesGene FrequencyPolymorphism, GeneticRepetitive Sequences, Nucleic AcidBase SequenceBiological EvolutionDNAElectrophoresis, Agar GelEthnicityHumansMolecular Sequence DataMutationPolymerase Chain ReactionDNA

Identifiers

PMID8076940
OpenAlexW2080726106

What OpenQuestion holds

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Registered trials

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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.