Evidence map›Paper›PMID 12600278›Full record

ArticleBMC genomics2003

STRP screening sets for the human genome at 5 cM density.

Nader Ghebranious, David Vaske, Adong Yu, Chengfeng Zhao, Gabor Marth, James L Weber

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 46 citations in OpenAlex.

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  8. A genomic portrait of human microsatellite variation.Molecular biology and evolution · 2011
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  19. Informativeness of genetic markers for inference of ancestry.American journal of human genetics · 2003
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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

6 authors at 3 institutions in 1 country.

Nader GhebraniousMolecular Diagnostic Genotyping Laboratory, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA. ghebranious.nader@marshfieldclinic.org
David Vaske
Adong Yu
Chengfeng Zhao
Gabor Marth
James L Weber
Marshfield Clinic · USNational Institutes of Health · USPioneer Hi-Bred · US

Funding

MAMMALIAN GENOTYPING SERVICEN01HV048141 · HV · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI WEBER, JAMES L. · 1994 to 2000
$3.1M
NHLBI NIH HHS HV48141NHLBI NIH HHS N01 HV048141
6 · The paper itself

Abstract

backgroundShort tandem repeat polymorphisms (STRPs) are powerful tools for gene mapping and other applications. A STRP genome scan of 10 cM is usually adequate for mapping single gene disorders. However mapping studies involving genetically complex disorders and especially association (linkage disequilibrium) often require higher STRP density.

resultsWe report the development of two separate 10 cM human STRP Screening Sets (Sets 12 and 52) which span all chromosomes. When combined, the two Sets contain a total of 782 STRPs, with average STRP spacing of 4.8 cM, average heterozygosity of 0.72, and total sex-average coverage of 3535 cM. The current Sets are comprised almost entirely of STRPs based on tri- and tetranucleotide repeats. We also report correction of primer sequences for many STRPs used in previous Screening Sets. Detailed information for the new Screening Sets is available from our web site: http://research.marshfieldclinic.org/genetics.

conclusionOur new human STRP Screening Sets will improve the quality and cost effectiveness of genotyping for gene mapping and other applications.

Indexed as

Genome, HumanBase SequenceChromosome MappingGenetic TestingHumansMicrosatellite RepeatsMolecular Sequence DataPolymorphism, Genetic

Identifiers

PMID12600278
PMCPMC152641
OpenAlexW2124853778

What OpenQuestion holds

Textmetadata
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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.