Evidence map›Paper›PMID 16288651›Full record

ArticleBMC genomics2005

Leveraging human genomic information to identify nonhuman primate sequences for expression array development.

Eliot R Spindel, Mark A Pauley, Yibing Jia, Courtney Gravett, Shaun L Thompson, Nicholas F Boyle, Sergio R Ojeda, Robert B Norgren

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  9. Translating the brain transcriptome in neuroAIDS: from non-human primates to humans.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2012
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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

8 authors at 3 institutions in 1 country.

Eliot R SpindelDivision of Neuroscience, Oregon National Primate Research Center, Beaverton, OR 97006, USA. spindele@ohsu.edu
Mark A Pauley
Yibing Jia
Courtney Gravett
Shaun L Thompson
Nicholas F Boyle
Sergio R Ojeda
Robert B Norgren
Oregon National Primate Research Center · USUniversity of Nebraska Medical Center · USUniversity of Nebraska at Omaha · US

Funding

Gene-Targeted SNP discovery in rhesus macaquesR24RR017444 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI NORGREN, ROBERT B. · 2003 to 2011
$5.2M
NCRR NIH HHS R24 RR017444NCRR NIH HHS RR017444
6 · The paper itself

Abstract

backgroundNonhuman primates (NHPs) are essential for biomedical research due to their similarities to humans. The utility of NHPs will be greatly increased by the application of genomics-based approaches such as gene expression profiling. Sequence information from the 3' end of genes is the key resource needed to create oligonucleotide expression arrays.

resultsWe have developed the algorithms and procedures necessary to quickly acquire sequence information from the 3' end of nonhuman primate orthologs of human genes. To accomplish this, we identified terminal exons of over 15,000 human genes by aligning mRNA sequences with genomic sequence. We found the mean length of complete last exons to be approximately 1,400 bp, significantly longer than previous estimates. We designed primers to amplify genomic DNA, which included at least 300 bp of the terminal exon. We cloned and sequenced the PCR products representing over 5,500 Macaca mulatta (rhesus monkey) orthologs of human genes. This sequence information has been used to select probes for rhesus gene expression profiling. We have also tested 10 sets of primers with genomic DNA from Macaca fascicularis (Cynomolgus monkey), Papio hamadryas (Baboon), and Chlorocebus aethiops (African green monkey, vervet). The results indicate that the primers developed for this study will be useful for acquiring sequence from the 3' end of genes for other nonhuman primate species.

conclusionThis study demonstrates that human genomic DNA sequence can be leveraged to obtain sequence from the 3' end of NHP orthologs and that this sequence can then be used to generate NHP oligonucleotide microarrays. Affymetrix and Agilent used sequences obtained with this approach in the design of their rhesus macaque oligonucleotide microarrays.

Indexed as

Gene Expression ProfilingGenetic TechniquesGenome, HumanAlgorithmsAnimalsChlorocebus aethiopsCloning, MolecularDNA, ComplementaryDNA PrimersExonsGene ExpressionGenomicsHumansMacaca mulattaModels, GeneticOligonucleotide Array Sequence AnalysisDNA, ComplementaryDNA PrimersOligonucleotidesRNA, Messenger

Identifiers

PMID16288651
PMCPMC1314899
OpenAlexW2112044690

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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.