Evidence map›Paper›PMID 20691772›Full record

ArticleGene2010

Detecting novel genes with sparse arrays.

Mikko Arvas, Niina Haiminen, Bart Smit, Jari Rautio, Marika Vitikainen, Marilyn Wiebe, Diego Martinez, Christine Chee, Joe Kunkel, Charles Sanchez and 5 more

Abstract read
In one paragraph

Article in Gene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Multi-scale genetic dynamic modelling I : an algorithm to compute generators.Theory in biosciences = Theorie in den Biowissenschaften · 2011
    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

15 authors at 5 institutions in 3 countries.

Mikko ArvasVTT Technical Research Centre of Finland, Tietotie 2, PO Box FI-1000, 02044 VTT, Espoo, Finland. mikko.arvas@vtt.fi
Niina Haiminen
Bart Smit
Jari Rautio
Marika Vitikainen
Marilyn Wiebe
Diego Martinez
Christine Chee
Joe Kunkel
Charles Sanchez
Mary Anne Nelson
Tiina Pakula
Markku Saloheimo
Merja Penttilä
Teemu Kivioja
University of New Mexico · USTieto (Finland) · FIUniversity of Helsinki · FIVTT Technical Research Centre of Finland · FIFrieslandCampina (Netherlands) · NL

Funding

UNM Initiative to Maximize Student Diversity (IMSD)R25GM060201 · NIGMS · UNIVERSITY OF NEW MEXICO · PI WERNER-WASHBURNE, MARGRET C. · 2000 to 2017
$9.9M
University of New Mexico: MARC U*STAR Undergraduate Training ProgramT34GM008751 · NIGMS · UNIVERSITY OF NEW MEXICO · PI TAKACS-VESBACH, CRISTINA D. · 2000 to 2021
$6.0M
NIGMS NIH HHS GM060201NIGMS NIH HHS R25 GM060201NIGMS NIH HHS T34GM00851NIGMS NIH HHS T34 GM008751
6 · The paper itself

Abstract

Species-specific genes play an important role in defining the phenotype of an organism. However, current gene prediction methods can only efficiently find genes that share features such as sequence similarity or general sequence characteristics with previously known genes. Novel sequencing methods and tiling arrays can be used to find genes without prior information and they have demonstrated that novel genes can still be found from extensively studied model organisms. Unfortunately, these methods are expensive and thus are not easily applicable, e.g., to finding genes that are expressed only in very specific conditions. We demonstrate a method for finding novel genes with sparse arrays, applying it on the 33.9 Mb genome of the filamentous fungus Trichoderma reesei. Our computational method does not require normalisations between arrays and it takes into account the multiple-testing problem typical for analysis of microarray data. In contrast to tiling arrays, that use overlapping probes, only one 25 mer microarray oligonucleotide probe was used for every 100b. Thus, only relatively little space on a microarray slide was required to cover the intergenic regions of a genome. The analysis was done as a by-product of a conventional microarray experiment with no additional costs. We found at least 23 good candidates for novel transcripts that could code for proteins and all of which were expressed at high levels. Candidate genes were found to neighbour ire1 and cre1 and many other regulatory genes. Our simple, low-cost method can easily be applied to finding novel species-specific genes without prior knowledge of their sequence properties.

Indexed as

Genes, FungalComputational BiologyGene ExpressionGene Expression RegulationGenome, FungalOligonucleotide Array Sequence AnalysisRNA, MessengerSpecies SpecificityTrichodermaRNA, Messenger

Identifiers

PMID20691772
PMCPMC4175568
OpenAlexW2014514099

What OpenQuestion holds

Textmetadata
LicenceTDM
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.