Evidence map›Paper›PMID 23729657›Full record

ArticleDatabase : the journal of biological databases and curation2013

The non-obese diabetic mouse sequence, annotation and variation resource: an aid for investigating type 1 diabetes.

Charles A Steward, Jose M Gonzalez, Steve Trevanion, Dan Sheppard, Giselle Kerry, James G R Gilbert, Linda S Wicker, Jane Rogers, Jennifer L Harrow

Open access · goldAbstract read
In one paragraph

Article in Database : the journal of biological databases and curation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Mouse Models of Autoimmune Diabetes: The Nonobese Diabetic (NOD) Mouse.Methods in molecular biology (Clifton, N.J.) · 2020
    Article
  7. Article
  8. Review
  9. Article
  10. Creating reference gene annotation for the mouse C57BL6/J genome assembly.Mammalian genome : official journal of the International Mammalian Genome Society · 2015
    Article
  11. The Mouse Genomes Project: a repository of inbred laboratory mouse strain genomes.Mammalian genome : official journal of the International Mammalian Genome Society · 2015
    Article
  12. 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

9 authors at 4 institutions in 1 country.

Charles A StewardThe Wellcome Trust Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK. cas@sanger.ac.uk
Jose M Gonzalez
Steve Trevanion
Dan Sheppard
Giselle Kerry
James G R Gilbert
Linda S Wicker
Jane Rogers
Jennifer L Harrow
Earlham Institute · GBWellcome Sanger Institute · GBUniversity of Cambridge · GBNorwich Research Park · GB

Funding

NIAID NIH HHS AI 15416Wellcome Trust 091157Wellcome Trust 096388Wellcome Trust 100140
6 · The paper itself

Abstract

Model organisms are becoming increasingly important for the study of complex diseases such as type 1 diabetes (T1D). The non-obese diabetic (NOD) mouse is an experimental model for T1D having been bred to develop the disease spontaneously in a process that is similar to humans. Genetic analysis of the NOD mouse has identified around 50 disease loci, which have the nomenclature Idd for insulin-dependent diabetes, distributed across at least 11 different chromosomes. In total, 21 Idd regions across 6 chromosomes, that are major contributors to T1D susceptibility or resistance, were selected for finished sequencing and annotation at the Wellcome Trust Sanger Institute. Here we describe the generation of 40.4 mega base-pairs of finished sequence from 289 bacterial artificial chromosomes for the NOD mouse. Manual annotation has identified 738 genes in the diabetes sensitive NOD mouse and 765 genes in homologous regions of the diabetes resistant C57BL/6J reference mouse across 19 candidate Idd regions. This has allowed us to call variation consequences between homologous exonic sequences for all annotated regions in the two mouse strains. We demonstrate the importance of this resource further by illustrating the technical difficulties that regions of inter-strain structural variation between the NOD mouse and the C57BL/6J reference mouse can cause for current next generation sequencing and assembly techniques. Furthermore, we have established that the variation rate in the Idd regions is 2.3 times higher than the mean found for the whole genome assembly for the NOD/ShiLtJ genome, which we suggest reflects the fact that positive selection for functional variation in immune genes is beneficial in regard to host defence. In summary, we provide an important resource, which aids the analysis of potential causative genes involved in T1D susceptibility. Database URLs: http://www.sanger.ac.uk/resources/mouse/nod/; http://vega-previous.sanger.ac.uk/info/data/mouse_regions.html#Idd

Indexed as

Genetic VariationMolecular Sequence AnnotationAnimalsBase PairingBase SequenceDiabetes Mellitus, Type 1Genetic LociGenomeHumansMiceMice, Inbred C57BLMice, Inbred NODPolymorphism, Single NucleotideSequence AlignmentSequence Analysis, DNA

Identifiers

PMID23729657
PMCPMC3668384
OpenAlexW2168786749

What OpenQuestion holds

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LicenceCC BY-NC
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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.