Evidence map›Paper›PMID 27049301›Full record

ArticleEuropean journal of human genetics : EJHG2016

Whole-exome sequencing in an isolated population from the Dalmatian island of Vis.

Ana Jeroncic, Yasin Memari, Graham Rs Ritchie, Audrey E Hendricks, Anja Kolb-Kokocinski, Angela Matchan, Veronique Vitart, Caroline Hayward, Ivana Kolcic, Dominik Glodzik and 7 more

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Article
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  5. Article
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  8. Review
  9. Clinical Interpretation of Genomic Variations.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2016
    Review
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

17 authors.

Ana JeroncicDepartment of Research in Biomedicine and Health, University of Split School of Medicine, Split, Croatia.
Yasin MemariWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Graham Rs RitchieWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Audrey E HendricksWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Anja Kolb-KokocinskiWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Angela MatchanWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Veronique VitartMRC Human Genetics Unit, Institute for Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Caroline HaywardMRC Human Genetics Unit, Institute for Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Ivana KolcicDepartment of Public Health, University of Split School of Medicine, Split, Croatia.
Dominik GlodzikMRC Human Genetics Unit, Institute for Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Alan F WrightMRC Human Genetics Unit, Institute for Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Igor RudanCentre for Global Health Research, University of Edinburgh, Edinburgh, UK.
Harry CampbellCentre for Global Health Research, University of Edinburgh, Edinburgh, UK.
Richard DurbinWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Ozren PolašekDepartment of Public Health, University of Split School of Medicine, Split, Croatia.
Eleftheria ZegginiWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Vesna Boraska PericaWellcome Trust Sanger Institute, Hinxton, Cambridge, UK.

Funding

Medical Research Council MC_PC_U127561128Wellcome Trust 098051
6 · The paper itself

Abstract

We have whole-exome sequenced 176 individuals from the isolated population of the island of Vis in Croatia in order to describe exonic variation architecture. We found 290 577 single nucleotide variants (SNVs), 65% of which are singletons, low frequency or rare variants. A total of 25 430 (9%) SNVs are novel, previously not catalogued in NHLBI GO Exome Sequencing Project, UK10K-Generation Scotland, 1000Genomes Project, ExAC or NCBI Reference Assembly dbSNP. The majority of these variants (76%) are singletons. Comparable to data obtained from UK10K-Generation Scotland that were sequenced and analysed using the same protocols, we detected an enrichment of potentially damaging variants (non-synonymous and loss-of-function) in the low frequency and common variant categories. On average 115 (range 93-140) genotypes with loss-of-function variants, 23 (15-34) of which were homozygous, were identified per person. The landscape of loss-of-function variants across an exome revealed that variants mainly accumulated in genes on the xenobiotic-related pathways, of which majority coded for enzymes. The frequency of loss-of-function variants was additionally increased in Vis runs of homozygosity regions where variants mainly affected signalling pathways. This work confirms the isolate status of Vis population by means of whole-exome sequence and reveals the pattern of loss-of-function mutations, which resembles the trails of adaptive evolution that were found in other species. By cataloguing the exomic variants and describing the allelic structure of the Vis population, this study will serve as a valuable resource for future genetic studies of human diseases, population genetics and evolution in this population.

Indexed as

ExomeCroatiaEvolution, MolecularGene FrequencyHumansIslandsMutationPolymorphism, Single NucleotidePopulationReproductive Isolation

Identifiers

PMID27049301
PMCPMC4950961

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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.