Evidence map›Paper›PMID 24714809›Full record

ArticleGenome research2014

Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines.

Wen Huang, Andreas Massouras, Yutaka Inoue, Jason Peiffer, Miquel Ràmia, Aaron M Tarone, Lavanya Turlapati, Thomas Zichner, Dianhui Zhu, Richard F Lyman and 41 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 405 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
405citing papers in PubMed, 1 pooled it
–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

405 citing papers in PubMed, 1 synthesis or guideline pooled it, 698 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Regulatory logic of neuronal differentiation in theProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Article
  8. Female genetic variation controlling timing of mating plug ejection inbioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Methylation-associated mutagenesis underlies variation in the mutation spectrum across eukaryotes.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  14. Article
  15. RNA-binding is the essential biological function of thebioRxiv : the preprint server for biology · 2026
    Article
  16. Article
  17. Article
  18. Inferring the genetic basis of sleep states inbioRxiv : the preprint server for biology · 2026
    Article
  19. Review
  20. Article

345 more citing papers are in PubMed but not listed here.

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

51 authors at 8 institutions in 5 countries.

Wen HuangDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Andreas MassourasLaboratory of Systems Biology and Genetics, Institute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland; Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland;
Yutaka InoueCenter for Education in Liberal Arts and Sciences, Osaka University, Osaka-fu, 560-0043 Japan;
Jason PeifferDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Miquel RàmiaGenomics, Bioinformatics and Evolution Group, Institut de Biotecnologia i de Biomedicina (IBB), Department of Genetics and Microbiology, Campus Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain;
Aaron M TaroneDepartment of Entomology, Texas A&M University, College Station, Texas 77843, USA;
Lavanya TurlapatiDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Thomas ZichnerGenome Biology Unit, European Molecular Biology Laboratory (EMBL), 69117 Heidelberg, Germany;
Dianhui ZhuHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Richard F LymanDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Michael M MagwireDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Kerstin BlankenburgHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Mary Anna CarboneDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Kyle ChangHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Lisa L EllisDepartment of Entomology, Texas A&M University, College Station, Texas 77843, USA;
Sonia FernandezHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Yi HanHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Gareth HighnamVirginia Tech Virginia Bioinformatics Institute and Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia 24061, USA.
Carl E HjelmenDepartment of Entomology, Texas A&M University, College Station, Texas 77843, USA;
John R JackDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Mehwish JavaidHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Joy JayaseelanHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Divya KalraHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Sandy LeeHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Lora LewisHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Mala MunidasaHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Fiona OngeriHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Shohba PatelHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Lora PeralesHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Agapito PerezHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
LingLing PuHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Stephanie M RollmannDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Robert RuthHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Nehad SaadaHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Crystal WarnerHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Aneisa WilliamsHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Yuan-Qing WuHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Akihiko YamamotoDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Yiqing ZhangHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Yiming ZhuHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Robert R H AnholtDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Jan O KorbelGenome Biology Unit, European Molecular Biology Laboratory (EMBL), 69117 Heidelberg, Germany;
David MittelmanVirginia Tech Virginia Bioinformatics Institute and Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia 24061, USA.
Donna M MuznyHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Richard A GibbsHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Antonio BarbadillaGenomics, Bioinformatics and Evolution Group, Institut de Biotecnologia i de Biomedicina (IBB), Department of Genetics and Microbiology, Campus Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain;
J Spencer JohnstonDepartment of Entomology, Texas A&M University, College Station, Texas 77843, USA;
Eric A StoneDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Stephen RichardsHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030 USA;
Bart DeplanckeLaboratory of Systems Biology and Genetics, Institute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland; Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland;
Trudy F C MackayDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27595, USA;
Baylor College of Medicine · USNorth Carolina State University · USTexas A&M University · USEuropean Molecular Biology Laboratory · DESIB Swiss Institute of Bioinformatics · CHUniversitat Autònoma de Barcelona · ESVirginia Tech · USOsaka University of Arts · JP

Funding

The Human Genome Sequencing CenterU54HG003273 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2004 to 2015
$341.3M
Molecular Genetics of Olfaction in DrosophiliaR01GM059469 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI ANHOLT, ROBERT R. H, MACKAY, TRUDY F. · 1999 to 2016
$5.8M
QUANTITATIVE TRAIT LOCI IN DROSOPHILAR01GM045146 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI ANHOLT, ROBERT R. H, MACKAY, TRUDY F. · 1991 to 2012
$5.1M
Genetics of Alcohol Sensitivity in DrosophilaR01AA016560 · NIAAA · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI ANHOLT, ROBERT R. H, MACKAY, TRUDY F. · 2007 to 2016
$4.0M
Genetics of Aggression in DrosophilaR01GM076083 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI ANHOLT, ROBERT R. H, MACKAY, TRUDY F. · 2006 to 2015
$2.4M
NHGRI NIH HHS U54 HG003273NIAAA NIH HHS R01 AA016560NIGMS NIH HHS R01 GM045146NIGMS NIH HHS R01 GM059469NIGMS NIH HHS R01 GM076083NIGMS NIH HHS R01GM076083NIGMS NIH HHS R01 GM45146NIGMS NIH HHS R01 GM 59469
6 · The paper itself

Abstract

The Drosophila melanogaster Genetic Reference Panel (DGRP) is a community resource of 205 sequenced inbred lines, derived to improve our understanding of the effects of naturally occurring genetic variation on molecular and organismal phenotypes. We used an integrated genotyping strategy to identify 4,853,802 single nucleotide polymorphisms (SNPs) and 1,296,080 non-SNP variants. Our molecular population genomic analyses show higher deletion than insertion mutation rates and stronger purifying selection on deletions. Weaker selection on insertions than deletions is consistent with our observed distribution of genome size determined by flow cytometry, which is skewed toward larger genomes. Insertion/deletion and single nucleotide polymorphisms are positively correlated with each other and with local recombination, suggesting that their nonrandom distributions are due to hitchhiking and background selection. Our cytogenetic analysis identified 16 polymorphic inversions in the DGRP. Common inverted and standard karyotypes are genetically divergent and account for most of the variation in relatedness among the DGRP lines. Intriguingly, variation in genome size and many quantitative traits are significantly associated with inversions. Approximately 50% of the DGRP lines are infected with Wolbachia, and four lines have germline insertions of Wolbachia sequences, but effects of Wolbachia infection on quantitative traits are rarely significant. The DGRP complements ongoing efforts to functionally annotate the Drosophila genome. Indeed, 15% of all D. melanogaster genes segregate for potentially damaged proteins in the DGRP, and genome-wide analyses of quantitative traits identify novel candidate genes. The DGRP lines, sequence data, genotypes, quality scores, phenotypes, and analysis and visualization tools are publicly available.

Indexed as

Genetic VariationGenome, InsectPhenotypeAnimalsChromatinDrosophila melanogasterFemaleGenetic LinkageGenome SizeGenome-Wide Association StudyGenotypeGenotyping TechniquesHigh-Throughput Nucleotide SequencingINDEL MutationLinkage DisequilibriumMaleChromatin

Identifiers

PMID24714809
PMCPMC4079974
OpenAlexW2102907886

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.