Evidence map›Paper›PMID 30446528›Full record

ArticleGenome research2018

Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of

Chun Jimmie Ye, Jenny Chen, Alexandra-Chloé Villani, Rachel E Gate, Meena Subramaniam, Tushar Bhangale, Mark N Lee, Towfique Raj, Raktima Raychowdhury, Weibo Li and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

  1. Pooled it
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  15. Association ofFrontiers in immunology · 2024
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  19. Archaic hominin traits through the splicing lens.Nature ecology & evolution · 2023
    Article
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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

22 authors at 5 institutions in 1 country.

Chun Jimmie Ye *Institute for Human Genetics, Institute for Health and Computational Sciences, Department of Biostatistics and Epidemiology, Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, California 94143, USA.
Jenny Chen *Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Alexandra-Chloé VillaniBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Rachel E GateInstitute for Human Genetics, Institute for Health and Computational Sciences, Department of Biostatistics and Epidemiology, Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, California 94143, USA.
Meena SubramaniamInstitute for Human Genetics, Institute for Health and Computational Sciences, Department of Biostatistics and Epidemiology, Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, California 94143, USA.
Tushar BhangaleGenentech Incorporated, South San Francisco, California 94080, USA.
Mark N LeeBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Towfique RajBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Raktima RaychowdhuryBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Weibo LiBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Noga RogelBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Sean SimmonsBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Selina H ImboywaHarvard Medical School, Boston, Massachusetts 02116, USA.
Portia I ChipendoHarvard Medical School, Boston, Massachusetts 02116, USA.
Cristin McCabeBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Michelle H LeeHarvard Medical School, Boston, Massachusetts 02116, USA.
Irene Y FrohlichHarvard Medical School, Boston, Massachusetts 02116, USA.
Barbara E StrangerSection of Genetic Medicine, Department of Medicine, Institute for Genomics and Systems Biology, Center for Data Intensive Science, The University of Chicago, Chicago, Illinois 60637, USA.
Philip L De JagerBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Aviv RegevBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Tim BehrensGenentech Incorporated, South San Francisco, California 94080, USA.
Nir HacohenBroad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Broad Institute · USHarvard University · USQB3 · USSunesis (United States) · USUniversity of Chicago · US

Funding

Center for Cell CircuitsP50HG006193 · NHGRI · BROAD INSTITUTE, INC. · PI REGEV, AVIV · 2011 to 2015
$15.6M
Center for Cell CircuitsRM1HG006193 · NHGRI · BROAD INSTITUTE, INC. · PI BLAINEY, PAUL CLARK, HACOHEN, NIR · 2016 to 2020
$14.9M
Gene Expression and Regulatory Networks in Human LeukocytesRC2GM093080 · NIGMS · HARVARD MEDICAL SCHOOL · PI BENOIST, CHRISTOPHE O., MATHIS, DIANE J · 2009 to 2010
$7.3M
BMI Bioinformatics Training GrantsT32GM067547 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HERNANDEZ, RYAN D. · 2003 to 2022
$6.6M
Genetic regulation and immunological function of ERAP2 haplotypesR01AI136972 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI YE, CHUN JIMMIE · 2018 to 2022
$3.5M
Cancer Immunology Training GrantT32CA207021 · NCI · DANA-FARBER CANCER INST · PI WUCHERPFENNIG, KAI W · 2016 to 2020
$2.4M
Fine mapping rheumatic disease variants using functional genomic sequencingR01AR071522 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI YE, CHUN JIMMIE · 2017 to 2020
$1.5M
NCI NIH HHS T32 CA207021NHGRI NIH HHS P50 HG006193NHGRI NIH HHS RM1 HG006193NIAID NIH HHS R01 AI136972NIAMS NIH HHS R01 AR071522NIGMS NIH HHS RC2 GM093080
6 · The paper itself

Abstract

While genetic variants are known to be associated with overall gene abundance in stimulated immune cells, less is known about their effects on alternative isoform usage. By analyzing RNA-seq profiles of monocyte-derived dendritic cells from 243 individuals, we uncovered thousands of unannotated isoforms synthesized in response to influenza infection and type 1 interferon stimulation. We identified more than a thousand quantitative trait loci (QTLs) associated with alternate isoform usage (isoQTLs), many of which are independent of expression QTLs (eQTLs) for the same gene. Compared with eQTLs, isoQTLs are enriched for splice sites and untranslated regions, but depleted of sequences upstream of annotated transcription start sites. Both eQTLs and isoQTLs explain a significant proportion of the disease heritability attributed to common genetic variants. At the

Indexed as

Alternative SplicingGenetic Predisposition to DiseaseInfluenza A virusAdolescentAdultAminopeptidasesChromosome MappingComputational BiologyDendritic CellsFemaleGene Expression ProfilingGene Expression RegulationGene OntologyGenetic TestingGenetic VariationHost-Pathogen InteractionsAminopeptidasesERAP2 protein, humanInterferon Type I

Identifiers

PMID30446528
PMCPMC6280757
OpenAlexW2950448212

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.