Evidence map›Paper›PMID 26102527›Full record

ArticleeLife2015

A panel of induced pluripotent stem cells from chimpanzees: a resource for comparative functional genomics.

Irene Gallego Romero, Bryan J Pavlovic, Irene Hernando-Herraez, Xiang Zhou, Michelle C Ward, Nicholas E Banovich, Courtney L Kagan, Jonathan E Burnett, Constance H Huang, Amy Mitrano and 10 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

89 citing papers in PubMed, 216 citations in OpenAlex.

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29 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

20 authors at 5 institutions in 2 countries.

Irene Gallego RomeroDepartment of Human Genetics, University of Chicago, Chicago, United States.ORCID http://orcid.org/0000-0003-1613-8998
Bryan J PavlovicDepartment of Human Genetics, University of Chicago, Chicago, United States.
Irene Hernando-HerraezParc Recerca Biomèdica de Barcelona, Barcelona, Spain.
Xiang ZhouDepartment of Biostatistics, University of Michigan, Ann Arbor, United States.
Michelle C WardDepartment of Human Genetics, University of Chicago, Chicago, United States.
Nicholas E BanovichDepartment of Human Genetics, University of Chicago, Chicago, United States.
Courtney L KaganDepartment of Human Genetics, University of Chicago, Chicago, United States.
Jonathan E BurnettDepartment of Human Genetics, University of Chicago, Chicago, United States.
Constance H HuangDepartment of Human Genetics, University of Chicago, Chicago, United States.
Amy MitranoDepartment of Human Genetics, University of Chicago, Chicago, United States.
Claudia I ChavarriaDepartment of Human Genetics, University of Chicago, Chicago, United States.
Inbar Friedrich Ben-NunCenter for Regenerative Medicine, Department of Chemical Physiology, The Scripps Research Institute, La Jolla, United States.
Yingchun LiDepartment of Pathology, University of California San Diego, San Diego, United States.
Karen SabatiniCenter for Regenerative Medicine, Department of Chemical Physiology, The Scripps Research Institute, La Jolla, United States.
Trevor R LeonardoCenter for Regenerative Medicine, Department of Chemical Physiology, The Scripps Research Institute, La Jolla, United States.
Mana ParastDepartment of Pathology, University of California San Diego, San Diego, United States.
Tomas Marques-BonetParc Recerca Biomèdica de Barcelona, Barcelona, Spain.
Louise C LaurentSanford Consortium for Regenerative Medicine, La Jolla, United States.
Jeanne F LoringCenter for Regenerative Medicine, Department of Chemical Physiology, The Scripps Research Institute, La Jolla, United States.
Yoav GiladDepartment of Human Genetics, University of Chicago, Chicago, United States.
University of Chicago · USScripps Research Institute · USUniversity of California San Diego · USInstitut de Biologia Evolutiva · ESUniversity of Michigan · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
PREDOCTORAL TRAINING IN GENETICS AND REGULATIONT32GM007197 · NIGMS · UNIVERSITY OF CHICAGO · PI ROTHMAN-DENES, LUCIA B. B · 1985 to 2020
$17.0M
UC San Diego Womens Reproductive Health Research ProgramK12HD001259 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CYNTHIA GYAMFI-BANNERMAN · 1999 to 2026
$9.1M
Natural Selection on Gene Regulation in HumansR01GM077959 · NIGMS · UNIVERSITY OF CHICAGO · PI GILAD, YOAV · 2006 to 2014
$2.9M
Training in Emerging Multidisciplinary Approaches to Mental Health and DiseaseT32MH020065 · NIMH · UNIVERSITY OF CHICAGO · PI NICOLAE, DAN LIVIU, RZHETSKY, ANDREY · 2002 to 2017
$2.3M
Genetic Factors Governing Inter-individual Variation to Oxidative Stress ResponseF31AG044948 · NIA · UNIVERSITY OF CHICAGO · PI BANOVICH, NICHOLAS ELI · 2013 to 2016
$119k
European Research Council 260372NCATS NIH HHS L30 TR001250NIA NIH HHS F31 AG044948NICHD NIH HHS K12 HD001259NIGMS NIH HHS GM007197NIGMS NIH HHS R01 GM077959NIGMS NIH HHS T32 GM007197NIH HHS P51 OD011132NIMH NIH HHS T32 MH020065Wellcome Trust
6 · The paper itself

Abstract

Comparative genomics studies in primates are restricted due to our limited access to samples. In order to gain better insight into the genetic processes that underlie variation in complex phenotypes in primates, we must have access to faithful model systems for a wide range of cell types. To facilitate this, we generated a panel of 7 fully characterized chimpanzee induced pluripotent stem cell (iPSC) lines derived from healthy donors. To demonstrate the utility of comparative iPSC panels, we collected RNA-sequencing and DNA methylation data from the chimpanzee iPSCs and the corresponding fibroblast lines, as well as from 7 human iPSCs and their source lines, which encompass multiple populations and cell types. We observe much less within-species variation in iPSCs than in somatic cells, indicating the reprogramming process erases many inter-individual differences. The low within-species regulatory variation in iPSCs allowed us to identify many novel inter-species regulatory differences of small magnitude.

Indexed as

Cell DifferentiationInduced Pluripotent Stem CellsPan troglodytesAnimalsGene Expression ProfilingGene Expression Regulation, DevelopmentalGenomicsHumansMolecular Sequence DataSequence Analysis, DNAcell panelchimpanzeedevelopmental biologyevolutionary biologygenomicshumaninduced pluripotent stem cellsiPSCPan troglodytesstem cells

Identifiers

PMID26102527
PMCPMC4502404
OpenAlexW2137283360

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.