Evidence map›Paper›PMID 30778230›Full record

ArticleNature biotechnology2019

Multi-omic measurements of heterogeneity in HeLa cells across laboratories.

Yansheng Liu, Yang Mi, Torsten Mueller, Saskia Kreibich, Evan G Williams, Audrey Van Drogen, Christelle Borel, Max Frank, Pierre-Luc Germain, Isabell Bludau and 13 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature biotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 193 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
193citing papers in PubMed, 3 pooled it
17.9field-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

193 citing papers in PubMed, 3 syntheses or guidelines pooled it, 362 citations in OpenAlex.

  1. Pooled it
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  7. An Integrated DNA Nanoprobe for Intranuclear Imaging and In Situ Profiling of OGG1 Activity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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133 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

23 authors at 11 institutions in 5 countries.

Yansheng LiuDepartment of Pharmacology, Yale University School of Medicine, New Haven, CT, USA. yansheng.liu@yale.edu.
Yang Mi *Heidelberg University, Faculty of Biosciences, Heidelberg, Germany.ORCID http://orcid.org/0000-0003-0366-4390
Torsten Mueller *Department of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Saskia Kreibich *Institute of Microbiology, ETH Zurich, Zurich, Switzerland.
Evan G WilliamsDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Audrey Van DrogenDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Christelle BorelDepartment of Genetic Medicine and Development, University of Geneva Medical School, and University Hospitals of Geneva, Geneva, Switzerland.
Max FrankDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Pierre-Luc GermainIEO, European Institute of Oncology IRCCS, Milan, Italy.ORCID http://orcid.org/0000-0003-3418-4218
Isabell BludauDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-2601-238X
Martin MehnertDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Michael SeifertInstitute for Medical Informatics and Biometry, Carl Gustav Carus Faculty of Medicine, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-2844-053X
Mario EmmenlauerBiozentrum, University of Basel, Basel, Switzerland.
Isabel SorgBiozentrum, University of Basel, Basel, Switzerland.
Fedor BezrukovDepartment of Genetic Medicine and Development, University of Geneva Medical School, and University Hospitals of Geneva, Geneva, Switzerland.
Frederique Sloan BenaService of Genetic Medicine, University Hospitals of Geneva, Geneva, Switzerland.
Hu ZhouDepartment of Analytical Chemistry and CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.ORCID http://orcid.org/0000-0001-7006-4737
Christoph DehioBiozentrum, University of Basel, Basel, Switzerland.
Giuseppe TestaIEO, European Institute of Oncology IRCCS, Milan, Italy.
Julio Saez-RodriguezJoint Research Center for Computational Biomedicine (JRC-COMBINE), Faculty of Medicine, RWTH Aachen University, Aachen, Germany.ORCID http://orcid.org/0000-0002-8552-8976
Stylianos E AntonarakisDepartment of Genetic Medicine and Development, University of Geneva Medical School, and University Hospitals of Geneva, Geneva, Switzerland.
Wolf-Dietrich HardtInstitute of Microbiology, ETH Zurich, Zurich, Switzerland.
Ruedi AebersoldDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland. aebersold@imsb.biol.ethz.ch.ORCID http://orcid.org/0000-0002-9576-3267
ETH Zurich · CHUniversity of Basel · CHUniversity of Geneva · CHHeidelberg University · DEChinese Academy of Sciences · CNEuropean Institute of Oncology · ITNational Center for Tumor Diseases · DEUniversity Hospital of Geneva · CHUniversity of Milan · ITUniversity of Zurich · CHYale Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reproducibility in research can be compromised by both biological and technical variation, but most of the focus is on removing the latter. Here we investigate the effects of biological variation in HeLa cell lines using a systems-wide approach. We determine the degree of molecular and phenotypic variability across 14 stock HeLa samples from 13 international laboratories. We cultured cells in uniform conditions and profiled genome-wide copy numbers, mRNAs, proteins and protein turnover rates in each cell line. We discovered substantial heterogeneity between HeLa variants, especially between lines of the CCL2 and Kyoto varieties, and observed progressive divergence within a specific cell line over 50 successive passages. Genomic variability has a complex, nonlinear effect on transcriptome, proteome and protein turnover profiles, and proteotype patterns explain the varying phenotypic response of different cell lines to Salmonella infection. These findings have implications for the interpretation and reproducibility of research results obtained from human cultured cells.

Indexed as

HeLa CellsDNA Copy Number VariationsGenome, HumanGenomicsHumansProteomeReproducibility of ResultsTranscriptomeProteome

Identifiers

PMID30778230
OpenAlexW2912937988

What OpenQuestion holds

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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.