Evidence map›Paper›PMID 20351689›Full record

ArticleNature biotechnology2010

High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity.

Elisa Närvä, Reija Autio, Nelly Rahkonen, Lingjia Kong, Neil Harrison, Danny Kitsberg, Lodovica Borghese, Joseph Itskovitz-Eldor, Omid Rasool, Petr Dvorak and 12 more

Abstract read
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In one paragraph

Article in Nature biotechnology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed
22.0field-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

147 citing papers in PubMed, 282 citations in OpenAlex.

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  15. Human stem cell models for Marfan syndrome: aFrontiers in cell and developmental biology · 2024
    Review
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87 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 15 institutions in 7 countries.

Elisa NärväTurku Centre for Biotechnology, University of Turku and Abo Akademi University, Turku, Finland. elisa.narva@btk.fi
Reija Autio
Nelly Rahkonen
Lingjia Kong
Neil Harrison
Danny Kitsberg
Lodovica Borghese
Joseph Itskovitz-Eldor
Omid Rasool
Petr Dvorak
Outi Hovatta
Timo Otonkoski
Timo Tuuri
Wei Cui
Oliver Brüstle
Duncan Baker
Edna Maltby
Harry D Moore
Nissim Benvenisty
Peter W Andrews
Olli Yli-Harja
Riitta Lahesmaa
University of Sheffield · GBSheffield Children's NHS Foundation Trust · GBTurku Centre for Biotechnology · FIUniversity of Helsinki · FIUniversity of Turku · FIÅbo Akademi University · FIHammersmith Hospital · GBHebrew University of Jerusalem · ILKarolinska Institutet · SELife & Brain (Germany) · DEMasaryk University · CZRambam Health Care Campus · ILTampere University · FITampere University · FIUniversity of Bonn · DE

Funding

Medical Research Council G0700785Medical Research Council G0801059
6 · The paper itself

Abstract

Prolonged culture of human embryonic stem cells (hESCs) can lead to adaptation and the acquisition of chromosomal abnormalities, underscoring the need for rigorous genetic analysis of these cells. Here we report the highest-resolution study of hESCs to date using an Affymetrix SNP 6.0 array containing 906,600 probes for single nucleotide polymorphisms (SNPs) and 946,000 probes for copy number variations (CNVs). Analysis of 17 different hESC lines maintained in different laboratories identified 843 CNVs of 50 kb-3 Mb in size. We identified, on average, 24% of the loss of heterozygosity (LOH) sites and 66% of the CNVs changed in culture between early and late passages of the same lines. Thirty percent of the genes detected within CNV sites had altered expression compared to samples with normal copy number states, of which >44% were functionally linked to cancer. Furthermore, LOH of the q arm of chromosome 16, which has not been observed previously in hESCs, was detected.

Indexed as

Base SequenceCell Culture TechniquesDNADNA Copy Number VariationsDNA Mutational AnalysisEmbryonic Stem CellsGenetic VariationHumansMolecular Sequence DataSequence Analysis, DNADNA

Identifiers

PMID20351689
OpenAlexW2096910509

What OpenQuestion holds

Textmetadata
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.