Evidence map›Paper›PMID 28126923›Full record

ArticleNucleic acids research2017

Bisulfite-independent analysis of CpG island methylation enables genome-scale stratification of single cells.

Lin Han, Hua-Jun Wu, Haiying Zhu, Kun-Yong Kim, Sadie L Marjani, Markus Riester, Ghia Euskirchen, Xiaoyuan Zi, Jennifer Yang, Jasper Han and 7 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–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

36 citing papers in PubMed.

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  9. Single-cell Technologies Provide Novel Insights into Liver Physiology and Pathology.Journal of clinical and translational hepatology · 2024
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  16. Computational Methods for Single-cell DNA Methylome Analysis.Genomics, proteomics & bioinformatics · 2023
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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

17 authors.

Lin HanDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.
Hua-Jun WuDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Haiying ZhuDepartment of Genetics, Yale School of Medicine, New Haven, CT 06520, USA.
Kun-Yong KimDepartment of Genetics, Yale Stem Cell Center, Yale School of Medicine, 10 Amistad, 201B, New Haven, CT 06520, USA.
Sadie L MarjaniDepartment of Genetics, Yale School of Medicine, New Haven, CT 06520, USA.
Markus RiesterDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Ghia EuskirchenDepartment of Genetics, Stanford University, Palo Alto, CA 94305, USA.
Xiaoyuan ZiDepartment of Genetics, Yale School of Medicine, New Haven, CT 06520, USA.
Jennifer YangDepartment of Genetics, Yale School of Medicine, New Haven, CT 06520, USA.
Jasper HanDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.
Michael SnyderDepartment of Genetics, Stanford University, Palo Alto, CA 94305, USA.
In-Hyun ParkDepartment of Genetics, Yale Stem Cell Center, Yale School of Medicine, 10 Amistad, 201B, New Haven, CT 06520, USA.
Rafael IrizarryDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Sherman M WeissmanDepartment of Genetics, Yale School of Medicine, New Haven, CT 06520, USA.
Franziska MichorDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Rong FanDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.
Xinghua PanDepartment of Genetics, Yale School of Medicine, New Haven, CT 06520, USA.

Funding

Special EquipmentP50HG007735 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2014 to 2018
$15.2M
Project 3: Single Cell Measures of Intratumor Diversity for Optimal Breast Cancer TherapyU54CA193461 · NCI · DANA-FARBER CANCER INST · PI POLYAK, KORNELIA · 2015 to 2020
$11.2M
Integrative Omics as a Discovery Tool for Pulmonary HypertensionR01HL122887 · NHLBI · STANFORD UNIVERSITY · PI NICOLLS, MARK ROBERT, RABINOVITCH, MARLENE · 2015 to 2018
$4.1M
NCI NIH HHS U54 CA193461NHGRI NIH HHS P50 HG007735NHLBI NIH HHS R01 HL122887
6 · The paper itself

Abstract

Conventional DNA bisulfite sequencing has been extended to single cell level, but the coverage consistency is insufficient for parallel comparison. Here we report a novel method for genome-wide CpG island (CGI) methylation sequencing for single cells (scCGI-seq), combining methylation-sensitive restriction enzyme digestion and multiple displacement amplification for selective detection of methylated CGIs. We applied this method to analyzing single cells from two types of hematopoietic cells, K562 and GM12878 and small populations of fibroblasts and induced pluripotent stem cells. The method detected 21 798 CGIs (76% of all CGIs) per cell, and the number of CGIs consistently detected from all 16 profiled single cells was 20 864 (72.7%), with 12 961 promoters covered. This coverage represents a substantial improvement over results obtained using single cell reduced representation bisulfite sequencing, with a 66-fold increase in the fraction of consistently profiled CGIs across individual cells. Single cells of the same type were more similar to each other than to other types, but also displayed epigenetic heterogeneity. The method was further validated by comparing the CpG methylation pattern, methylation profile of CGIs/promoters and repeat regions and 41 classes of known regulatory markers to the ENCODE data. Although not every minor methylation differences between cells are detectable, scCGI-seq provides a solid tool for unsupervised stratification of a heterogeneous cell population.

Indexed as

CpG IslandsDNA MethylationEpigenesis, GeneticPromoter Regions, GeneticCell LineCell Line, TumorChromosome MappingDNA Restriction EnzymesFibroblastsGenetic VariationGenome, HumanHigh-Throughput Nucleotide SequencingHumansInduced Pluripotent Stem CellsK562 CellsLymphocytesDNA Restriction Enzymes

Identifiers

PMID28126923
PMCPMC5605247

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.