Evidence map›Paper›PMID 22586076›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Real-time analysis and selection of methylated DNA by fluorescence-activated single molecule sorting in a nanofluidic channel.

Benjamin R Cipriany, Patrick J Murphy, James A Hagarman, Aline Cerf, David Latulippe, Stephen L Levy, Jaime J Benítez, Christine P Tan, Juraj Topolancik, Paul D Soloway and 1 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Quantitative characterization of liquids flowing in geometrically controlled sub-100 nm nanofluidic channels.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2023
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Single-molecule DNA-mapping and whole-genome sequencing of individual cells.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  10. Review
  11. Article
  12. Article
  13. Single molecule and single cell epigenomics.Methods (San Diego, Calif.) · 2015
    Review
  14. Article
  15. Review
  16. Review
  17. Epigenomics: one molecule at a time.Cell cycle (Georgetown, Tex.) · 2013
    Article
  18. Review
  19. Article
  20. Single-molecule analysis of combinatorial epigenomic states in normal and tumor cells.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Benjamin R CiprianyDepartment of Electrical and Computer Engineering, Cornell University, Ithaca, NY 14853, USA.
Patrick J Murphy
James A Hagarman
Aline Cerf
David Latulippe
Stephen L Levy
Jaime J Benítez
Christine P Tan
Juraj Topolancik
Paul D Soloway
Harold G Craighead

Funding

TRANS-NETWORK PROJECTSU54CA143876 · NCI · CORNELL UNIVERSITY · PI SHULER, MICHAEL L · 2009 to 2014
$12.6M
Reproductive Sciences and Genomics Training ProgramT32HD052471 · NICHD · CORNELL UNIVERSITY · PI ROBERSON, MARK S · 2007 to 2016
$2.0M
Epigenomic analysis on a nanoscale deviceR01DA025722 · NIDA · CORNELL UNIVERSITY · PI CRAIGHEAD, HAROLD G, SOLOWAY, PAUL D · 2008 to 2011
$1.5M
Epigenetic Control of a Ras ActivatorR01GM105243 · NIGMS · CORNELL UNIVERSITY · PI SOLOWAY, PAUL D · 2013 to 2016
$1.3M
NCI NIH HHS U54 CA143876NCI NIH HHS U54CA143876NICHD NIH HHS T32 HD052471NIDA NIH HHS DA025722NIDA NIH HHS R01 DA025722NIGMS NIH HHS R01 GM105243
6 · The paper itself

Abstract

Epigenetic modifications, such as DNA and histone methylation, are responsible for regulatory pathways that affect disease. Current epigenetic analyses use bisulfite conversion to identify DNA methylation and chromatin immunoprecipitation to collect molecules bearing a specific histone modification. In this work, we present a proof-of-principle demonstration for a new method using a nanofluidic device that combines real-time detection and automated sorting of individual molecules based on their epigenetic state. This device evaluates the fluorescence from labeled epigenetic modifications to actuate sorting. This technology has demonstrated up to 98% accuracy in molecule sorting and has achieved postsorting sample recovery on femtogram quantities of genetic material. We have applied it to sort methylated DNA molecules using simultaneous, multicolor fluorescence to identify methyl binding domain protein-1 (MBD1) bound to full-duplex DNA. The functionality enabled by this nanofluidic platform now provides a workflow for color-multiplexed detection, sorting, and recovery of single molecules toward subsequent DNA sequencing.

Indexed as

DNA MethylationDNADNA-Binding ProteinsFluorescenceHumansMicrofluidic Analytical TechniquesMicroscopy, ConfocalNanotechnologyProtein BindingReal-Time Polymerase Chain ReactionReproducibility of ResultsTime FactorsTranscription FactorsDNADNA-Binding ProteinsMBD1 protein, humanTranscription Factors

Identifiers

PMID22586076
PMCPMC3365150

What OpenQuestion holds

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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.