ArticleNucleic acids research2009
A single molecule array for digital targeted molecular analyses.
Article in Nucleic acids research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- ddRFC: A scalable multiplexed droplet digital nucleic acid amplification test platform.Biosensors & bioelectronics · 2020Article
- Sensitive and inexpensive digital DNA analysis by microfluidic enrichment of rolling circle amplified single-molecules.Nucleic acids research · 2017Article
- Let There Be Light!Proteomes · 2016Review
- In situ mutation detection and visualization of intratumor heterogeneity for cancer research and diagnostics.Oncotarget · 2013Article
- Assessing the stochastic intermittency of single quantum dot luminescence for robust quantification of biomolecules.Analytical chemistry · 2013Article
- Parallel visualization of multiple protein complexes in individual cells in tumor tissue.Molecular & cellular proteomics : MCP · 2013Article
- Selective cell capture and analysis using shallow antibody-coated microchannels.Biomicrofluidics · 2012Article
- Single molecule analysis of combinatorial splicing.Nucleic acids research · 2010Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We present a new random array format together with a decoding scheme for targeted multiplex digital molecular analyses. DNA samples are analyzed using multiplex sets of padlock or selector probes that create circular DNA molecules upon target recognition. The circularized DNA molecules are amplified through rolling-circle amplification (RCA) to generate amplified single molecules (ASMs). A random array is generated by immobilizing all ASMs on a microscopy glass slide. The ASMs are identified and counted through serial hybridizations of small sets of tag probes, according to a combinatorial decoding scheme. We show that random array format permits at least 10 iterations of hybridization, imaging and dehybridization, a process required for the combinatorial decoding scheme. We further investigated the quantitative dynamic range and precision of the random array format. Finally, as a demonstration, the decoding scheme was applied for multiplex quantitative analysis of genomic loci in samples having verified copy-number variations. Of 31 analyzed loci, all but one were correctly identified and responded according to the known copy-number variations. The decoding strategy is generic in that the target can be any biomolecule which has been encoded into a DNA circle via a molecular probing reaction.
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Registered trials
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.