2003
DOI: 10.1073/pnas.1133470100
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Transforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variations

Abstract: Many areas of biomedical research depend on the analysis of uncommon variations in individual genes or transcripts. Here we describe a method that can quantify such variation at a scale and ease heretofore unattainable. Each DNA molecule in a collection of such molecules is converted into a single magnetic particle to which thousands of copies of DNA identical in sequence to the original are bound. This population of beads then corresponds to a one-to-one representation of the starting DNA molecules. Variation… Show more

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Cited by 727 publications
(491 citation statements)
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References 29 publications
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“…This oligonucleotide was coupled to streptavidin-coated magnetic beads (MyOne, Dynal, Oslo) according to the protocol described in ref. 16. The water-in-oil emulsions were prepared by modifications of the methods described by Ghadessy and Holliger (17) 5 per l oligonucleotide-coupled beads, and 0.1 pg͞ l template DNA.…”
Section: Methodsmentioning
confidence: 99%
“…This oligonucleotide was coupled to streptavidin-coated magnetic beads (MyOne, Dynal, Oslo) according to the protocol described in ref. 16. The water-in-oil emulsions were prepared by modifications of the methods described by Ghadessy and Holliger (17) 5 per l oligonucleotide-coupled beads, and 0.1 pg͞ l template DNA.…”
Section: Methodsmentioning
confidence: 99%
“…Emulsion PCR was performed according to Dressman et al (2003) with a few minor modifications (Supplement Emulsion Methods). Since limited dilution of DNA is utilized to produce clonal bead amplification, 70%-80% of the beads in any given emulsion are unamplified beads.…”
Section: Fragment Librariesmentioning
confidence: 99%
“…BEAMing was named after its components-beads, emulsions, amplification, and magnetics-and essentially converts single DNA template molecules to single beads containing tens of thousands of exact copies of the template. 6 We used this method to determine how frequently mutations could be detected in the DNA from plasma or stool of the same patients as well as to investigate other parameters that could be useful in designing clinically applicable DNA-based tests in the future.…”
mentioning
confidence: 99%