2001
DOI: 10.1007/bf03262045
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Ramification Amplification: A Novel Isothermal DNA Amplification Method

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Cited by 14 publications
(4 citation statements)
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“…Concurrently, a distinct category of WGA techniques embodies isothermal methodologies. Preeminently, Multiple Displacement Amplification (MDA) reigns as the paradigmatic approach, characterized by isothermal random priming and extension orchestrated by φ29 polymerase, distinguished by its robust catalytic activity, minimal error propensity, and strand displacement competence [60,63]. Owing to φ29 polymerase's elevated fidelity, these techniques manifest augmented genome coverage vis-à-vis initial PCR-based methods, accompanied by mitigated error rates.…”
Section: /14mentioning
confidence: 99%
“…Concurrently, a distinct category of WGA techniques embodies isothermal methodologies. Preeminently, Multiple Displacement Amplification (MDA) reigns as the paradigmatic approach, characterized by isothermal random priming and extension orchestrated by φ29 polymerase, distinguished by its robust catalytic activity, minimal error propensity, and strand displacement competence [60,63]. Owing to φ29 polymerase's elevated fidelity, these techniques manifest augmented genome coverage vis-à-vis initial PCR-based methods, accompanied by mitigated error rates.…”
Section: /14mentioning
confidence: 99%
“…For single-cell isolation, various methods can be employed, each with different levels of accuracy, throughput, reproducibility, and usability. 74,75 Whole-genome amplification (WGA) approaches, such as degenerate oligonucleotide-primed PCR, 76,77 multiple displacement amplification, 78,79 multiple annealing and looping-based amplification cycles, and PicoPLEX, 80,81 can be utilized to amplify DNA before sequencing. Microfluidic devices have shown promise in reducing contamination during single-cell WGA, 82 and a novel two-step microfluidic droplet program has been proposed to realize efficient and large-scale parallel barcoding based on single-cell PCR.…”
Section: Single-cell Sequencing For Genomes (Scdna-seq)mentioning
confidence: 99%
“…Rolling circle amplification was first developed as a method in the mid-1990s ( 7 11 ). A typical application of rolling circle amplification is generating long, single-stranded DNA concatemers as the template for long-read sequencing as with Oxford Nanopore Technologies (ONT) platforms, allowing error correction by taking a consensus of the de-concatenated sequence ( 12 ).…”
Section: Introductionmentioning
confidence: 99%