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Journal ArticleDOI

Avoiding false positives with PCR

S Kwok, +1 more
- 18 May 1989 - 
- Vol. 339, Iss: 6221, pp 237-238
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TLDR
The exquisite sensitivity of the polymerase chain reaction means DNA contamination can ruin an entire experiment and adherence to a strict set of protocols can avoid disaster.
Abstract
The exquisite sensitivity of the polymerase chain reaction means DNA contamination can ruin an entire experiment. Tidiness and adherence to a strict set of protocols can avoid disaster.

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Citations
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Journal ArticleDOI

Bacteriological and PCR analysis of clinical material aspirated from otitis media with effusions.

TL;DR: It is demonstrated that effusion fluid from otitis media cases contain a battery of bacterial species and these bacteria might play roles in the pathogens of OME.
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A multicenter randomized controlled trial of recombinant interferon‐α2b in patients with acute transfusion‐associated hepatitis C

TL;DR: One major finding was that short‐term treatment with interferon‐α was effective in most patients with acute hepatitis C and led to complete recovery from hepatitis in 39 of the cases.
Journal ArticleDOI

Comparison between PCR and Detection of Antigen in Sera for Diagnosis of Pulmonary Aspergillosis

TL;DR: D detection of Aspergillus DNA in serum samples by nested PCR had the highest sensitivity of the three methods tested for the diagnosis of pulmonary aspergillosis.
Journal ArticleDOI

Single-molecule electrophoresis

TL;DR: In this paper, a novel method for the detection and identification of single molecules in solution has been devised, computer simulated, and experimentally achieved, which involves the determination of electrophoretic velocities by measuring the time required for individual molecules to travel a fixed distance between two laser beams.
Journal ArticleDOI

Hepatitis C virus infection in kidney transplant recipients

TL;DR: The data suggest that the prevalence of hepatitis Cirus infection is high in kidney transplant recipients, active hepatitis C virus replication may be present in the absence of hepatitisC virus antibody, and many of these patients who are second‐generation enzyme immunoassay–positive but second‐ generation recombinant immunoblot assay–indeterminate are hepatitis C Virus RNA positive.
References
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Journal ArticleDOI

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

TL;DR: A thermostable DNA polymerase was used in an in vitro DNA amplification procedure, the polymerase chain reaction, which significantly improves the specificity, yield, sensitivity, and length of products that can be amplified.
Book ChapterDOI

Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction.

TL;DR: A method whereby a nucleic acid sequence can be exponentially amplified in vitro is described in the chapter, and the possibility of utilizing a heat-stable DNA polymerase is explored so as to avoid the need for addition of new enzyme after each cycle of thermal denaturation.
Journal ArticleDOI

DNA amplification for direct detection of HIV-1 in DNA of peripheral blood mononuclear cells

TL;DR: This method of DNA amplification made it possible to obtain results within 3 days, whereas virus isolation takes up to 3 to 4 weeks, and may therefore be used to complement or replace virus isolation as a routine means of determining HIV-1 infection.
Journal ArticleDOI

DNA typing from single hairs

TL;DR: Three different means of DNA typing are used for the determination of amplified DNA fragment length differences, hybridization with allele-specific oligonucleotide probes, and direct DNA sequencing on single human hairs to detect genetically variable mitochondrial and nuclear DNA sequences.
Journal ArticleDOI

Amplification and analysis of DNA sequences in single human sperm and diploid cells

TL;DR: The use of the polymerase chain reaction for analysing DNA sequences in individual diploid cells and human sperm shows that two genetic loci can be co-amplified from a single sperm, which may allow the analysis of previously inaccessible genetic phenomena.
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