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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

Rapid routine detection of enterovirus RNA in cerebrospinal fluid by a one-step real-time RT-PCR assay

TL;DR: The new TM-PCR is a convincing alternative to conventional PCR protocols for the diagnosis of enterovirus meningitis because the one-step strategy limits hands on time and cross contamination risk combined with accelerated assay procedure of only 100 min.
Journal ArticleDOI

High frequency of human papillomavirus infection in carcinoma of the urinary bladder.

TL;DR: The prevalence of type 6, 11, 16, 18, and 33 human papillomavirus (HPV) was investigated with the polymerase chain reaction (PCR) on formalin‐fixed, paraffin wax‐embedded material, including 48 neoplastic and 21 normal urinary bladder specimens.
Journal ArticleDOI

Molecular evidence of organ-related transmission of Kaposi sarcoma-associated herpesvirus or human herpesvirus-8 in transplant patients.

TL;DR: The 100% identity of nucleotide sequence of the most variable viral region and the presence of the same, single orf -73 type in both patients provides strong molecular evidence of organ-related transmission of HHV-8 in the setting of transplantation.
Journal ArticleDOI

The predominance of hepatitis delta virus genotype I among chronically infected Italian patients.

TL;DR: It is concluded that in Italy, where HDV infection has been endemic, the overwhelmingly predominant genotype of HDV is genotype I, and this genotype appeared to be associated with a broad spectrum of chronic disease.
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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