نتایج جستجو برای: simple pcr

تعداد نتایج: 627586  

2018
Yoshihiko Onda Kotaro Takahagi Minami Shimizu Komaki Inoue Keiichi Mochida

Next-generation sequencing (NGS) technologies have enabled genome re-sequencing for exploring genome-wide polymorphisms among individuals, as well as targeted re-sequencing for the rapid and simultaneous detection of polymorphisms in genes associated with various biological functions. Therefore, a simple and robust method for targeted re-sequencing should facilitate genotyping in a wide range o...

2017
Konstantin A Blagodatskikh Vladimir M Kramarov Ekaterina V Barsova Alexey V Garkovenko Dmitriy S Shcherbo Andrew A Shelenkov Vera V Ustinova Maria R Tokarenko Simon C Baker Tatiana V Kramarova Konstantin B Ignatov

Whole-genome amplification (WGA) techniques are used for non-specific amplification of low-copy number DNA, and especially for single-cell genome and transcriptome amplification. There are a number of WGA methods that have been developed over the years. One example is degenerate oligonucleotide-primed PCR (DOP-PCR), which is a very simple, fast and inexpensive WGA technique. Although DOP-PCR ha...

2014
Rafael Bardera Mora

Helicopters operations on board ships require special procedures introducing additional limitations known as ship helicopter operational limitations (SHOLs) which are a priority for all navies. This paper presents the main results obtained from the experimental investigation of a simple frigate shape (SFS) which is a typical case of study in experimental and computational aerodynamics. The resu...

2010
M. Gohari H. Sharifiyazdi M. Akhlaghi

In this study the efficacy of bacterial culture, simple PCR and nested-PCR techniques for the detection of Yersinia ruckeri in tissues of naturally and experimentally infected rainbow trout (Oncorhynchus mykiss) fry was compared. In order to detect Y. ruckeri in naturally infected rainbow trout tissues, 30 fish suspected of enteric redmouth disease were randomly collected from 6 rainbow trout f...

Journal: :Transactions of the Royal Society of Tropical Medicine and Hygiene 1996
B Singh J Cox-Singh A O Miller M S Abdullah G Snounou H A Rahman

A modified nested polymerase chain reaction (PCR) method for detection of Plasmodium falciparum, P. vivax and P. malariae was combined with a simple blood collection and deoxyribonucleic acid (DNA) extraction method and evaluated in Malaysia. Finger-prick blood samples from 46 hospital patients and 120 individuals living in malaria endemic areas were spotted on filter papers and dried. The simp...

2015
Kristina Rizzardi Thomas Åkerlund

Clostridium difficile strains were typed by a newly developed MALDI-TOF method, high molecular weight typing, and compared to PCR ribotyping. Among 500 isolates representing 59 PCR ribotypes a total of 35 high molecular weight types could be resolved. Although less discriminatory than PCR ribotyping, the method is extremely fast and simple, and supports for cost-effective screening of isolates ...

Journal: :Applied and environmental microbiology 2007
Shiming Wang Jian He Zhongli Cui Shunpeng Li

We developed a self-formed adaptor PCR (termed SEFA PCR) which can be used for chromosome walking. Most of the amplified flanking sequences were longer than 2.0 kb, and some were as long as 6.0 kb. SEFA PCR is simple and efficient and should have broad applications in the isolation of unknown sequences in complex genomes.

Journal: :Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology 2003
Rory Gunson Graeme Gillespie William F Carman

In-house polymerase chain reaction (PCR) assays are now an integral part of the work of most diagnostic microbiological laboratories. Despite the availability of commercial reagent 'master-mixes' of some PCR reagents, the optimisation of primers still poses a significant problem. Here, we describe a simple method to assess the concentration of primer needed in single round, multiplex, nested an...

Journal: :Nucleic acids research 1997
K R Oldenburg K T Vo S Michaelis C Paddon

We have extended the technique of PCR-directed recombination in Saccharomyces cerevisiae to develop a simple method for plasmid or gene construction in the absence of suitable restriction sites. The DNA to be cloned is PCR-amplified with 30-40 bp of homology to a linearized yeast plasmid. Co-transformation into yeast results in homologous recombination at a position directed by the PCR oligonuc...

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