نتایج جستجو برای: and ngs

تعداد نتایج: 16827872  

2014
Yoshiki Murakami Toshihito Tanahashi Rina Okada Hidenori Toyoda Takashi Kumada Masaru Enomoto Akihiro Tamori Norifumi Kawada Y-h Taguchi Takeshi Azuma

MicroRNA (miRNA) expression profiling has proven useful in diagnosing and understanding the development and progression of several diseases. Microarray is the standard method for analyzing miRNA expression profiles; however, it has several disadvantages, including its limited detection of miRNAs. In recent years, advances in genome sequencing have led to the development of next-generation seque...

2018
Jochen Singer Hans-Joachim Ruscheweyh Ariane L. Hofmann Thomas Thurnherr Franziska Singer Nora C. Toussaint Charlotte K. Y. Ng Salvatore Piscuoglio Christian Beisel Gerhard Christofori Reinhard Dummer Michael N. Hall Wilhelm Krek Mitchell P. Levesque Markus G. Manz Holger Moch Andreas Papassotiropoulos Daniel J. Stekhoven Peter Wild Thomas Wüst Bernd Rinn Niko Beerenwinkel

Motivation Next-generation sequencing is now an established method in genomics, and massive amounts of sequencing data are being generated on a regular basis. Analysis of the sequencing data is typically performed by lab-specific in-house solutions, but the agreement of results from different facilities is often small. General standards for quality control, reproducibility and documentation are...

2018
Ari Vanderwalde David Spetzler Nianqing Xiao Zoran Gatalica John Marshall

Microsatellite instability (MSI) testing identifies patients who may benefit from immune checkpoint inhibitors. We developed an MSI assay that uses data from a commercially available next-generation sequencing (NGS) panel to determine MSI status. The assay is applicable across cancer types and does not require matched samples from normal tissue. Here, we describe the MSI-NGS method and explore ...

2010
Paul Richardson

Next Generation Sequencing (NGS) refers to technologies that do not rely on traditional dideoxy-nucleotide (Sanger) sequencing where labeled DNA fragments are physically resolved by electrophoresis. These new technologies rely on different strategies, but essentially all of them make use of real-time data collection of a base level incorporation event across a massive number of reactions (on th...

Journal: :Investigative ophthalmology & visual science 2016
Thomas Wecker Klaus Hoffmeier Anne Plötner Björn Andreas Grüning Ralf Horres Rolf Backofen Thomas Reinhard Günther Schlunck

PURPOSE Extracellular microRNAs (miRNAs) in aqueous humor were suggested to have a role in transcellular signaling and may serve as disease biomarkers. The authors adopted next-generation sequencing (NGS) techniques to further characterize the miRNA profile in single samples of 60 to 80 μL human aqueous humor. METHODS Samples were obtained at the outset of cataract surgery in nine independent...

Journal: :Journal of medical genetics 2012
James O'Sullivan Brendan G Mullaney Sanjeev S Bhaskar Jonathan E Dickerson Georgina Hall Anna O'Grady Andrew Webster Simon C Ramsden Graeme C Black

OBJECTIVES Current technologies for delivering gene testing are labour-intensive and expensive. Over the last 3 years, new high-throughput DNA sequencing techniques (next generation sequencing; NGS), with the capability to analyse multiple genes or entire genomes, have been rapidly adopted into research. This study examines the possibility of incorporating NGS into a clinical UK service context...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2013
Fiamma Buttitta Lara Felicioni Maela Del Grammastro Giampaolo Filice Alessia Di Lorito Sara Malatesta Patrizia Viola Irene Centi Tommaso D'Antuono Roberta Zappacosta Sandra Rosini Franco Cuccurullo Antonio Marchetti

PURPOSE The therapeutic choice for patients with lung adenocarcinoma depends on the presence of EGF receptor (EGFR) mutations. In many cases, only cytologic samples are available for molecular diagnosis. Bronchoalveolar lavage (BAL) and pleural fluid, which represent a considerable proportion of cytologic specimens, cannot always be used for molecular testing because of low rate of tumor cells....

2016
Jiawei Xu Wenbin Niu Zhaofeng Peng Xiao Bao Meixiang Zhang Linlin Wang Linqing Du Nan Zhang Yingpu Sun

Triploidy occurred about 2-3% in human pregnancies and contributed to approximately 15% of chromosomally caused human early miscarriage. It is essential for preimplantation genetic diagnosis and screen to distinct triploidy sensitively. Here, we performed comparative investigations between MALBAC-NGS and MDA-SNP array sensitivity on triploidy detection. Self-correction and reference-correction ...

2016
Catherine W. Bennett Guy Berchem Yeoun Jin Kim Victoria El-Khoury

Personalized medicine has emerged as the future of cancer care to ensure that patients receive individualized treatment specific to their needs. In order to provide such care, molecular techniques that enable oncologists to diagnose, treat, and monitor tumors are necessary. In the field of lung cancer, cell free DNA (cfDNA) shows great potential as a less invasive liquid biopsy technique, and n...

Journal: :Progress in Retinal and Eye Research 2016
Vijender Chaitankar Gökhan Karakülah Rinki Ratnapriya Felipe O. Giuste Matthew J. Brooks Anand Swaroop

The advent of high throughput next generation sequencing (NGS) has accelerated the pace of discovery of disease-associated genetic variants and genomewide profiling of expressed sequences and epigenetic marks, thereby permitting systems-based analyses of ocular development and disease. Rapid evolution of NGS and associated methodologies presents significant challenges in acquisition, management...

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