نتایج جستجو برای: نمودار پرتوزایی گامای طبیعی ngs

تعداد نتایج: 60005  

داوود جمالی اسفهلان محمدتقی طهماسب نظامی محمدرضا قادری,

 برای ارزیابی کمی عیار اورانیوم گمانه‌های حفاری شده در کانسار خشومی، از داده‌های چاه‌پیمایی و آزمایشگاهی XRF نمونه‌های مغزه استفاده می‌شود. بنابراین برای تعیین رابطة این دو نوع داده، با تقسیم محدوده‌ مغزه‌های گمانه‌ها به فواصل 3.05  متری معادل فواصل بین پلاک‌های حفاری، عملیات یکسان‌سازی و آنالیز داده‌های چاه‌پیمایی در 115 محدوده انجام پذیرفت و از میان آنها، 55 محدوده که دارای ضریب بازیابی مغزه ...

2013
Satoshi Narumi Kumihiro Matsuo Tomohiro Ishii Yusuke Tanahashi Tomonobu Hasegawa

Somatic activating GNAS mutations cause McCune-Albright syndrome (MAS). Owing to low mutation abundance, mutant-specific enrichment procedures, such as the peptide nucleic acid (PNA) method, are required to detect mutations in peripheral blood. Next generation sequencing (NGS) can analyze millions of PCR amplicons independently, thus it is expected to detect low-abundance GNAS mutations quantit...

2017
Dan Su Dadong Zhang Kaiyan Chen Jing Lu Junzhou Wu Xinkai Cao Lisha Ying Qihuang Jin Yizhou Ye Zhenghua Xie Lei Xiong Weimin Mao Fugen Li

BACKGROUND Next generation sequencing (NGS) is being increasingly applied for assisting cancer molecular diagnosis. However, it is still needed to validate NGS accuracy on detection of DNA alternations based on a large number of clinical samples, especially for DNA rearrangements and copy number variations (CNVs). This study is to set up basic parameters of targeted NGS for clinical diagnosis a...

2016
Rosa A van Amerongen Valesca P Retèl Veerle MH Coupé Petra M Nederlof Maartje J Vogel Wim H van Harten

Next-generation sequencing (NGS) has reached the molecular diagnostic laboratories. Although the NGS technology aims to improve the effectiveness of therapies by selecting the most promising therapy, concerns are that NGS testing is expensive and that the 'benefits' are not yet in relation to these costs. In this study, we give an estimation of the costs and an institutional and national budget...

2017
Saeam Shin In Sik Hwang Jieun Kim Kyung-A Lee Seung-Tae Lee Jong Rak Choi

Minimal residual disease (MRD) following B-lymphoblastic leukemia (B-ALL) treatment has gained prognostic importance. Clonal immunoglobulin heavy chain (IGH) gene rearrangement is a useful follow-up marker in B-ALL owing to its high positivity rate. We evaluated the performance and clinical applicability of a next-generation sequencing (NGS) assay for IGH rearrangement in B-ALL MRD monitoring. ...

2016
Ki Ho Hong Sung Kuk Hong Sung Im Cho Eunkyung Ra Kyung Hee Han Soon Beom Kang Eui-Chong Kim Sung Sup Park Moon-Woo Seong

BACKGROUND Next-generation sequencing (NGS) can detect many more microorganisms of a microbiome than traditional methods. This study aimed to analyze the vaginal microbiomes of Korean women by using NGS that included bacteria and other microorganisms. The NGS results were compared with the results of other assays, and NGS was evaluated for its feasibility for predicting vaginitis. METHODS In ...

Journal: :Cancer informatics 2015
Jian Li Aarif Mohamed Nazeer Batcha Björn Grüning Ulrich R Mansmann

Next-generation sequencing (NGS) technologies that have advanced rapidly in the past few years possess the potential to classify diseases, decipher the molecular code of related cell processes, identify targets for decision-making on targeted therapy or prevention strategies, and predict clinical treatment response. Thus, NGS is on its way to revolutionize oncology. With the help of NGS, we can...

2016
Ernst Joachim Houtgast Vlad-Mihai Sima Koen Bertels Zaid Al-Ars

We are rapidly entering the era of genomics. The dramatic cost reduction of DNA sequencing due to the introduction of Next Generation Sequencing (NGS) techniques has resulted in an exponential growth of genetics data. The amount of data generated, and its associated processing into useful information, poses serious computational challenges. Here, we give a brief introduction of NGS, show a typi...

2014
Saumya Pant Russell Weiner Matthew J. Marton

Over the past decade, next-generation sequencing (NGS) technology has experienced meteoric growth in the aspects of platform, technology, and supporting bioinformatics development allowing its widespread and rapid uptake in research settings. More recently, NGS-based genomic data have been exploited to better understand disease development and patient characteristics that influence response to ...

2013
Alexander Eiler Stina Drakare Stefan Bertilsson Jakob Pernthaler Sari Peura Carina Rofner Karel Simek Yang Yang Petr Znachor Eva S. Lindström

The recognition and discrimination of phytoplankton species is one of the foundations of freshwater biodiversity research and environmental monitoring. This step is frequently a bottleneck in the analytical chain from sampling to data analysis and subsequent environmental status evaluation. Here we present phytoplankton diversity data from 49 lakes including three seasonal surveys assessed by n...

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