Next Generation sequencing or NGS, is massively parallel, high throughput DNA sequencing.
新一代测序也被称为NGS，指的是大规模平行和高通量dna测序。
He concluded that next generation sequencing will impact our knowledge about tumor behavior and have direct translational potential.
他推断下一步基因测序将会对我们对肿瘤行为知识产生影响，有直接翻译能力。
"If somebody is to get the Nobel Prize for next-generation sequencing, it should be Jonathan," said Michael Weiner, who worked for Dr. Rothberg for many years.
“如果有人能为下一代测序诺贝尔奖，它应该是乔纳森，”迈克尔说韦纳，谁博士rothberg工作多年。
An international team of researchers from Leeds, London and Berlin has discovered more about the function of muscle stem cells, thanks to next-generation DNA sequencing techniques.
来自利兹大学、伦敦大学和德国柏林大学组成的一个国际研究团队近日发现，肌肉干细胞的更多功能，这得益于下一代DNA测序技术。
We also combined micro arrays and next-generation sequencing data for validation.
我们同时也结合芯片和下一代测序数据作为校验。
The tools are extremely efficient and allow the user to compare large datasets (e. g., next-generation sequencing data) with both public and custom genome annotation tracks.
该工具特别高效，并允许用户用公开的和定制的基因组注释轨道比较大的数据集(例如，下一代测序数据)。
This paper looked at molecular changes in a large number of MDS patients using up-to-date molecular techniques, including next-generation sequencing and mass spectrometry genome typing.
该文应用现代分子技术(包括下一代测序技术及质谱基因组分型)寻找大mds患者样本中的分子改变。
However, at present, the analysis of next-generation sequencing data is challenging, in particular because most sequencing platforms provide short reads, which are difficult to align and assemble.
然而，目前，下一代测序数据的分析仍然面临挑战，尤其是大多数测序平台产生了短序列，这对比对和组装造成了困难。
These data are generated by the research community using high-throughput technologies like microarrays and, more recently, next-generation sequencing.
这些数据是由研究团体使用高通量技术产生的，像微阵列技术，和最近的，下一代测序。
We present performance characteristics of a next-generation sequencing assay designed to detect such mutations.
本文介绍用来检测这些突变的新一代测序分析性能特点。
According to the firm, the approval is the first for a next-generation sequencing system in Canada.
根据该公司的说法，这是加拿大第一次批准下一代测序系统。
Next-generation sequencing showed precise measurement of mutant allele frequencies and detected 23% of mutations with 2-20% mutant allele frequencies.
新一代测序技术对等位基因特异性突变几率非常精确，检测出了23%的基因突变、其中等位基因突变的几率达2- 20%。
Herein, we report a unique case of metastatic basal cell carcinosarcoma, in which we analyzed the 2 components of the primary tumor as well as the metastasis by next-generation sequencing.
我们报道的唯一一例转移性基底细胞癌肉瘤病例，并对原发肿瘤的两种成分及转移成分进行了第二代基因测序。
In addition, only little is known about sources of variation that are associated with next-generation sequencing study designs.
此外，下一代测序研究设计中变异的相关信息也所知甚少。
In addition, only little is known about sources of variation that are associated with next-generation sequencing study designs.
此外，下一代测序研究设计中变异的相关信息也所知甚少。
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