使用期限*
许可形式单机
原产地美国
介质下载
适用平台windows,mac
科学软件网销售软件达19年,有丰富的销售经验以及客户资源,提供的产品涵盖各个学科,包括经管,仿真,地球地理,生物化学,工程科学,排版及网络管理等。此外,我们还提供很多附加服务,如:现场培训、课程、解决方案、咨询服务等。
Sequencher DNA序列分析软件是科学家们*的工具。持续发展和改进**过25年,Sequencher提供了**的功能特征,成千上万的出版物都有相关的应用介绍。新手用户可以以少的时间投资产生结果,而有经验的用户会惊叹于功能的深度和控制。Sequencher自带各种专有算法,可以为Sanger, Next-Gen Sequencing (NGS)和RNA-Seq序列数据生成结果。
SNP检测
Sequencher有几个强大的工具来帮助你检测DNA序列中的突变和单核苷酸多态性。您可以使用Sequencher来对一组序列之间的比较序列比对或将1个或多个序列与参考序列进行比较。Sequencher的Call Secondary Peaks...功能分析您所有的潜在杂合子序列。控制杂合子的严格性是很*的。
您可以从一个杂合子导航到下一个,只需单击Basic视图中的空格键即可。查看蛋白质转换对于共识和参考序列低于共识。参考序保SNP的编号从一个DNA组件到下一个DNA组件是一致的。

We have continued our strategy of adding functionality to Sequencher that focuses on labs doing DNA sequencing. Unlike many companies in this field, we are continuing work on improving the productivity and utility of Sanger sequencing based on feedback from our collaborators around the world, and focusing on smoothly integrating those features with the latest tools for next-generation DNA sequence alignment. If you work in a lab that supports NGS, you must already have information technology [I. T.] support, but our mission is to make the data and analysis of ALL sequencing data accessible and understandable to life scientists without requiring that they have a degree in computer engineering.

Automated Analysis
Sequencher batch processes your DNA sequence data in a way that is transparent, user definable, and recoverable, and Sequencher never jeopardizes the validity of your scientific conclusions for the sake of automation. Sequencher always gives you the final choice in your sequence editing.

Sequence Trimming
Automated DNA sequencers occasionally produce poor quality reads, particularly near the sequencing primer site, and toward the end of longer sequence runs. The sequences of clones from DNA libraries frequently contain vector sequence, polyA tails, or other unrelated sequence. Introns and primer sequence frequently flank the sequence of amplified exons. Unless removed by trimming, any of these artifacts will distort your sequence assembly and downstream sequence analysis.
19年来,公司始终秉承、专注、专心的发展理念,厚积薄发,积累了大量的人才、技术以及行业经验,在行业内得到了大量用户的认可和高度价。
http://turntech8843.b2b168.com