When you edit files in various formats day-to-day, the universality of the document tools matters a lot. If your instruments work for only a few of the popular formats, you might find yourself switching between application windows to copy style in binary and manage other document formats. If you wish to eliminate the headache of document editing, go for a solution that can easily manage any format.
With DocHub, you do not need to focus on anything apart from actual document editing. You will not need to juggle applications to work with diverse formats. It can help you modify your binary as easily as any other format. Create binary documents, modify, and share them in one online editing solution that saves you time and improves your productivity. All you need to do is sign up an account at DocHub, which takes just a few minutes.
You will not need to become an editing multitasker with DocHub. Its feature set is sufficient for speedy papers editing, regardless of the format you need to revise. Begin with creating an account and see how easy document management might be with a tool designed particularly to suit your needs.
Genotyping single nucleotide polymorphisms, or SNPs, using TaqMan Assays has been very well established. But have you heard about copy number variations? Copy number variation (CNV) is a type of structural variation that occurs when a DNA segment of 1 kb to several megabases in length is present in variable copy numbers compared to a reference genome. These CNVs can influence gene expression and can be associated with specific phenotypes and diseases. This variation covers approximately 12% of the human genome and includes deletions and duplications. TaqMan Copy Number assays offer a targeted approach combining high accuracy, specificity, ease of use and sample throughput, to validate copy number changes or screen large sample sets. So how does this all work? Lets take a look at our lab book TaqMan Copy Number assays are a duplex experiment using a FAM labeled target assay and a VIC labeled reference assay in the same well to quantify small fold changes. The reference assay targets a