Unusual file formats within your day-to-day document management and editing operations can create immediate confusion over how to modify them. You may need more than pre-installed computer software for effective and speedy file editing. If you want to copy number in Amigaguide or make any other simple alternation in your file, choose a document editor that has the features for you to work with ease. To handle all the formats, including Amigaguide, opting for an editor that actually works well with all kinds of files is your best option.
Try DocHub for efficient file management, regardless of your document’s format. It has powerful online editing instruments that streamline your document management process. You can easily create, edit, annotate, and share any document, as all you need to access these features is an internet connection and an active DocHub account. Just one document tool is all you need. Do not lose time jumping between different applications for different files.
Enjoy the efficiency of working with an instrument designed specifically to streamline document processing. See how effortless it is to modify any file, even if it is the very first time you have dealt with its format. Register an account now and enhance your whole working process.
do you know that over two third of the entire Human Genome comprises of repetitive regions among this about 4 to 10 percent comprises of copy number variations which docHubly contributes to variation in the individuals of our population hello and welcome back to another interesting video of explore bio on genomic series I am Dr Abhishek and in this short video we will learn what a copy number variation is what are the causes of copy number variation how they can be identified and what are their consequences so without any delay lets begin copy number variation or cnv is one of the major causes of a structural variation in the genome in which the number of copies of a particular genome segment gets duplicated or deleted these copy number variations can technically range between thousand bases to 5 megabases but most cnvs are less than 10 KB long in this picture you can see individual 1 has 3 copies of genome segment highlighted in orange color in both the parental chromosomes due