When your everyday tasks scope consists of a lot of document editing, you know that every document format requires its own approach and often particular software. Handling a seemingly simple ANS file can often grind the whole process to a stop, especially when you are attempting to edit with inadequate software. To prevent this kind of difficulties, get an editor that will cover your needs regardless of the file format and copy number in ANS without roadblocks.
With DocHub, you will work with an editing multitool for any occasion or document type. Minimize the time you used to spend navigating your old software’s features and learn from our intuitive interface as you do the work. DocHub is a efficient online editing platform that covers all of your document processing needs for virtually any file, such as ANS. Open it and go straight to productivity; no prior training or reading instructions is required to enjoy the benefits DocHub brings to papers management processing. Begin with taking a few minutes to register your account now.
See upgrades within your papers processing just after you open your DocHub account. Save your time on editing with our single platform that will help you become more efficient with any document format with which you have to work.
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