When your everyday tasks scope consists of a lot of document editing, you already know that every file format needs its own approach and in some cases specific software. Handling a seemingly simple LOG file can often grind the entire process to a stop, especially when you are trying to edit with inadequate tools. To prevent this kind of difficulties, get an editor that can cover all of your requirements regardless of the file format and copy number in LOG without roadblocks.
With DocHub, you will work with an editing multitool for any situation or file type. Minimize the time you used to spend navigating your old software’s functionality and learn from our intuitive interface as you do the work. DocHub is a efficient online editing platform that covers all of your file processing requirements for virtually any file, including LOG. Open it and go straight to efficiency; no prior training or reading instructions is required to enjoy the benefits DocHub brings to document management processing. Start by taking a couple of minutes to register your account now.
See improvements within your document processing immediately after you open your DocHub account. Save time on editing with our single solution that will help you be more productive 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