![]() ![]() A key aspect of research in genetics is associating sequence variations with heritable phenotypes. SNP is terminologically distinguished from mutation based on an arbitrary population frequency cutoff value: 1%, with SNP 1% and mutation 1%. SNP is the most common variation in the human genome and occurs approximately once every 100 to 300 bases. SNP, pronounced “snip,” stands for single-nucleotide polymorphism, which represents a substitution of one base for another, e.g., C to T or A to G. What are SNPs?įrom Bioinformatics - A Practical Approach by Shui Qing Ye, M.D., Ph.D. All of which using Flask, Kendo, and Python programming. This allows for everything from filtering to excel exporting. It creates a Responsive Grid of the user's specific genome. ![]() OS Genome's goal is to crawl various sources and give meaning to an individual's genome. OS Genome is an open source web application that allows users to gather the information they need to make sense of their own genome without needing to rely on outside services with unknown privacy policies. An Open Source Web Application for Genetic Data (SNPs) using 23AndMe and Data Crawling Technologies Description ![]()
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