Think of sequencing as reading the book of your personal genetics—every base (T, C, G, and A) is read in order and saved for the future. Using a reference sequence (a model sequence to compare to), Helix can determine when a base in an individual is different and the specific position of that variation within your DNA.

Most consumer genetics companies use a process called genotyping to read DNA data. If sequencing is reading a book, then genotyping is like reading a few letters on a few pages. Yes, you can learn a thing or two, but you don’t get the full story. Because genotyping requires an analysis of a specific variation, each experiment has to be done one at a time. With sequencing, you’re capturing all the words on all the pages and can flip through anytime. 

Learn More => https://www.helix.com/support/about-helix

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