Nebula Genomics Review | 30x Whole-Genomics Sequencing

Nebula Genomics is changing the world of DNA testing by offering whole-genome sequencing. Founded by George Church, professor of genetics at Harvard Medical School, Nebula Genomics‘ mission is to use whole genome sequencing to understand the causes of disease and develop gene therapies to eventually cure genetic diseases. Sequencing your DNA through Nebula Genomics will not only give you personal insight into your genetics, heritage and genetic dispositions but it will also contribute to the science of genetic testing/research.

Being a health science major myself and learning about Nebula Genomics and their mission, I was highly intrigued.

I wanted to purchase this particular kit because:

Heritage/family history: I know a little about where my ancestors came from, but there is still a lot to question.
Genetic disease predisposition: I don’t know very much about my dad’s side of the family (especially health concerns) but I do know that there are a few red flags. For example, my father recently had to have a lobe of his lung removed due to a small amount of cancer that was found. Being a non-smoker all his life but still developing lung cancer is a concern for me.
I wanted to try this kit myself so that in the future if my daughters wanted to find out more about their heritage/ancestry I could recommend the best possible DNA test for them. (Both of my daughters are adopted. Although both of their adoptions are open adoptions and they can learn about their family history through their birth mothers, there may still be questions they have that can’t be answered. This test will allow them to learn their full genetic history/predispositions.)

The Nebula Genomics 30x Whole-Genomics Sequencing Kit offers:

Whole genome sequencing decoding 100% of your DNA.
Privacy first DNA testing.
Nebula research library: new reports each week based on the latest scientific discoveries.
Genome exploration tools to answer any questions about your DNA.
Deep genetic ancestry: full Y chromosome and mitochondrial DNA sequencing and analysis.
Genomic big data access: FASTQ, BAM, and VCF files.
Data that can be used by physicians and genetic counselors.

So I recently purchased the 30x Whole-Genomics Sequencing kit.

I ordered my kit on February 10th. I received an email shortly afterwards that stated that due to COVID-19, I should anticipate shipping delays. However, after receiving an email that the package shipped on the 12th, it arrived to my home on the 13th! This was what was included in the kit that I received in the mail:

I was so excited when the kit arrived that I wanted to do it right then! So I registered the kit on the website and completed all of the surveys.

However, after I read the directions, I discovered that I couldn’t because they suggest not to have eaten or drank anything within a half hour of doing the test.

I waited until first thing in the morning and then completed the swab test. I was truly amazed by how easy this sequencing test was to do! All I had to do was rub two different swabs on the inside of my cheek for 60 seconds each and then use the vial that they sent me to transfer the sample from the swab into the liquid contained within the vial. Afterwards, I simply put the vial into a bag that came with the kit and then put it all within the pre-labeled envelope to send back for sequencing!

If you want to hear about my results please read my article, Biological Family | Genetics & Medical History! If you want to get started on your own Nebula Genomics kit now simply click here or on the banner below!