Whole genome sequencing (WGS) should not be confused with DNA profiling, by Torsten Kunert







Whole genome sequencing (also known as full genome sequencing, complete genome sequencing, or entire genome sequencing) is a laboratory process that determines the complete DNA sequence of an organism’s genome at a single time. This entails sequencing all of an organism’s chromosomal DNA as well as DNA contained in the mitochondria and, for plants, in the chloroplast.

Whole genome sequencing should not be confused with DNA profiling, which only determines the likelihood that genetic material came from a particular individual or group, and does not contain additional information on genetic relationships, origin or susceptibility to specific diseases. Also unlike full genome sequencing, SNP genotyping covers less than 0.1% of the genome. Almost all truly complete genomes are of microbes; the term “full genome” is thus sometimes used loosely to mean “greater than 95%”. The remainder of this article focuses on nearly complete human genomes.
We offer high-throughput genome sequencing technologies and are building Health Apps for the Natural Health Market.

We work with overseas institutes and clinics, primarily focusing on Alternative medicine, researching new ways to combat cancer.
Please contact Torsten Kunert USA +480-393-6318.
WGS is offered at $5,000 through our overseas partners.

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