Genome sequencing service 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 service should not be confused with DNA profiling

This 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. The genome sequence of a single cell selected from a mixed population of cells can be determined using techniques of single cell genome sequencing service. This has important advantages in environmental microbiology in cases where a single cell of a particular microorganism species can be isolated from a mixed population by microscopy on the basis of its morphological or other distinguishing characteristics. In such cases the normally necessary steps of isolation and growth of the organism in culture may be omitted, thus allowing the sequencing of a much greater spectrum of organism genomes.

The process of genome sequencing service implies sequencing all of an organism's

Chromosomal DNA

Genome sequencing service of a single cell is selected from a large number of cells and can be determined using single cell genome sequencing techniques. It plays an important role in environmental microbiology particularly where a single cell of a specific microorganism species is identified from a mixed population on the basis of its morphological or other characteristics. In such cases, the necessary isolation steps of the organism in culture may be omitted. Thus, it enables the sequencing of organism genomes.

Role of Genome Sequencing service Companies in Medical Research

The technology of genome sequencing has now come to a point where it has become much more viable, affordable, precise and faster than before, allowing simultaneous identification and coding of samples. It has revolutionized the area of research in molecular biology, biochemistry, clinical diagnostics, pharmaceuticals as well as sample processing. Whole genome sequencing service has now become a part of holistic patient health-care and is being increasingly used as preventive medicine. The clinical industry is making extensive use of sequencing data for accurate interpretation of vague reports and samples with genetic predispositions of diseases. With a rising demand of whole genome sequencing a number of bioinformatics companies have recently cropped up to cater to the demands of clinical data interpretation and sample processing for research projects.

Author's Bio: 

CD Genomics was established in 2004, They aim at providing the research community with high quality Next Generation Sequencing, high throughput microarray services. Due to the demand for their services being increased; CD Genomics has already updated its technology platform to mainstream NGS and microarray instruments. Through nearly ten year's hard working and depend on their professional work team, they are proud of satisfying the needs of their clients both at home and abroad, which across more than 50 countries and districts. They always devote themselves to providing clients with the best and professional service. Contact now for Genome sequencing service.