The complete set of DNA in an organism is called a genome. Almost every cell in the body contains a complete copy of about 3 billion base pairs of DNA, or letters, that make up the human genome. With its four-letter language, DNA contains the information necessary to build the human body. A gene traditionally refers to the area of ​​DNA that contains instructions for making a specific protein or set of proteins. Each of the 20,000 to 25,000 genes stimulated in the human genome codes for an average of three proteins. Genomics is essentially a combination of recombinant DNA, DNA sequencing and bioinformatics methods for sequencer, assembler and analyzer the structure and function of genomes. It differs from "classical genetics" in that it considers the complete complement of the hereditary material of an organism, rather than a gene or a gene product at the same time. In addition, genomics focuses on the interactions between loci and alleles within the genome and other interactions such as epistasis, pleiotropy and heterosis. Genomics takes advantage of the availability of complete DNA sequences for interiors. The organization was made possible both by the pioneer work of Fred Sanger and by the latest sequencing technology of the new generation.
Posters & Accepted Abstracts: Journal of Tissue Science and Engineering
Posters & Accepted Abstracts: Journal of Tissue Science and Engineering
Scientific Tracks Abstracts: Journal of Tissue Science and Engineering
Scientific Tracks Abstracts: Journal of Tissue Science and Engineering
Posters & Accepted Abstracts: Metabolomics:Open Access
Posters & Accepted Abstracts: Metabolomics:Open Access
Posters & Accepted Abstracts: Journal of Metabolic Syndrome
Posters & Accepted Abstracts: Journal of Metabolic Syndrome
Keynote: Metabolomics:Open Access
Keynote: Metabolomics:Open Access
Journal of Genetics and Genomes received 65 citations as per Google Scholar report
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