Biology 1201A Lecture Notes - Lecture 5: Genome Canada, Genomics, Non-Coding Rna

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Genomics is the characterization of whole genomes, including their structures (sequences), functions, and evolution. Having the complete sequence of a genome makes it possible to study the complete set of genes in an organism or a virus, as well as other important sequences of their genomes. Having the complete sequence of a genome enables researchers to study the organization of genes in the genome as a whole and to determine how genes function together in networks. The complete sequencing of the approximately 3-billion-base-pair human genome the. The task was completed in 2003 by an international consortium of researchers and by a private company, celera genomics (headed by j. craig venter) Genomics consists of three main areas of study: 1. Genome sequence determination and annotation, which means obtaining the sequences of complete genomes and analyzing them to locate putative protein- coding and noncoding rna genes and other functionally important sequences in the genome: 2.

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