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Words near each other
・ Genomatix
・ Genome
・ Genome (book)
・ Genome (disambiguation)
・ Genome (novel)
・ Genome Biology
・ Genome browser
・ Genome Compiler
・ Genome diversity and karyotype evolution of mammals
・ Genome editing
・ Genome engineering
・ Genome evolution
・ Genome Hazard
・ Genome instability
・ Genome Institute of Singapore
Genome project
・ Genome Reference Consortium
・ Genome Research
・ Genome Research Foundation
・ Genome size
・ Genome survey sequence
・ Genome Therapeutics Corporation
・ Genome Valley
・ Genome-based peptide fingerprint scanning
・ Genome-wide association study
・ Genome@home
・ Genomes OnLine Database
・ Genomespace
・ Genomic and Medical Data
・ Genomic convergence


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Genome project : ウィキペディア英語版
Genome project

Genome projects are scientific endeavours that ultimately aim to determine the complete genome sequence of an organism (be it an animal, a plant, a fungus, a bacterium, an archaean, a protist or a virus) and to annotate protein-coding genes and other important genome-encoded features. The genome sequence of an organism includes the collective DNA sequences of each chromosome in the organism. For a bacterium containing a single chromosome, a genome project will aim to map the sequence of that chromosome. For the human species, whose genome includes 22 pairs of autosomes and 2 sex chromosomes, a complete genome sequence will involve 46 separate chromosome sequences.
The Human Genome Project was a landmark genome project that is already having a major impact on research across the life sciences, with potential for spurring numerous medical and commercial developments.〔
==Genome assembly==
(詳細はDNA sequences and putting them back together to create a representation of the original chromosomes from which the DNA originated. In a shotgun sequencing project, all the DNA from a source (usually a single organism, anything from a bacterium to a mammal) is first fractured into millions of small pieces. These pieces are then "read" by automated sequencing machines, which can read up to 1000 nucleotides or bases at a time. (The four bases are adenine, guanine, cytosine, and thymine, represented as AGCT.) A genome assembly algorithm works by taking all the pieces and aligning them to one another, and detecting all places where two of the short sequences, or ''reads'', overlap. These overlapping reads can be merged, and the process continues.
Genome assembly is a very difficult computational problem, made more difficult because many genomes contain large numbers of identical sequences, known as repeats. These repeats can be thousands of nucleotides long, and some occur in thousands of different locations, especially in the large genomes of plants and animals.
The resulting (draft) genome sequence is produced by combining the information sequenced contigs and then employing linking information to create scaffolds. Scaffolds are positioned along the physical map of the chromosomes creating a "golden path".
===Assembly software===
Originally, most large-scale DNA sequencing centers developed their own software for assembling the sequences that they produced. However, this has changed as the software has grown more complex and as the number of sequencing centers has increased. An example of such assembler ''Short Oligonucleotide Analysis Package'' developed by BGI for de novo assembly of human-sized genomes, alignment, SNP detection, resequencing, indel finding, and structural variation analysis.〔〔〔

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Genome project」の詳細全文を読む



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