genomic library
71Bioinformatics — For the journal, see Bioinformatics (journal). Map of the human X chromosome (from the NCBI website). Assembly of the human genome is one of the greatest achievements of bioinformatics. Bioinformatics …
72Medical genetics — Clinical genetics redirects here. For the journal, see Clinical Genetics (journal). For a non technical introduction to the topic, see Introduction to Genetics. Part of a series on Genetics Key components Chromosome …
73Escherichia coli — E. coli redirects here. For the protozoan parasite, see Entamoeba coli. For the 2011 E.coli outbreak, see 2011 E. coli O104:H4 outbreak. For a specific strain, see Escherichia coli (disambiguation). For Escherichia coli in molecular biology, see… …
74Human genome — The human genome is the genome of Homo sapiens , which is stored on 23 chromosome pairs. Twenty two of these are autosomal chromosome pairs, while the remaining pair is sex determining. The haploid human genome occupies a total of just over 3… …
75David Pearce (philosopher) — For other people named David Pearce, see David Pearce (disambiguation). David Pearce Full name David Pearce Born United Kingdom …
76European Bioinformatics Institute — The European Bioinformatics Institute (EBI) is a centre for research and services in bioinformatics, and is part of European Molecular Biology Laboratory (EMBL). It is a pioneer of novel and developmental bioinformatics research. It has… …
77Gene — For a non technical introduction to the topic, see Introduction to genetics. For other uses, see Gene (disambiguation). This stylistic diagram shows a gene in relation to the double helix structure of DNA and to a chromosome (right). The… …
782 Base Encoding — The dream of human genome re sequencing within a reasonable time and cost (less than $1000) is becoming realized with recently developed next generation sequencing technologies. These technologies generate hundreds of thousands of small sequence… …
79Copy-number variation — This gene duplication has created a copy number variation. The chromosome now has two copies of this section of DNA, rather than one. Copy number variations (CNVs) a form of structural variation are alterations of the DNA of a genome that results …
80Massive parallel sequencing — is a term used to describe several revolutionary approaches to DNA sequencing, the so called next generation sequencing (NGS) technologies or second generation sequencing. These sequencing technologies have emerged in late 1996 [1][2] an have… …
