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Rates and patterns of chromosome evolution in enteric bacteria
Rates and patterns of chromosome evolution in enteric bacteria

... 1.3 Mb of unique DNA when compared to a very distantly related strain; by analyzing the genetic content and base composition of these strain-specific sequences, they concluded that nearly half of this DNA was gained through horizontal transfer. Considerable attention has been directed towards the in ...
Unit 5 quesitons
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... 8. Why do the purine and pyrimidine bases always pair together? 9. How are the two strands held together into the double helix? 10. Describe the Meselsohn-Stahl experiment. 11. What did this experiment prove? 12. What is the origin of replication? 13. Describe the replication fork. 14. What enzyme c ...
The Genome - OpenStax CNX
The Genome - OpenStax CNX

... The matched pairs of chromosomes in a diploid organism are called homologous chromosomes. Homologous chromosomes are the same length and have specic nucleotide segments called genes in exactly the same location, or locus. Genes, the functional units of chromosomes, determine specic characteristics ...
Genetic aspects of Multiple Sclerosis Boon, Maartje
Genetic aspects of Multiple Sclerosis Boon, Maartje

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INTRODUCTION TO BACTERIAL GENETICS
INTRODUCTION TO BACTERIAL GENETICS

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Homologous recombination

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Genomics for the Rancher: How Does it Work and What
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article here - Virus-X – A Horizon2020 project

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Epigenetics - UNM Biology

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Yeaman Commentary on Parchman et al 2013

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Blueprint of Life - The Bored of Studies Community
Blueprint of Life - The Bored of Studies Community

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Cellular Reproduction - Genomic DNA
Cellular Reproduction - Genomic DNA

... In eukaryotes, the genome consists of several double-stranded linear DNA molecules (Figure 2). Each species of eukaryotes has a characteristic number of chromosomes in the nuclei of its cells. cells have 46 chromosomes, while human ...
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Genomic library



A genomic library is a collection of the total genomic DNA from a single organism. The DNA is stored in a population of identical vectors, each containing a different insert of DNA. In order to construct a genomic library, the organism's DNA is extracted from cells and then digested with a restriction enzyme to cut the DNA into fragments of a specific size. The fragments are then inserted into the vector using DNA ligase. Next, the vector DNA can be taken up by a host organism - commonly a population of Escherichia coli or yeast - with each cell containing only one vector molecule. Using a host cell to carry the vector allows for easy amplification and retrieval of specific clones from the library for analysis.There are several kinds of vectors available with various insert capacities. Generally, libraries made from organisms with larger genomes require vectors featuring larger inserts, thereby fewer vector molecules are needed to make the library. Researchers can choose a vector also considering the ideal insert size to find a desired number of clones necessary for full genome coverage.Genomic libraries are commonly used for sequencing applications. They have played an important role in the whole genome sequencing of several organisms, including the human genome and several model organisms.
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