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Genome chips are miniaturized plates containing hundreds of microscopic wells on their surface. These wells contain DNA probes. DNA probes are basically stretches of cDNA from a particular genome.
When genomic DNA isolated from an organism is allowed to interact with the cDNA probes, come probes bind to the genomic DNA while others do not (depending on complementarity.
A laser light is used to read each well and look at what sequences are bound. This information is valuable to scientists who can determine changes in gene expression based on the information obtained from a gene chip
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What is a map of the distribution of cloned genomic DNA from genomic clone libraries?
A map of the distribution of cloned genomic DNA from genomic clone libraries shows the physical location of different DNA fragments within the genome. This type of map is used to study genetic organization, identify genes, and analyze specific regions of interest within the genome. It helps researchers understand the genomic structure and function of an organism.
How much percentage of genomic DNA is active?
kk
What is genomic region?
A genomic region refers to a specific part of a genome that may contain one or more genes along with regulatory elements. It can vary in size and is typically defined by its unique DNA sequence. Researchers often study genomic regions to understand their functions and the genetic variations present within them.
How does genomic information affect members of minority communities?
Genomic information can impact members of minority communities by contributing to the understanding and treatment of genetic diseases that disproportionately affect these groups. However, there are concerns about privacy, discrimination, and access to healthcare based on genomic data. It is important to address ethical and social implications to ensure equitable benefits and protections for all communities.
What is a genomic location?
A genomic location refers to a specific position or region on a chromosome where a particular gene, DNA sequence, or genetic marker is found. It is typically described using coordinate systems, such as base pair positions, which indicate the precise spot on the DNA strand. Understanding genomic locations is crucial for studying gene function, genetic variations, and their associations with diseases.
When was Genomic Standards Consortium created?
Genomic Standards Consortium was created in 2005.
When was Genomic Medicine Institute created?
Genomic Medicine Institute was created in 2005.
A collection of cloned recombinant plasmids that includes fragments from the entire genome of a cell is called a?
Genomic library
What is a map of the distribution of cloned genomic DNA from genomic clone libraries?
A map of the distribution of cloned genomic DNA from genomic clone libraries shows the physical location of different DNA fragments within the genome. This type of map is used to study genetic organization, identify genes, and analyze specific regions of interest within the genome. It helps researchers understand the genomic structure and function of an organism.
What do you mean by genomic in situ hybridisation technique?
Genomic In Situ Hybridization refers to use of total genomic DNA from one species as a probe for in situ hybridization to identify chromosomes, chromosome segments, or whole genomes originating from that species in a hybrid or backcross.
What is the TIGR database?
The Institute for Genomic Research
Where does genomic DNA present in a tissue?
In the mitochondria
What is use of Genomic library?
cloned genes -sarahhh(:
How much percentage of genomic DNA is active?
kk
What has the author Eric Engel written?
Eric Engel has written: 'Genomic imprinting and uniparental disomy in medicine' -- subject(s): Chromosome abnormalities, Genetic disorders, Genomic imprinting
What is genomic region?
A genomic region refers to a specific part of a genome that may contain one or more genes along with regulatory elements. It can vary in size and is typically defined by its unique DNA sequence. Researchers often study genomic regions to understand their functions and the genetic variations present within them.
What is the relationship between methylation and genomic imprinting?
Methylation is a process where methyl groups are added to DNA, which can affect gene expression. Genomic imprinting is a phenomenon where certain genes are expressed based on whether they are inherited from the mother or father. Methylation plays a key role in genomic imprinting by regulating which parent's gene is expressed.
