Examples of 'copy number variation' in a sentence
Meaning of "copy number variation"
copy number variation: This phrase is a term used in genetics to describe differences in the number of copies of a particular gene or DNA sequence in the genome
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- The variation of the number of copies (normally two) of a gene, or of sequences of DNA, in the genome of a specific individual; has been linked to some diseases
How to use "copy number variation" in a sentence
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copy number variation
Systems and methods to detect copy number variation.
Copy number variation found to cause rare kidney disease.
In some cases a level categorized as a copy number variation is adjusted.
The effect of copy number variation in FcYRIIc is also especially interesting.
Methods to detect rare mutations and copy number variation.
Detennining copy number variation based on the quantitative measure of families in the sets.
Diet and the evolution of human gene copy number variation.
Determining copy number variation based on the quantitative measure of families in each set.
Sequence data is assembled and analyzed for copy number variation.
In certain cases the absence of a copy number variation is determined by a categorization module.
Systems and methods to detect rare mutations and copy number variation.
It can also contribute to the copy number variation seen in some gene clusters.
In contrast FcYRIIa and FcyRllb do not show gene copy number variation.
In some methods copy number variation is detected using competitive genomic hybridization arrays.
This could interfere with detecting copy number variation in a sample.
See also
Copy number variation is a very important type of structural variation and has been studied extensively.
Origins and functional impact of copy number variation in the human genome.
This prevents embryos from being labeled as mosaic based solely on copy number variation.
The extent to which copy number variation contributes to human disease is not yet known.
A range sometimes can define an expected range or expected level range for a copy number variation.
Research on the relationship between copy number variation and disease has a long history.
Copy number variation and association studies Copy number variation and association studies.
In another embodiment the method further comprises determining copy number variation between the sets.
DNA copy number variation.
Often a PAV is determined for a specific copy number variation.
RNA copy number variation.
A report is generated, mapping genome positions and copy number variation.
Copy number variation determination, methods and systems.
A novel genomic approach to studying DNA copy number variation in schizophrenia and bipolar disorder.
Copy number variation ( cnv ) is the most prevalent structural changes in the human genome.
In instances, reads may be sequences unrelated to copy number variation analysis.
As shown herein, copy number variation detection methods can be implemented as follows.
A method for providing a statistical likelihood of a fetal copy number variation comprising,.
Figure 5 illustrates exemplary copy number variation results performed using a microfluidic device.
Copy number variation ( cnv ) calling and association analyses were performed using penncnv software.
The blocking of repetitive sequence hybridization allows detection of so-called " unique sequence " copy number variation.
Often, a fetal copy number variation is a copy number variation in the genome of a fetus.
Reports are generated, mapping genome positions and copy number variation show in Fig.
Copy number variation of the SELENBP1 gene in schizophrenia.
One of the more interesting types of genetic alteration is copy number variation (CNV).
Copy number variation ( CNV ) is an important cause of neuropsychiatric disorders.
Some basics notions about genetic and more specifically about copy number variation ( CNV ).
FIG . 4A is graphical copy number variation detection report generated from a normal, non cancerous subject.
Is a diagram, 200 showing a strategy for detection of copy number variation in paired subject.
RCCX is a copy number variation ( CNV ) gene cluster located on chromosome 6.
This is a mutation called a copy number variation ( CNV ).
Key words, genome rearrangement, cancer, next-generation sequencing, copy number variation.
FIG . 1 shows a method of determining copy number variation ( CNV ).
As shown in FIGURE 28, embodiments effectively quantify targets in a copy number variation ( CNV ) assay.
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