Examples of 'exome' in a sentence
Meaning of "exome"
Exome is the part of the genome formed by exons, which are the coding regions of genes. It represents the subset of an individual's genetic material that is translated into protein
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- The complete exon content of an organism or individual; the subset of the genome that excludes introns.
How to use "exome" in a sentence
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exome
Whole exome sequencing is the method of studying exome.
Diagnosis is typically done using full genome or exome sequencing.
Whole exome sequencing identifies cause of metabolic disease.
Comprehensive profile of all mutations present in the exome.
This is the difference between exome and transcriptome.
All the exons together are called the exome.
Transcriptome differs from exome of an organism.
Whole exome sequencing during pregnancy is complex data analysis.
The mutations were discovered using exome sequencing.
Exome sequencing was performed on two pools of samples to optimize the results.
Great flexibility based on the sequencing of the complete exome.
The researchers focused on the exome and the transcriptome.
The cases of exome sequencing solving medical mysteries are mounting fast.
This is detectable by exome sequencing.
The sum of all coding regions in a genome is called the exome.
See also
We sequenced the exome of one patient with infantile onset hypertrophic cardiomyopathy.
Arrows indicate mutated components identified by the whole exome sequencing.
The exome is part of the genome that express its information into proteins.
The untranslated regions of the genome are not included in exome sequencing.
Exome sequencing is a influential method to selectively sequence the coding regions of the genome.
It seems that in these cases the gain of exome sequencing outweighs its cost.
The target área for capture is likely to be different and smaller than the exome.
However genome wide and exome studies have revealed other genes related to crc.
The gene variant was identified using genetic linkage studies and whole exome sequencing.
Deletions and duplications in the exome can help pinpoint cause of unexplained genetic diseases.
Made neurophysiological diagnosis, through genetic sequencing to make exome.
The samples were then processed through the exome enrichment pulldown process and sequenced.
Whole exome sequencing has been used to identify most people with WSS.
We also analysed genetic mutations by exome sequencing in NMO patients in Southern Finland.
In exome sequencing, the mRNA is sequenced.
The researchers then compared the exome sequences between parents and their affected child.
Exome sequencing is sequencing the protein-encoding parts of the genome.
In certain embodiments, the entire exome or a subset thereof is isolated.
The whole exome sequencing can be achieved by introducing the step 7.
The collection of these coding sequences ( exons ) is known as exome of an organism.
DNA testing known as whole exome testing can identify a diagnosis and treatment for rare diseases.
The summary characteristics of the 22 cancers used for exome sequencing are listed.
Beyond all suspicion, exome sequencing in newborns with a suspected disorder.
We particularly recommend the sequencing of the complete exome for patients with,.
Importantly, whole genome and whole exome sequencing are useful for initial mutation discovery.
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability, an exome sequencing study.
Generally, using exome sequencing alone is not efficient enough to elucidate these types of conditions.
Figure 42 shows an exemplary scheme of exome phasing using the SNPs between the exons.
We generated exome data from 30 brazilian trios where the children were diagnosed with sporadic adhd.
Rare variants are increasingly being studied, as a consequence of exome and whole genome sequencing efforts.
These protein-coding regions of DNA are known collectively as the exome.
Informally, you can think of the exome as the DNA sequence of your genes.
I would like to send out for Robbie 's full exome panel.
In that case, Whole Exome Sequencing is necessary.
NGLY1 deficiency is difficult to diagnose, and most individuals have been identified by exome sequencing.
