Add to ORKGPosters: Genome Structure, Variation and Function: abstract no. 552TStructural variation has been recognized as a genetic risk factor contributing to human diseases, and in particular, congenital disorders. Smaller scale copy number variations (CNVs) have also been linked to a number of neurodevelopmental phenotypes, including intellectual disability as well as autism spectrum disorders. The precise detection of CNVs is therefore necessary for ...postprin
Despite considerable excitement over the potential functional significance of copy-number variants (...
Copy number variants affect both disease and normal phenotypic variation, but those lying within hea...
BACKGROUND:Understanding the genetic contribution to phenotype variation of human groups is necessar...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
Accurate and efficient genome-wide detection of copy number variants (CNVs) is essential for underst...
Copy number variation (CNV) is a class of genetic variation where large segments of the genome vary ...
Structural variations of DNA greater than 1 kilobase in size account for most bases that vary among ...
Copy number variation (CNV) has recently gained considerable interest as a source of genetic variati...
Copy number variants (CNVs) are suggested to have a widespread impact on the human genome and phenot...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Despite considerable excitement over the potential functional significance of copy-number variants (...
The detection of copy number variants (CNV) by array-based platforms provides valuable insight into ...
In the human genome, DNA variants give rise to a variety of complex phenotypes. Ranging from single ...
In the human genome, DNA variants give rise to a variety of complex phenotypes. Ranging from single ...
Copy number variants (CNVs) contribute to human genetic and phenotypic diversity. However, the distr...
Despite considerable excitement over the potential functional significance of copy-number variants (...
Copy number variants affect both disease and normal phenotypic variation, but those lying within hea...
BACKGROUND:Understanding the genetic contribution to phenotype variation of human groups is necessar...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
Accurate and efficient genome-wide detection of copy number variants (CNVs) is essential for underst...
Copy number variation (CNV) is a class of genetic variation where large segments of the genome vary ...
Structural variations of DNA greater than 1 kilobase in size account for most bases that vary among ...
Copy number variation (CNV) has recently gained considerable interest as a source of genetic variati...
Copy number variants (CNVs) are suggested to have a widespread impact on the human genome and phenot...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Despite considerable excitement over the potential functional significance of copy-number variants (...
The detection of copy number variants (CNV) by array-based platforms provides valuable insight into ...
In the human genome, DNA variants give rise to a variety of complex phenotypes. Ranging from single ...
In the human genome, DNA variants give rise to a variety of complex phenotypes. Ranging from single ...
Copy number variants (CNVs) contribute to human genetic and phenotypic diversity. However, the distr...
Despite considerable excitement over the potential functional significance of copy-number variants (...
Copy number variants affect both disease and normal phenotypic variation, but those lying within hea...
BACKGROUND:Understanding the genetic contribution to phenotype variation of human groups is necessar...