Add to ORKGare changes in the number of copies of DNA in specific regions of the genome, and can vary in size from 1 kb to a complete chromosome arm [14]. CNAs have been linked to many different types of disease, such as cancer, HIV acquisition and progression, autoimmune diseases, and Alzheimer and Parkinson’
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Se adjunta un fichero pdf con los datos de investigación titulado "Supplementary Material for \Detec...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
Abstract Background Alterations in the number of copies of genomic DNA that are common or recurrent ...
DNA copy number variations are now recognized as an impor-tant contributor to human genetic disease....
Copy number changes, the gains and losses of chromosome segments, are a common type of genetic varia...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
Copy number variation (CNV) in genomic DNA is linked to a variety of human diseases (including c...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Se adjunta un fichero pdf con los datos de investigación titulado "Supplementary Material for \Detec...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
Abstract Background Alterations in the number of copies of genomic DNA that are common or recurrent ...
DNA copy number variations are now recognized as an impor-tant contributor to human genetic disease....
Copy number changes, the gains and losses of chromosome segments, are a common type of genetic varia...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
To further explore the extent of structural large-scale variation in the human genome, we assessed c...
Copy number variation (CNV) in genomic DNA is linked to a variety of human diseases (including c...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Accurate genotyping of sequence variation in repeated and copy number variable regions of genomes re...
Se adjunta un fichero pdf con los datos de investigación titulado "Supplementary Material for \Detec...