Copy number variations (CNVs) are a pervasive form of genomic variation that entail duplications or deletions of DNA segments ranging from kilobases to megabases. In animal genomes, CNVs contribute ...
Scientists at Barts and The London School of Medicine and Dentistry (Mark Caulfield, Graham Hitman, Philip Howard, Toby Johnson, Abiodun Onipinla and Patricia Munroe), who are part of the Wellcome ...
Gene Duplications Give Clues to Humanness: All told, the researchers found more than 4000 genes that showed lineage-specific changes in copy number, with the numbers steadily increasing over ...
A form of rare genomic structural variation called copy number variants (CNVs) may be more closely associated with schizophrenia than bipolar disorder. A new study published in Biological Psychiatry ...
Losses and duplications of whole chunks of DNA at sites across our genomes are likely to play a role in autism spectrum disorders, suggests a new study published in the journal Nature. The ...
Dr Aaron Wenger reveals how improvements in long-read sequencing technology is enabling the elucidation of complex disease ...
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