Copy number variation (CNV) refers to an increase or decrease in the number of copies of a DNA sequence in a genome, which can subsequently be implicit in promoting aberrant gene expression patterns ...
Many medically relevant genes reside in “dark regions” of the genome that have long been elusive. To address this, we developed Paraphase – a computational tool that accurately resolves and analyzes ...
NimbleGen has entered into a partnership with the Korea Centers for Disease Control and Prevention (KCDC) and Macrogen, Inc. to conduct an 8-month intensive Copy Number Variation (CNV) study of Korean ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback