|
|
|
|
The 'Dark Matter' of Cancer Genomics: Revealing Undetected Structural Variants in Leukemia
This white paper is based on a webinar presentation by Dr. James Broach of the Penn State College of Medicine. He discussed methods for capturing a comprehensive snapshot of all variants — both point mutations and structural variants — present in a tumor sample in order to gain insights about the genetic and genomic basis of individual cancers. Download it from GenomeWeb’s White Paper Channel. |
|
|
Genetic Testing Improves Outcomes for Patients with Rare Inherited Retinal Diseases
In this whitepaper from Informed DNA learn how genetic testing can be vital to the diagnosis of rare inherited retinal diseases and syndromic conditions and is important in the management of all patients. Download it from GenomeWeb’s White Paper Channel. |
Δεν υπάρχουν σχόλια:
Δημοσίευση σχολίου