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Prostate cancer is a leading cause of cancer death in males throughout the world and has the largest estimated effect of heritability among the most common tumor types. Copy Number Variants (CNVs) are a recently recognized class of human germline polymorphisms (Iafrate AJ, et al. (2004) Nat Genet...

"Single nucleotide variant detection in multiple foci of three prostate cancer tumors"
"Copy number variant detection in multiple foci of three prostate cancer tumors"
"SNV detection from formalin fixed paraffin embedded (FFPE) samples"
"Usage of small amounts of DNA for Illumina sequencing"
"Background: Massively parallel sequencing technologies have brought an enormous increase in sequencing throughput. However, these technologies need to be further improved with regard to reproducibility and applicability to clinical samples and settings. Methods: Using identification of genetic var...
Data Access Committee EGAC00001000030
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