Ontology highlight
ABSTRACT:
PROVIDER: EGAC00001000030 | EGA |
REPOSITORIES: EGA
BMC medical genomics 20110929
<h4>Background</h4>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.<h4>Methods</h4>Using identification of genetic variations in prostate cancer as an example we address three crucial challenges in the field of targeted re-sequencing: Small nucleotide variation (SNV) detection in samples of formalin-fixed ...[more]