Back to search

Article

Findings from Precision Oncology in the Clinic: Rare, Novel Variants are a Significant Contributor to Scaling Molecular Diagnostics

2021-05-19

Abstract excerpt

<title>Abstract</title> <p><bold><italic>Background</italic></bold><italic>: Next generation sequencing for oncology patient management is now routine in clinical pathology laboratories. Although wet lab, sequencing and pipeline tasks are largely automated, the analysis of variants for clinical reporting remains largely a manual task. The increasing volume of sequencing data and the limited availability of geneti...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
3788c0aa-efb0-5c89-89fd-0a6f55e12a39
DOI
10.21203/rs.3.rs-537063/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Findings from Precision Oncology in the Clinic: Rare, Novel Variants are a Significant Contributor to Scaling Molecular DiagnosticsDOI 10.21203/rs.3.rs-537063/v1
Select a neighboring publication to make it the new centre.