Abstract
(1) Background: Next-generation sequencing (NGS) of patients with advanced tumors is becoming an established method in Molecular Tumor Boards. However, somatic variant detection, interpretation, and report generation, require in-depth knowledge of both bioinformatics and oncology. (2) Methods: MIRACUM-Pipe combines many individual tools into a seamless workflow for comprehensive analyses and annotation of NGS data including quality control, alignment, variant calling, copy number variation estimation, evaluation of complex biomarkers, and RNA fusion detection. (3) Results: MIRACUM-Pipe offers an easy-to-use, one-prompt standardized solution to analyze NGS data, including quality control, variant calling, copy number estimation, annotation, visualization, and report generation. (4) Conclusions: MIRACUM-Pipe, a versatile pipeline for NGS, can be customized according to bioinformatics and clinical needs and to support clinical decision-making with visual processing and interactive reporting.
| Original language | English |
|---|---|
| Article number | 3456 |
| Journal | Cancers |
| Volume | 15 |
| Issue number | 13 |
| ISSN | 2072-6694 |
| DOIs | |
| Publication status | Published - 07.2023 |
Funding
| Funders | Funder number |
|---|---|
| MIRACUM | FKZ 01ZZ2015, 01ZZ1801A, 01ZZ1801B |
| Deutsche Forschungsgemeinschaft (DFG) | EXC 22167-390884018 |
| Bundesministerium für Bildung und Forschung | |
| Deutsche Krebshilfe | 70114112 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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SDG 6 Clean Water and Sanitation
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SDG 9 Industry, Innovation, and Infrastructure
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