Strelka offers several features that make it a valuable tool in cancer genomics:
High Sensitivity: Capable of detecting low-frequency variants. Accuracy: Utilizes advanced algorithms to minimize false positives and false negatives. Scalability: Can handle large datasets, making it suitable for whole-genome and exome sequencing projects. Flexibility: Supports both somatic and germline variant calling. Compatibility: Integrates well with other bioinformatics tools and pipelines.
