Software pipeline demonstrates accurate detection of somatic insertions and deletions in cancer genomes, highlighting scalable workflows for paired-end sequencing data.
cgpPindel is a modified version of Pindel that is optimized for detecting somatic insertions and deletions (indels) in cancer genomes and other samples compared to a reference control. Post-hoc filters remove false positive calls, resulting in a high-quality dataset for downstream analysis. This unit provides concise instructions for both a simple 'one-shot' execution of cgpPindel and a more detailed approach suitable for large-scale compute farms.
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Raine et al. (2015) studied this question.
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