ArticleNAR genomics and bioinformatics2026
DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing data.
Article in NAR genomics and bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Population screening for rare genetic diseases has the potential to increase early diagnosis and treatment, but the high cost of next-generation sequencing limits widespread implementation. Double-batched sequencing (DoBSeq) is a cost-effective method that uses two-dimensional overlapping pool sequencing to enable individual-level rare variant detection. However, the resulting high-depth, complex data require a specialized workflow for efficient, sensitive, and reproducible analysis. We developed DoBSeqWF (DoBSeq Workflow), a Nextflow-based pipeline that processes pooled sequencing data from alignment through variant calling, filtering, and final variant assignment. Using a childhood cancer cohort of 200 individuals with whole genome sequencing as a reference, we created training and validation datasets, benchmarked multiple variant callers, and implemented machine learning filters to improve rare variant detection while maintaining high sensitivity. DoBSeqWF demonstrates accurate and scalable rare variant detection within the evaluated experimental setting and provides a promising avenue for future cost-effective genetic screening programmes.
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