DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing data

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.

Authors

Institutions

Publication Details

Journal
NAR Genomics and Bioinformatics
Published
2026-01-06
DOI
https://doi.org/10.1093/nargab/lqag021
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing data

van Overeem Hansen T, Ulrik Kristoffer Stoltze, Anna Byrjalsen, Christian M. Hagen et al.
NAR Genomics and Bioinformatics
Genomics and Rare Diseases
article

DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing data

van Overeem Hansen T, Ulrik Kristoffer Stoltze, Anna Byrjalsen, Christian M. Hagen, Karin Wadt, Henrik Hjalgrim, Simon Horskjær Rasmussen, Marie Bækvad-Hansen, Jonas Bybjerg-Grauholm, Mads Cort Nielsen, Kjeld Schmiegelow
article en

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.

NAR Genomics and BioinformaticsVol. 8(1)
Statens Serum Institut (DK), University of Copenhagen (DK), Novo Nordisk Foundation (DK), Rigshospitalet (DK), Danish Cancer Society (DK)
Børnecancerfonden, Novo Nordisk, Novo Nordisk Fonden
Openalex Percentile: Top 52%
Genomics and Rare Diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.