FLEXIBLE, PRODUCTION-SCALE, HUMAN WHOLE GENOME SEQUENCING ON A BENCHTOP SEQUENCER
Kevin Green, Benjamin J. KrajacichiD, Kelly N. Wiseman, Peter T. Mains, Samantha RobertsoniD, Sophie Billings, Marina McCowin, Mitch SudkampiD, Ching Shing Lo, Bryan R. LajoieiD, Semyon KruglyakiD, Shawn LevyiD, Junhua ZhaoiD
Abstract
Human whole-genome sequencing (hWGS) provides comprehensive genomic information that can potentially help guide research in disease prevention and treatment and ultimately improve human health. Recent advancements in sequencing technology have improved sequencing quality and further reduced sequencing costs on bench-top sized instruments, making whole-genome sequencing an accessible technology for broader use. Here, we demonstrate the feasibility of a large whole genome sequencing project using a benchtop sequencer in a small laboratory setting, on a scale previously reserved for production-scale factory-sized machines. In this project, 807 samples were prepared and sequenced across 313 flow cells, with high sequencing quality at a median %Q30 of 96.6% and a median %Q40 of 89.31%. To screen library quality and maximize sample yield, we utilized 48-plex sample pre-pool QC runs to provide >1x coverage per sample prior to sample pooling and full-depth sequencing. With this strategy, we consistently achieved >30x human whole genome sequencing of three-plex sample trios with standard settings or up to 4 samples per run with a high-throughput run setting. Additionally, this low-pass data provided valuable sample-level insights, allowing for detection of chromosome copy number variations (CNV) prior to full-depth sequencing. With three instruments running concurrently, >2,800 30x human whole genomes could be sequenced per year. To further demonstrate additional flexibility present in the platform, we also explored two different use cases 1) large insert sizes (1kb+) library to achieve superior genome coverage; 2) a proof of concept for rapid WGS sequencing to minimize sample to answer turnaround time for time-critical sequencing applications. Sequencing of a 2x100 >30x human WGS can be achieved in <12 hours and subsequent generation of fastq, bam and vcf in <1 additional hour. This study provides a cost-effective and flexible real-world demonstration of achieving both high quality hWGS sequencing and instrument flexibility without the need for complex batching schemes or factory-sized sequencers.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- FWCI
- 0.30
- Field percentile
- 46th percentile
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Cost-efficient whole genome-sequencing using novel mostly natural sequencing-by-synthesis chemistry and open fluidics platform
Gilad Almogy, Mark Pratt, … Doron Lipson·bioRxiv·May 29, 2022
- Human Whole Genome Sequencing in South Africa
Brigitte Glanzmann, Tracey Jooste, … Craig John Kinnear·Scientific ReportsPeer-reviewed·Jan 12, 2021
- WxS-QC - a quality control pipeline for human Whole-Genome and Whole Exome sequencing cohorts
Gennadii A. Zakharov, Ruth Y. Eberhardt, … Vivek Iyer·BioinformaticsPeer-reviewed·Jul 1, 2026
- A new massively parallel nanoball sequencing platform for whole exome research
Yu Xu, Zhe Lin, … Qiang Gao·BMC BioinformaticsPeer-reviewed·Mar 25, 2019
- WHOLE GENOME BISULPHITE SEQUENCING USING THE ILLUMINA HISEQ X SYSTEM
Masako Suzuki, Will Liao, … John M. Greally·Genome ResearchPeer-reviewed·Sep 1, 2018
- SYSTEM ANALYSIS OF THE SEQUENCING QUALITY OF HUMAN WHOLE EXOME SAMPLES ON BGI NGS PLATFORM
Vera Belova, Anna S. Pavlova, … Dmitriy O. Korostin·Scientific ReportsPeer-reviewed·Jan 12, 2022