Bancroft demonstrates over 6x improvement in genomic compression in applications, highlighting memory capacity and accelerator efficiency.
This paper presents Bancroft, a computational genomics acceleration platform that provides the illusion of practically infinite on-device memory capacity by compressing genomic data movement over PCIe. Bancroft introduces novel optimizations for efficient accelerator implementation to reference-based genome compression, including fixed-stride matching using cuckoo hashes and grouped header encoding, incorporated into a familiar interface supporting random accesses. We evaluate a prototype implementation of Bancroft on an affordable Alveo U50 FPGA equipped with 8 GB of HBM. Thanks to the orders of magnitude improvements in performance and resource efficiency of genomic compression, our prototype provides access to TBs of host-side genomic data at memory-class performance, measuring speeds over 30% of the on-device HBM bandwidth, an order of magnitude higher than conventional PCIe-limited architectures. Using a real-world pre-alignment filtering application, Bancroft demonstrates over 6x improvement over the conventional PCIe-attached architecture, achieving 30% of peak internal throughput of an accelerator with HBM, and 90% of the one with DDR4. Bancroft supports memory-class performance to practically infinite data capacity, using a small, fixed amount of HBM, making it an attractive solution to continued future scalability of computational genomics.
No takes yet. Share an insight, caveat, or question.
Lim et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: