Demo Data from EDBT 2026 / reviewers in the wild / expert
Johnny Le
dblp:238/2101
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2019
—ORCID · unresolved
Domains — the database's venue-derived domains; a paper can count in several
Systems, architecture and hardware · 1
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Computer architecture, parallel and distributed computing, and storage systems
1 paper |
Reconfigurable computing and FPGAs · 50% Cloud and datacenter computing · 50% | |
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Cloud and datacenter computing › cloud deployment
cloud FPGA deployment |
0.4 | 1 | 2019 | FPGA Accelerated INDEL Realignment in the Cloud · HPCA 2019 |
Reconfigurable computing and FPGAs
FPGA accelerator |
0.4 | 1 | 2019 | FPGA Accelerated INDEL Realignment in the Cloud · HPCA 2019 |
Bioinformatics and computational biology › sequence analysis
genomic sequence analysis |
0.1 | 1 | 2019 | FPGA Accelerated INDEL Realignment in the Cloud · HPCA 2019 |
Methods — techniques the papers use, named apart from their topics
hardware-software co-design · 0.8FPGA-as-a-service · 0.8
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2019 | FPGA Accelerated INDEL Realignment in the CloudabstractThe amount of data being generated in genomics is predicted to be between 2 and 40 exabytes per year for the next decade, making genomic analysis the new frontier and the new challenge for precision medicine. This paper explores targeted deployment of hardware accelerators in the cloud to improve the runtime and throughput of immensescale genomic data analyses. In particular, INDEL (INsertion/DELetion) realignment is a critical operation that enables diagnostic testings of cancer through error correction prior to variant calling. It is the slowest part of the somatic (cancer) genomic analysis pipeline, the alignment refinement pipeline, and represents roughly one-third of the execution time of timesensitive diagnostics for acute cancer patients. To accelerate genomic analysis, this paper describes a hardware accelerator for INDEL realignment (IR), and a hardware-software framework leveraging FPGAs-as-a-service in the cloud. We chose to implement genomics analytics on FPGAs because genomic algorithms are still rapidly evolving (e.g. the de facto standard “GATK Best Practices” has had five releases since January of this year). We chose to deploy genomics accelerators in the cloud to reduce capital expenditure and to provide a more quantitative performance and cost analysis. We built and deployed a sea of IR accelerators using our hardware-software accelerator development framework on AWS EC2 F1 instances. We show that our IR accelerator system performed 81× better than multi-threaded genomic analysis software while being 32× more cost efficient. Lisa Wu Wills, David Bruns-Smith, Frank A. Nothaft, Qijing Huang 0001, Sagar Karandikar, Johnny Le, Andrew Lin, Howard Mao, Brendan Sweeney, Krste Asanovic, David A. Patterson 0001, Anthony D. Joseph |
HPCA | 6 |