Abstract
We present Butler, a computational tool that facilitates large-scale genomic analyses on public and academic clouds. Butler includes innovative anomaly detection and self-healing functions that improve the efficiency of data processing and analysis by 43% compared with current approaches. Butler enabled processing of a 725-terabyte cancer genome dataset from the Pan-Cancer Analysis of Whole Genomes (PCAWG) project in a time-efficient and uniform manner.
Originalsprog | Engelsk |
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Tidsskrift | Nature Biotechnology |
Vol/bind | 38 |
Udgave nummer | 3 |
Sider (fra-til) | 288-292 |
ISSN | 1087-0156 |
DOI | |
Status | Udgivet - mar. 2020 |