返回
A graphical, interactive and GPU-enabled workflow to process long-read sequencing data
DOI:10.1186/s12864-021-07927-1.png)
摘要
En 中文
Background Long-read sequencing has great promise in enabling portable, rapid molecular-assisted cancer diagnoses. A key challenge in democratizing long-read sequencing technology in the biomedical and clinical community is the lack of graphical bioinformatics software tools which can efficiently process the raw nanopore reads, support graphical output and interactive visualizations for interpretations of results. Another obstacle is that high performance software tools for long-read sequencing data analyses often leverage graphics processing units (GPU), which is challenging and time-consuming to configure, especially on the cloud. Results We present a graphical cloud-enabled workflow for fast, interactive analysis of nanopore sequencing data using GPUs. Users customize parameters, monitor execution and visualize results through an accessible graphical interface. The workflow and its components are completely containerized to ensure reproducibility and facilitate installation of the GPU-enabled software. We also provide an Amazon Machine Image (AMI) with all software and drivers pre-installed for GPU computing on the cloud. Most importantly, we demonstrate the potential of applying our software tools to reduce the turnaround time of cancer diagnostics by generating blood cancer (NB4, K562, ME1, 238 MV4;11) cell line Nanopore data using the Flongle adapter. We observe a 29x speedup and a 93x reduction in costs for the rate-limiting basecalling step in the analysis of blood cancer cell line data. Conclusions Our interactive and efficient software tools will make analyses of Nanopore data using GPU and cloud computing accessible to biomedical and clinical scientists, thus facilitating the adoption of cost effective, fast, portable and real-time long-read sequencing.
Keyword:
Cancer diagnostics
Workflows
Cloud computing
Nanopore
GPU
FAIR
Long-read sequencing
Leukemia
AI总结
对已上传原文的论文进行重点信息的提取,主要内容包括:简要概述、研究摘要、背景介绍、关键亮点、图文解析、展望与总结。
期刊
IF:
3.7
论文数:
1.9W
被引数:
5.2W
机构
引用论文
Performance of neural network basecalling tools for Oxford Nanopore sequencing用于牛津纳米孔测序的神经网络基础调用工具的性能
GENOME BIOLOGY
IF9.4
DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing
SCIENTIFIC REPORTS
IF3.9
Guidelines for Validation of Next-Generation Sequencing-Based Oncology Panels A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists基于下一代测序的肿瘤学小组验证指南分子病理学协会和美国病理学家学院的联合共识建议
Molecular Testing Turnaround Time in Non-Small-Cell Lung Cancer: Monitoring a Moving Target
CLINICAL LUNG CANCER
IF3.3

