• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

DeF-GPU:利用GPU架构在乙型肝炎病毒基因组DNA中高效且有效地发现缺失

DeF-GPU: Efficient and effective deletions finding in hepatitis B viral genomic DNA using a GPU architecture.

作者信息

Cheng Chun-Pei, Lan Kuo-Lun, Liu Wen-Chun, Chang Ting-Tsung, Tseng Vincent S

机构信息

Department of Computer Science and Information Engineering, National Cheng Kung University, Tainan 701, Taiwan.

Department of Internal Medicine, National Cheng Kung University Medical College and Hospital, Tainan 701, Taiwan.

出版信息

Methods. 2016 Dec 1;111:56-63. doi: 10.1016/j.ymeth.2016.07.020. Epub 2016 Jul 30.

DOI:10.1016/j.ymeth.2016.07.020
PMID:27480381
Abstract

Hepatitis B viral (HBV) infection is strongly associated with an increased risk of liver diseases like cirrhosis or hepatocellular carcinoma (HCC). Many lines of evidence suggest that deletions occurring in HBV genomic DNA are highly associated with the activity of HBV via the interplay between aberrant viral proteins release and human immune system. Deletions finding on the HBV whole genome sequences is thus a very important issue though there exist underlying the challenges in mining such big and complex biological data. Although some next generation sequencing (NGS) tools are recently designed for identifying structural variations such as insertions or deletions, their validity is generally committed to human sequences study. This design may not be suitable for viruses due to different species. We propose a graphics processing unit (GPU)-based data mining method called DeF-GPU to efficiently and precisely identify HBV deletions from large NGS data, which generally contain millions of reads. To fit the single instruction multiple data instructions, sequencing reads are referred to as multiple data and the deletion finding procedure is referred to as a single instruction. We use Compute Unified Device Architecture (CUDA) to parallelize the procedures, and further validate DeF-GPU on 5 synthetic and 1 real datasets. Our results suggest that DeF-GPU outperforms the existing commonly-used method Pindel and is able to exactly identify the deletions of our ground truth in few seconds. The source code and other related materials are available at https://sourceforge.net/projects/defgpu/.

摘要

乙型肝炎病毒(HBV)感染与肝硬化或肝细胞癌(HCC)等肝脏疾病风险增加密切相关。许多证据表明,HBV基因组DNA中发生的缺失通过异常病毒蛋白释放与人体免疫系统之间的相互作用,与HBV的活性高度相关。因此,在HBV全基因组序列上发现缺失是一个非常重要的问题,尽管挖掘如此庞大而复杂的生物学数据存在挑战。尽管最近设计了一些新一代测序(NGS)工具来识别插入或缺失等结构变异,但其有效性通常局限于人类序列研究。由于物种不同,这种设计可能不适用于病毒。我们提出了一种基于图形处理单元(GPU)的数据挖掘方法DeF-GPU,以从通常包含数百万条读数的大型NGS数据中高效、精确地识别HBV缺失。为了适应单指令多数据指令,测序读数被视为多数据,缺失发现过程被视为单指令。我们使用统一计算设备架构(CUDA)对这些过程进行并行化,并在5个合成数据集和1个真实数据集上进一步验证了DeF-GPU。我们的结果表明,DeF-GPU优于现有的常用方法Pindel,并且能够在几秒钟内准确识别我们真实数据中的缺失。源代码和其他相关材料可在https://sourceforge.net/projects/defgpu/获取。

相似文献

1
DeF-GPU: Efficient and effective deletions finding in hepatitis B viral genomic DNA using a GPU architecture.DeF-GPU:利用GPU架构在乙型肝炎病毒基因组DNA中高效且有效地发现缺失
Methods. 2016 Dec 1;111:56-63. doi: 10.1016/j.ymeth.2016.07.020. Epub 2016 Jul 30.
2
Detecting exact breakpoints of deletions with diversity in hepatitis B viral genomic DNA from next-generation sequencing data.从下一代测序数据中检测乙型肝炎病毒基因组 DNA 多样性缺失的精确断点。
Methods. 2017 Oct 1;129:24-32. doi: 10.1016/j.ymeth.2017.08.005. Epub 2017 Aug 10.
3
Analysis of HBV Genomes Integrated into the Genomes of Human Hepatoma PLC/PRF/5 Cells by HBV Sequence Capture-Based Next-Generation Sequencing.基于 HBV 序列捕获的下一代测序分析整合到人肝癌 PLC/PRF/5 细胞基因组中的 HBV 基因组。
Genes (Basel). 2020 Jun 18;11(6):661. doi: 10.3390/genes11060661.
4
Hepatocellular carcinoma-associated single-nucleotide variants and deletions identified by the use of genome-wide high-throughput analysis of hepatitis B virus.通过乙型肝炎病毒全基因组高通量分析鉴定出的肝细胞癌相关单核苷酸变异和缺失
J Pathol. 2017 Oct;243(2):176-192. doi: 10.1002/path.4938. Epub 2017 Aug 17.
5
Single-Molecule Sequencing Reveals Complex Genome Variation of Hepatitis B Virus during 15 Years of Chronic Infection following Liver Transplantation.单分子测序揭示肝移植后慢性感染15年期间乙型肝炎病毒的复杂基因组变异
J Virol. 2016 Jul 27;90(16):7171-7183. doi: 10.1128/JVI.00243-16. Print 2016 Aug 15.
6
Clustering infection of hepatitis B virus genotype B4 among residents in Vietnam, and its genomic characters both intra- and extra-family.越南居民中B4型乙型肝炎病毒的聚集性感染及其家庭内和家庭外的基因组特征。
PLoS One. 2017 Jul 28;12(7):e0177248. doi: 10.1371/journal.pone.0177248. eCollection 2017.
7
Gene copy number variations in the leukocyte genome of hepatocellular carcinoma patients with integrated hepatitis B virus DNA.合并乙型肝炎病毒DNA的肝细胞癌患者白细胞基因组中的基因拷贝数变异
Oncotarget. 2016 Feb 16;7(7):8006-18. doi: 10.18632/oncotarget.6895.
8
A double-spliced defective hepatitis B virus genome derived from hepatocellular carcinoma tissue enhanced replication of full-length virus.源自肝细胞癌组织的双剪接缺陷型乙型肝炎病毒基因组增强了全长病毒的复制。
J Med Virol. 2009 Feb;81(2):230-7. doi: 10.1002/jmv.21393.
9
Next-generation sequencing revealed divergence in deletions of the preS region in the HBV genome between different HBV-related liver diseases.下一代测序技术揭示了不同乙型肝炎病毒相关肝病的乙型肝炎病毒基因组前 S 区缺失的差异。
J Gen Virol. 2017 Nov;98(11):2748-2758. doi: 10.1099/jgv.0.000942. Epub 2017 Oct 12.
10
Early MinION™ nanopore single-molecule sequencing technology enables the characterization of hepatitis B virus genetic complexity in clinical samples.早期 MinION™ 纳米孔单分子测序技术可用于临床样本中乙型肝炎病毒遗传复杂性的特征分析。
PLoS One. 2018 Mar 22;13(3):e0194366. doi: 10.1371/journal.pone.0194366. eCollection 2018.

引用本文的文献

1
Applications of next-generation sequencing analysis for the detection of hepatocellular carcinoma-associated hepatitis B virus mutations.下一代测序分析在检测与肝细胞癌相关的乙型肝炎病毒突变中的应用。
J Biomed Sci. 2018 Jun 2;25(1):51. doi: 10.1186/s12929-018-0442-4.