HIVID2: an accurate tool to detect virus integrations in the host genome

计算机科学 基因组 寄主(生物学) 数据集成 计算生物学 生物 任务(项目管理) 数据挖掘 基因 遗传学 管理 经济
作者
Xi Zeng,Linghao Zhao,Chenhang Shen,Yi Zhou,Guoliang Li,Wing‐Kin Sung
出处
期刊:Bioinformatics [Oxford University Press]
卷期号:37 (13): 1821-1827 被引量:6
标识
DOI:10.1093/bioinformatics/btab031
摘要

Virus integration in the host genome is frequently reported to be closely associated with many human diseases, and the detection of virus integration is a critically challenging task. However, most existing tools show limited specificity and sensitivity. Therefore, the objective of this study is to develop a method for accurate detection of virus integration into host genomes.Herein, we report a novel method termed HIVID2 that is a significant upgrade of HIVID. HIVID2 performs a paired-end combination (PE-combination) for potentially integrated reads. The resulting sequences are then remapped onto the reference genomes, and both split and discordant chimeric reads are used to identify accurate integration breakpoints with high confidence. HIVID2 represents a great improvement in specificity and sensitivity, and predicts breakpoints closer to the real integrations, compared with existing methods. The advantage of our method was demonstrated using both simulated and real datasets. HIVID2 uncovered novel integration breakpoints in well-known cervical cancer-related genes, including FHIT and LRP1B, which was verified using protein expression data. In addition, HIVID2 allows the user to decide whether to automatically perform advanced analysis using the identified virus integrations. By analyzing the simulated data and real data tests, we demonstrated that HIVID2 is not only more accurate than HIVID but also better than other existing programs with respect to both sensitivity and specificity. We believe that HIVID2 will help in enhancing future research associated with virus integration.HIVID2 can be accessed at https://github.com/zengxi-hada/HIVID2/.Supplementary data are available at Bioinformatics online.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
ls完成签到,获得积分10
4秒前
Hello应助甘楽采纳,获得10
4秒前
DrWang完成签到,获得积分10
4秒前
Solar energy完成签到,获得积分10
5秒前
5秒前
6秒前
思源应助清晨牛采纳,获得10
6秒前
大模型应助Mr.Left采纳,获得10
7秒前
LLY完成签到,获得积分10
7秒前
10秒前
朗源Wu给朗源Wu的求助进行了留言
11秒前
shuyi完成签到 ,获得积分10
12秒前
科研通AI5应助飞翔的翅膀采纳,获得10
14秒前
00发布了新的文献求助10
17秒前
yj完成签到,获得积分10
19秒前
充电宝应助朝闻道采纳,获得10
20秒前
苏夏完成签到 ,获得积分10
20秒前
有魅力强炫完成签到,获得积分10
22秒前
23秒前
JWKim完成签到,获得积分10
24秒前
00完成签到,获得积分10
25秒前
26秒前
mojito完成签到 ,获得积分10
28秒前
32秒前
33秒前
科研通AI2S应助科研通管家采纳,获得10
35秒前
ldh032应助科研通管家采纳,获得10
35秒前
Rye227应助科研通管家采纳,获得20
35秒前
35秒前
榕树完成签到,获得积分10
38秒前
TYTY发布了新的文献求助10
38秒前
Yolo发布了新的文献求助10
39秒前
40秒前
shenmizhe完成签到,获得积分10
41秒前
42秒前
道衍先一完成签到,获得积分10
42秒前
lihai1完成签到,获得积分10
45秒前
45秒前
朗源Wu完成签到,获得积分10
46秒前
黑猫完成签到,获得积分10
47秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Technologies supporting mass customization of apparel: A pilot project 450
Mixing the elements of mass customisation 360
Периодизация спортивной тренировки. Общая теория и её практическое применение 310
the MD Anderson Surgical Oncology Manual, Seventh Edition 300
Nucleophilic substitution in azasydnone-modified dinitroanisoles 300
Political Ideologies Their Origins and Impact 13th Edition 260
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3781487
求助须知:如何正确求助?哪些是违规求助? 3327136
关于积分的说明 10229537
捐赠科研通 3041969
什么是DOI,文献DOI怎么找? 1669742
邀请新用户注册赠送积分活动 799258
科研通“疑难数据库(出版商)”最低求助积分说明 758757