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PWN:扭曲网络上的增强随机游走用于疾病靶点优先级排序。

PWN: enhanced random walk on a warped network for disease target prioritization.

机构信息

Standigm Inc., 70, Nonhyeon-ro 85-gil, Gangnam-gu, Seoul, 06234, Republic of Korea.

Standigm UK Co., Ltd, 50-60 Station Road, Cambridge, CB1 2JH, UK.

出版信息

BMC Bioinformatics. 2023 Mar 21;24(1):105. doi: 10.1186/s12859-023-05227-x.

DOI:10.1186/s12859-023-05227-x
PMID:36944912
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10031933/
Abstract

BACKGROUND

Extracting meaningful information from unbiased high-throughput data has been a challenge in diverse areas. Specifically, in the early stages of drug discovery, a considerable amount of data was generated to understand disease biology when identifying disease targets. Several random walk-based approaches have been applied to solve this problem, but they still have limitations. Therefore, we suggest a new method that enhances the effectiveness of high-throughput data analysis with random walks.

RESULTS

We developed a new random walk-based algorithm named prioritization with a warped network (PWN), which employs a warped network to achieve enhanced performance. Network warping is based on both internal and external features: graph curvature and prior knowledge.

CONCLUSIONS

We showed that these compositive features synergistically increased the resulting performance when applied to random walk algorithms, which led to PWN consistently achieving the best performance among several other known methods. Furthermore, we performed subsequent experiments to analyze the characteristics of PWN.

摘要

背景

从无偏的高通量数据中提取有意义的信息是各个领域的一个挑战。具体来说,在药物发现的早期阶段,为了了解疾病生物学,需要生成大量数据以确定疾病靶点。已经应用了几种基于随机游走的方法来解决这个问题,但它们仍然存在局限性。因此,我们建议使用一种新的方法,通过随机游走来增强高通量数据分析的效果。

结果

我们开发了一种新的基于随机游走的算法,名为带有扭曲网络的优先级算法(PWN),它使用扭曲网络来实现增强的性能。网络扭曲基于内部和外部特征:图曲率和先验知识。

结论

我们表明,当应用于随机游走算法时,这些组合特征协同增加了最终的性能,这使得 PWN 在几种其他已知方法中始终能够实现最佳性能。此外,我们进行了后续实验来分析 PWN 的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/f901278b2abc/12859_2023_5227_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/b3b7978876ba/12859_2023_5227_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/ce472dcc3582/12859_2023_5227_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/870f37e7c9a1/12859_2023_5227_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/d6d07342ae36/12859_2023_5227_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/47d53f453842/12859_2023_5227_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/fe0fdf33de29/12859_2023_5227_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/765fda2f1f28/12859_2023_5227_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/3bc714908d72/12859_2023_5227_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/e1e0b877f07e/12859_2023_5227_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/d98ee4ef87bb/12859_2023_5227_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/f901278b2abc/12859_2023_5227_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/b3b7978876ba/12859_2023_5227_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/ce472dcc3582/12859_2023_5227_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/870f37e7c9a1/12859_2023_5227_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/d6d07342ae36/12859_2023_5227_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/47d53f453842/12859_2023_5227_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/fe0fdf33de29/12859_2023_5227_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/765fda2f1f28/12859_2023_5227_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/3bc714908d72/12859_2023_5227_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/e1e0b877f07e/12859_2023_5227_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/d98ee4ef87bb/12859_2023_5227_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cf/10031933/f901278b2abc/12859_2023_5227_Fig11_HTML.jpg

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2
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Sci Rep. 2022 Jun 27;12(1):10883. doi: 10.1038/s41598-022-14631-x.
3
Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility.
Comput Struct Biotechnol J. 2024 Jun 15;24:464-475. doi: 10.1016/j.csbj.2024.06.012. eCollection 2024 Dec.
利用全外显子测序和蛋白质相互作用网络对胚系皮肤黑色素瘤易感性的候选基因进行优先级排序。
Sci Rep. 2020 Oct 14;10(1):17198. doi: 10.1038/s41598-020-74293-5.
4
Identification of COVID-19 Infection-Related Human Genes Based on a Random Walk Model in a Virus-Human Protein Interaction Network.基于病毒-人类蛋白质相互作用网络中的随机游走模型鉴定与 COVID-19 感染相关的人类基因。
Biomed Res Int. 2020 Jul 8;2020:4256301. doi: 10.1155/2020/4256301. eCollection 2020.
5
uKIN Combines New and Prior Information with Guided Network Propagation to Accurately Identify Disease Genes.uKIN通过引导网络传播将新信息和先前信息相结合,以准确识别疾病基因。
Cell Syst. 2020 Jun 24;10(6):470-479.e3. doi: 10.1016/j.cels.2020.05.008.
6
Systematic comparison of the protein-protein interaction databases from a user's perspective.从用户角度对蛋白质-蛋白质相互作用数据库进行系统比较。
J Biomed Inform. 2020 Mar;103:103380. doi: 10.1016/j.jbi.2020.103380. Epub 2020 Jan 28.
7
Gene relevance based on multiple evidences in complex networks.基于复杂网络中多种证据的基因相关性。
Bioinformatics. 2020 Feb 1;36(3):865-871. doi: 10.1093/bioinformatics/btz652.
8
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9
A systematic approach to orient the human protein-protein interaction network.一种系统的方法来定向人类蛋白质-蛋白质相互作用网络。
Nat Commun. 2019 Jul 9;10(1):3015. doi: 10.1038/s41467-019-10887-6.
10
STRING v11: protein-protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets.STRING v11:具有增强覆盖范围的蛋白质-蛋白质相互作用网络,支持在全基因组实验数据集的功能发现。
Nucleic Acids Res. 2019 Jan 8;47(D1):D607-D613. doi: 10.1093/nar/gky1131.