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HMDD v2.0:一个实验支持的人类 microRNA 和疾病关联数据库。

HMDD v2.0: a database for experimentally supported human microRNA and disease associations.

机构信息

Department of Cell Biology, School of Basic Medical Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China, Department of Biomedical Informatics, School of Basic Medical Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China, Institute of Automation, Chinese Academy of Sciences, Beijing 100190, China and MOE Key Lab of Cardiovascular Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China.

出版信息

Nucleic Acids Res. 2014 Jan;42(Database issue):D1070-4. doi: 10.1093/nar/gkt1023. Epub 2013 Nov 4.


DOI:10.1093/nar/gkt1023
PMID:24194601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3964961/
Abstract

The Human microRNA Disease Database (HMDD; available via the Web site at http://cmbi.bjmu.edu.cn/hmdd and http://202.38.126.151/hmdd/tools/hmdd2.html) is a collection of experimentally supported human microRNA (miRNA) and disease associations. Here, we describe the HMDD v2.0 update that presented several novel options for users to facilitate exploration of the data in the database. In the updated database, miRNA-disease association data were annotated in more details. For example, miRNA-disease association data from genetics, epigenetics, circulating miRNAs and miRNA-target interactions were integrated into the database. In addition, HMDD v2.0 presented more data that were generated based on concepts derived from the miRNA-disease association data, including disease spectrum width of miRNAs and miRNA spectrum width of human diseases. Moreover, we provided users a link to download all the data in the HMDD v2.0 and a link to submit novel data into the database. Meanwhile, we also maintained the old version of HMDD. By keeping data sets up-to-date, HMDD should continue to serve as a valuable resource for investigating the roles of miRNAs in human disease.

摘要

人类 microRNA 疾病数据库(HMDD;可通过网站 http://cmbi.bjmu.edu.cn/hmdd 和 http://202.38.126.151/hmdd/tools/hmdd2.html 访问)是一个包含经过实验验证的人类 microRNA(miRNA)和疾病关联的集合。在这里,我们描述了 HMDD v2.0 的更新,为用户提供了几个新的选项,以方便在数据库中探索数据。在更新后的数据库中,miRNA-疾病关联数据被更详细地注释。例如,遗传学、表观遗传学、循环 miRNAs 和 miRNA 靶相互作用的 miRNA-疾病关联数据被整合到数据库中。此外,HMDD v2.0 还提供了更多基于 miRNA-疾病关联数据衍生的概念生成的数据,包括 miRNA 疾病谱宽度和人类疾病的 miRNA 谱宽度。此外,我们为用户提供了一个链接,可以下载 HMDD v2.0 中的所有数据,以及一个链接,可以将新数据提交到数据库中。同时,我们也保留了 HMDD 的旧版本。通过保持数据集的最新,HMDD 应该继续成为研究 miRNA 在人类疾病中的作用的有价值资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4d/3964961/ae4ed503b2f7/gkt1023f2p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4d/3964961/e16d25e32bcd/gkt1023f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4d/3964961/ae4ed503b2f7/gkt1023f2p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4d/3964961/e16d25e32bcd/gkt1023f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab4d/3964961/ae4ed503b2f7/gkt1023f2p.jpg

相似文献

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Brief Bioinform. 2025-7-2

[3]
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[4]
AMFCL: Predicting miRNA-Disease Associations Through Adaptive Multi-source Modality Fusion and Contrastive Learning.

Interdiscip Sci. 2025-6-2

[5]
RNA sequence analysis landscape: A comprehensive review of task types, databases, datasets, word embedding methods, and language models.

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[6]
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Comput Struct Biotechnol J. 2024-12-24

[7]
Establishing a GRU-GCN coordination-based prediction model for miRNA-disease associations.

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[8]
Predicting human miRNA disease association with minimize matrix nuclear norm.

Sci Rep. 2024-12-28

[9]
Prediction of miRNA-disease associations based on PCA and cascade forest.

BMC Bioinformatics. 2024-12-19

[10]
ACLNDA: an asymmetric graph contrastive learning framework for predicting noncoding RNA-disease associations in heterogeneous graphs.

Brief Bioinform. 2024-9-23

本文引用的文献

[1]
Similarity-based methods for potential human microRNA-disease association prediction.

BMC Med Genomics. 2013-4-9

[2]
SM2miR: a database of the experimentally validated small molecules' effects on microRNA expression.

Bioinformatics. 2012-12-5

[3]
SomamiR: a database for somatic mutations impacting microRNA function in cancer.

Nucleic Acids Res. 2012-11-24

[4]
ChIPBase: a database for decoding the transcriptional regulation of long non-coding RNA and microRNA genes from ChIP-Seq data.

Nucleic Acids Res. 2012-11-17

[5]
RWRMDA: predicting novel human microRNA-disease associations.

Mol Biosyst. 2012-10

[6]
Towards the understanding of microRNA and environmental factor interactions and their relationships to human diseases.

Sci Rep. 2012-3-16

[7]
Circulating microRNAs: novel biomarkers and extracellular communicators in cardiovascular disease?

Circ Res. 2012-2-3

[8]
TarBase 6.0: capturing the exponential growth of miRNA targets with experimental support.

Nucleic Acids Res. 2011-12-1

[9]
PolymiRTS Database 2.0: linking polymorphisms in microRNA target sites with human diseases and complex traits.

Nucleic Acids Res. 2011-11-10

[10]
Genome-wide identification of SNPs in microRNA genes and the SNP effects on microRNA target binding and biogenesis.

Hum Mutat. 2011-11-23

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