BDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data

Abstract Background Birth defects pose a major challenge to infant health. Thus far, however, the causes of most birth defects remain cryptic. Over the past few decades, considerable effort has been expended on disclosing the underlying mechanisms related to birth defects, yielding myriad treatises...

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Autores principales: Dengwei Zhang, Si Zhou, Ziheng Zhou, Xiaosen Jiang, Dongsheng Chen, Hai-Xi Sun, Jie Huang, Shoufang Qu, Songchen Yang, Ying Gu, Xiuqing Zhang, Xin Jin, Ya Gao, Yue Shen, Fang Chen
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Lenguaje:EN
Publicado: BMC 2021
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Acceso en línea:https://doaj.org/article/b6a4d6d5fc68481f94d235876c9789e7
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spelling oai:doaj.org-article:b6a4d6d5fc68481f94d235876c9789e72021-11-07T12:06:46ZBDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data10.1186/s12920-021-01110-x1755-8794https://doaj.org/article/b6a4d6d5fc68481f94d235876c9789e72021-11-01T00:00:00Zhttps://doi.org/10.1186/s12920-021-01110-xhttps://doaj.org/toc/1755-8794Abstract Background Birth defects pose a major challenge to infant health. Thus far, however, the causes of most birth defects remain cryptic. Over the past few decades, considerable effort has been expended on disclosing the underlying mechanisms related to birth defects, yielding myriad treatises and data. To meet the increasing requirements for data resources, we developed a freely accessible birth defect multi-omics database (BDdb, http://t21omics.cngb.org ) consisting of multi-omics data and potential disease biomarkers. Results In total, omics datasets from 136 Gene Expression Omnibus (GEO) Series records, including 5245 samples, as well as 869 biomarkers of 22 birth defects in six different species, were integrated into the BDdb. The database provides a user-friendly interface for searching, browsing, and downloading data of interest. The BDdb also enables users to explore the correlations among different sequencing methods, such as chromatin immunoprecipitation sequencing (ChIP-Seq) and RNA sequencing (RNA-Seq) from different studies, to obtain the information on gene expression patterns from diverse aspects. Conclusion To the best of our knowledge, the BDdb is the first comprehensive database associated with birth defects, which should benefit the diagnosis and prevention of birth defects.Dengwei ZhangSi ZhouZiheng ZhouXiaosen JiangDongsheng ChenHai-Xi SunJie HuangShoufang QuSongchen YangYing GuXiuqing ZhangXin JinYa GaoYue ShenFang ChenBMCarticleBirth defectsChromosomal abnormalityOmicsBiomarkerInternal medicineRC31-1245GeneticsQH426-470ENBMC Medical Genomics, Vol 14, Iss 1, Pp 1-10 (2021)
institution DOAJ
collection DOAJ
language EN
topic Birth defects
Chromosomal abnormality
Omics
Biomarker
Internal medicine
RC31-1245
Genetics
QH426-470
spellingShingle Birth defects
Chromosomal abnormality
Omics
Biomarker
Internal medicine
RC31-1245
Genetics
QH426-470
Dengwei Zhang
Si Zhou
Ziheng Zhou
Xiaosen Jiang
Dongsheng Chen
Hai-Xi Sun
Jie Huang
Shoufang Qu
Songchen Yang
Ying Gu
Xiuqing Zhang
Xin Jin
Ya Gao
Yue Shen
Fang Chen
BDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data
description Abstract Background Birth defects pose a major challenge to infant health. Thus far, however, the causes of most birth defects remain cryptic. Over the past few decades, considerable effort has been expended on disclosing the underlying mechanisms related to birth defects, yielding myriad treatises and data. To meet the increasing requirements for data resources, we developed a freely accessible birth defect multi-omics database (BDdb, http://t21omics.cngb.org ) consisting of multi-omics data and potential disease biomarkers. Results In total, omics datasets from 136 Gene Expression Omnibus (GEO) Series records, including 5245 samples, as well as 869 biomarkers of 22 birth defects in six different species, were integrated into the BDdb. The database provides a user-friendly interface for searching, browsing, and downloading data of interest. The BDdb also enables users to explore the correlations among different sequencing methods, such as chromatin immunoprecipitation sequencing (ChIP-Seq) and RNA sequencing (RNA-Seq) from different studies, to obtain the information on gene expression patterns from diverse aspects. Conclusion To the best of our knowledge, the BDdb is the first comprehensive database associated with birth defects, which should benefit the diagnosis and prevention of birth defects.
format article
author Dengwei Zhang
Si Zhou
Ziheng Zhou
Xiaosen Jiang
Dongsheng Chen
Hai-Xi Sun
Jie Huang
Shoufang Qu
Songchen Yang
Ying Gu
Xiuqing Zhang
Xin Jin
Ya Gao
Yue Shen
Fang Chen
author_facet Dengwei Zhang
Si Zhou
Ziheng Zhou
Xiaosen Jiang
Dongsheng Chen
Hai-Xi Sun
Jie Huang
Shoufang Qu
Songchen Yang
Ying Gu
Xiuqing Zhang
Xin Jin
Ya Gao
Yue Shen
Fang Chen
author_sort Dengwei Zhang
title BDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data
title_short BDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data
title_full BDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data
title_fullStr BDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data
title_full_unstemmed BDdb: a comprehensive platform for exploration and utilization of birth defect multi-omics data
title_sort bddb: a comprehensive platform for exploration and utilization of birth defect multi-omics data
publisher BMC
publishDate 2021
url https://doaj.org/article/b6a4d6d5fc68481f94d235876c9789e7
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