A specialty database has been established at The Hong Kong University of Science and Technology to handle the chemical and biological data of medicinal plants and other natural products from scientific literatures. De...A specialty database has been established at The Hong Kong University of Science and Technology to handle the chemical and biological data of medicinal plants and other natural products from scientific literatures. Designed as a relational system capable of analyzing, comparing, and correlating data, the system can retrieve information in assimilated tabular formats. The database can provide information supports to researchers in the fields of medicinal chemistry, biochemistry, pharmacology, botany and other disciplines of natural products research.展开更多
In "Omics" era of the life sciences, data is presented in many forms, which represent the information at various levels of bio- logical systems, including data about genome, transcriptome, epigenome, proteome, metab...In "Omics" era of the life sciences, data is presented in many forms, which represent the information at various levels of bio- logical systems, including data about genome, transcriptome, epigenome, proteome, metabolome, molecular imaging, molec- ular pathways, different population of people and clinical/med- ical records. The biological data is big, and its scale has already been well beyond petabyte (PB) even exabyte (EB). Nobody doubts that the biological data will create huge amount of val- ues, if scientists can overcome many challenges, e.g., how to handle the complexity of information, how to integrate the data from very heterogeneous resources, what kind of principles or standards to be adopted when facing with the big data. Tools and techniques for analyzing big biological data enable us to translate massive amount of information into a better under- standing of the basic biomedical mechanisms, which can be fur- ther applied to translational or personalized medicine.展开更多
The investigation of the interplay between genes,proteins,metabolites and diseases plays a central role in molecular and cellular biology.Whole genome sequencing has made it possible to examine the behavior of all the...The investigation of the interplay between genes,proteins,metabolites and diseases plays a central role in molecular and cellular biology.Whole genome sequencing has made it possible to examine the behavior of all the genes in a genome by high-throughput experimental techniques and to pinpoint molecular interactions on a genome-wide scale,which form the backbone of systems biology.In particular,Bayesian network(BN)is a powerful tool for the ab-initial identification of causal and non-causal relationships between biological factors directly from experimental data.However,scalability is a crucial issue when we try to apply BNs to infer such interactions.In this paper,we not only introduce the Bayesian network formalism and its applications in systems biology,but also review recent technical developments for scaling up or speeding up the structural learning of BNs,which is important for the discovery of causal knowledge from large-scale biological datasets.Specifically,we highlight the basic idea,relative pros and cons of each technique and discuss possible ways to combine different algorithms towards making BN learning more accurate and much faster.展开更多
Since the official release of the stand-alone bioinformatics toolkit TBtools in 2020,its superior functionality in data analysis has been demonstrated by its widespread adoption by many thousands of users and referenc...Since the official release of the stand-alone bioinformatics toolkit TBtools in 2020,its superior functionality in data analysis has been demonstrated by its widespread adoption by many thousands of users and references in more than 5000 academic articles.Now,TBtools is a commonly used tool in biological laboratories.Over the past 3 years,thanks to invaluable feedback and suggestions from numerous users,we have optimized and expanded the functionality of the toolkit,leading to the development of an upgraded version—TBtools-II.In this upgrade,we have incorporated over 100 new features,such as those for comparative genomics analysis,phylogenetic analysis,and data visualization.Meanwhile,to better meet the increasing needs of personalized data analysis,we have launched the plugin mode,which enables users to develop their own plugins and manage their selection,installation,and removal according to individual needs.To date,the plugin store has amassed over 50 plugins,with more than half of them being independently developed and contributed by TBtools users.These plugins offer a range of data analysis options including co-expression network analysis,single-cell data analysis,and bulked segregant analysis sequencing data analysis.Overall,TBtools is now transforming from a stand-alone software to a comprehensive bioinformatics platform of a vibrant and cooperative community in which users are also developers and contributors.By promoting the theme“one for all,all for one”,we believe that TBtools-II will greatly benefit more biological researchers in this big-data era.展开更多
Hepatocellular carcinoma(HCC),one of the most common gastrointestinal cancers,has been considered a worldwide threat due to its high incidence and poor prognosis.In recent years,with the continuous emergence and promo...Hepatocellular carcinoma(HCC),one of the most common gastrointestinal cancers,has been considered a worldwide threat due to its high incidence and poor prognosis.In recent years,with the continuous emergence and promotion of new sequencing technologies in omics,genomics,transcriptomics,proteomics,and liquid biopsy are used to assess HCC heterogeneity from different perspectives and become a hotspot in the field of tumor precision medicine.In addition,with the continuous improvement of machine learning algorithms and deep learning algorithms,radiomics has made great progress in the field of ultrasound,CT and MRI for HCC.This article mainly reviews the research progress of biological big data and radiomics in HCC,and it provides new methods and ideas for the diagnosis,prognosis,and therapy of HCC.展开更多
It is widely recognized that exchange, distribution, and integration of biological data are the keys to improve bioinformatics and genome biology in post-genomic era. However, the problem of exchanging and integrating...It is widely recognized that exchange, distribution, and integration of biological data are the keys to improve bioinformatics and genome biology in post-genomic era. However, the problem of exchanging and integrating biological data is not solved satisfactorily. The extensible Markup Language (XML) is rapidly spreading as an emerging standard for structuring documents to exchange and integrate data on the World Wide Web (WWW). Web service is the next generation of WWW and is founded upon the open standards of W3C (World Wide Web Consortium) and IETF (Internet Engineering Task Force). This paper presents XML and Web Services technologies and their use for an appropriate solution to the problem of bioinformatics data exchange and integration .展开更多
Network or edge biomarkers area reliable form to characterize phenotypes or diseases.However,obtaining edges orcorrelations between molecules for an individual requires measurement ofmultiple samples of that individua...Network or edge biomarkers area reliable form to characterize phenotypes or diseases.However,obtaining edges orcorrelations between molecules for an individual requires measurement ofmultiple samples of that individual,which are generally unavailable in clinical practice.Thus,it is strongly demanded to diagnose a disease by edge or network biomarkers in one-sample-for-one-individual context.Here,we developed a new computational framework,EdgeBiomarker,to integrate edge and node biomarkers to diagnose phenotype of each single test sample.By applying the method to datasets of lung and breast cancer,it reveals new marker genes/gene-pairs and related sub-networks for distinguishing earlier and advanced cancer stages.Our method shows advantages over traditional methods:(i)edge biomarkers extracted from non-differentially expressed genes achieve better cross-validation accuracy of diagnosis than molecule or node biomarkers from differentially expressed genes,suggesting that certain pathogenic information is only present at the level of network and under-estimated by traditional methods;(ii)edge biomarkers categorize patients into low/high survival rate in a more reliablemanner;(iii)edge biomarkers are significantly enriched in relevant biological functions or pathways,implying that the association changes ina network,rather than expression changes in individual molecules,tendtobe causally related to cancer development.The new frameworkof edgebiomarkers paves theway for diagnosing diseases and analyzing the irmolecular mechanisms by edges or networks in one-sample-for-one-individual basis.This also provides a powerful tool for precision medicine or big-data medicine.展开更多
文摘A specialty database has been established at The Hong Kong University of Science and Technology to handle the chemical and biological data of medicinal plants and other natural products from scientific literatures. Designed as a relational system capable of analyzing, comparing, and correlating data, the system can retrieve information in assimilated tabular formats. The database can provide information supports to researchers in the fields of medicinal chemistry, biochemistry, pharmacology, botany and other disciplines of natural products research.
基金partially supported by the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDB13040700)the National Program on Key Basic Research Project (973 Program, Grant No. 2014CB910504)the National Natural Science Foundation of China (NSFC) (Grant Nos. 61134013, 91130032, 61103075 and 91029301)
文摘In "Omics" era of the life sciences, data is presented in many forms, which represent the information at various levels of bio- logical systems, including data about genome, transcriptome, epigenome, proteome, metabolome, molecular imaging, molec- ular pathways, different population of people and clinical/med- ical records. The biological data is big, and its scale has already been well beyond petabyte (PB) even exabyte (EB). Nobody doubts that the biological data will create huge amount of val- ues, if scientists can overcome many challenges, e.g., how to handle the complexity of information, how to integrate the data from very heterogeneous resources, what kind of principles or standards to be adopted when facing with the big data. Tools and techniques for analyzing big biological data enable us to translate massive amount of information into a better under- standing of the basic biomedical mechanisms, which can be fur- ther applied to translational or personalized medicine.
基金We thank the support from the China National Science Foundation(Grant No.30890033,30588001 and 30620120433)Chinese Ministry of Science and Technology(No.2006CB910700)to J.D.J.H.
文摘The investigation of the interplay between genes,proteins,metabolites and diseases plays a central role in molecular and cellular biology.Whole genome sequencing has made it possible to examine the behavior of all the genes in a genome by high-throughput experimental techniques and to pinpoint molecular interactions on a genome-wide scale,which form the backbone of systems biology.In particular,Bayesian network(BN)is a powerful tool for the ab-initial identification of causal and non-causal relationships between biological factors directly from experimental data.However,scalability is a crucial issue when we try to apply BNs to infer such interactions.In this paper,we not only introduce the Bayesian network formalism and its applications in systems biology,but also review recent technical developments for scaling up or speeding up the structural learning of BNs,which is important for the discovery of causal knowledge from large-scale biological datasets.Specifically,we highlight the basic idea,relative pros and cons of each technique and discuss possible ways to combine different algorithms towards making BN learning more accurate and much faster.
基金supported by the Key Area Research and Development Program of Guangdong Province(2022B0202070003,and 2021B0707010004)supported by the National Science Foundation of China(#32072547,and#32102320)+5 种基金the National Key Research and Development Program(2021YFF1000101,and 2019YFD1000500)the Special Support Program of Guangdong Province(2019TX05N193)the Scientific Research Foundation of the Hunan Provincial Education Department(20A261),)the open competition program of top ten critical priorities of Agricultural Science and Technology Innovation for the 14th Five-Year Plan of Guangdong Province(2022SDZG05)C.C.is supported by the Guangzhou Municipal Science and Technology Plan Project(2023A04J0113)J.F.is supported by the Hainan Provincial Natural Science Foundation of China(323QN279).
文摘Since the official release of the stand-alone bioinformatics toolkit TBtools in 2020,its superior functionality in data analysis has been demonstrated by its widespread adoption by many thousands of users and references in more than 5000 academic articles.Now,TBtools is a commonly used tool in biological laboratories.Over the past 3 years,thanks to invaluable feedback and suggestions from numerous users,we have optimized and expanded the functionality of the toolkit,leading to the development of an upgraded version—TBtools-II.In this upgrade,we have incorporated over 100 new features,such as those for comparative genomics analysis,phylogenetic analysis,and data visualization.Meanwhile,to better meet the increasing needs of personalized data analysis,we have launched the plugin mode,which enables users to develop their own plugins and manage their selection,installation,and removal according to individual needs.To date,the plugin store has amassed over 50 plugins,with more than half of them being independently developed and contributed by TBtools users.These plugins offer a range of data analysis options including co-expression network analysis,single-cell data analysis,and bulked segregant analysis sequencing data analysis.Overall,TBtools is now transforming from a stand-alone software to a comprehensive bioinformatics platform of a vibrant and cooperative community in which users are also developers and contributors.By promoting the theme“one for all,all for one”,we believe that TBtools-II will greatly benefit more biological researchers in this big-data era.
基金supported by grants from the Natural Science Foundation of Fujian Province(2021J011283)a demonstration study on the application of domestic high-end endoscopy system and minimally invasive instruments for precise resection of hepatobiliary and pancreatic tumors(2022YFC2407304).
文摘Hepatocellular carcinoma(HCC),one of the most common gastrointestinal cancers,has been considered a worldwide threat due to its high incidence and poor prognosis.In recent years,with the continuous emergence and promotion of new sequencing technologies in omics,genomics,transcriptomics,proteomics,and liquid biopsy are used to assess HCC heterogeneity from different perspectives and become a hotspot in the field of tumor precision medicine.In addition,with the continuous improvement of machine learning algorithms and deep learning algorithms,radiomics has made great progress in the field of ultrasound,CT and MRI for HCC.This article mainly reviews the research progress of biological big data and radiomics in HCC,and it provides new methods and ideas for the diagnosis,prognosis,and therapy of HCC.
文摘It is widely recognized that exchange, distribution, and integration of biological data are the keys to improve bioinformatics and genome biology in post-genomic era. However, the problem of exchanging and integrating biological data is not solved satisfactorily. The extensible Markup Language (XML) is rapidly spreading as an emerging standard for structuring documents to exchange and integrate data on the World Wide Web (WWW). Web service is the next generation of WWW and is founded upon the open standards of W3C (World Wide Web Consortium) and IETF (Internet Engineering Task Force). This paper presents XML and Web Services technologies and their use for an appropriate solution to the problem of bioinformatics data exchange and integration .
基金This work was supported by the Strategic Priority Research Program of the Chinese Academy of Sciences(CAS)(No.XDB13040700)the National Program on Key Basic Research Project(No.2014CB910504)+1 种基金the National Natural Science Foundation of China(No.91439103,61134013,31200987)the Knowledge Innovation Program of SIBS of CAS(No.2013KIP218).
文摘Network or edge biomarkers area reliable form to characterize phenotypes or diseases.However,obtaining edges orcorrelations between molecules for an individual requires measurement ofmultiple samples of that individual,which are generally unavailable in clinical practice.Thus,it is strongly demanded to diagnose a disease by edge or network biomarkers in one-sample-for-one-individual context.Here,we developed a new computational framework,EdgeBiomarker,to integrate edge and node biomarkers to diagnose phenotype of each single test sample.By applying the method to datasets of lung and breast cancer,it reveals new marker genes/gene-pairs and related sub-networks for distinguishing earlier and advanced cancer stages.Our method shows advantages over traditional methods:(i)edge biomarkers extracted from non-differentially expressed genes achieve better cross-validation accuracy of diagnosis than molecule or node biomarkers from differentially expressed genes,suggesting that certain pathogenic information is only present at the level of network and under-estimated by traditional methods;(ii)edge biomarkers categorize patients into low/high survival rate in a more reliablemanner;(iii)edge biomarkers are significantly enriched in relevant biological functions or pathways,implying that the association changes ina network,rather than expression changes in individual molecules,tendtobe causally related to cancer development.The new frameworkof edgebiomarkers paves theway for diagnosing diseases and analyzing the irmolecular mechanisms by edges or networks in one-sample-for-one-individual basis.This also provides a powerful tool for precision medicine or big-data medicine.