首页 > 最新文献

2016 International Conference on Bioinformatics and Systems Biology (BSB)最新文献

英文 中文
Count-based transcriptome analysis to identify differentially expressed genes for breast cancer 基于计数的转录组分析鉴定乳腺癌差异表达基因
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552147
R. Tripathi, Pawan Sharma, P. Chakraborty, P. Varadwaj
Sequencing the coding regions or the whole cancer transcriptome can provide valuable information about the differential expression patterns of the genes. Previous researches centered on ~2% of coding human genome, assuming that the non-coding sequences were “junk” lacking significant functional information. Recent medical research show that a major percentage of the human genome (~70-90%) are non-coding, stored in the cell in the form of non-coding RNA (ncRNA) which overshadows the coding information limited only to a small percentage. These ncRNAs are composed of mostly ultraconserved elements, lacking protein-coding potential and regulating gene expression acting as enhancers whose aberrant expression may be involved in pathological process such as cancer. Here, we have described RNA-seq data analysis for the profiling of transcriptome of Breast cells and provided a generic outline of the whole pipeline from next-generation sequencing (NGS) output for quantification of differential gene expression across different conditions (e.g., control vs test). We have used tool Cufflinks-Cuffdiff to estimate transcript-level expression for gene discovery extracted from high-throughput RNA-seq data across distinct conditions that represent candidate biomarkers for future research. This study provides the survey of coding transcripts associated genes expression within a cancer system.
对编码区或整个肿瘤转录组进行测序可以提供有关基因差异表达模式的有价值信息。以往的研究集中在约2%的编码人类基因组上,假设非编码序列是缺乏重要功能信息的“垃圾”。最近的医学研究表明,人类基因组的很大一部分(约70-90%)是非编码的,它们以非编码RNA (ncRNA)的形式储存在细胞中,掩盖了只有一小部分编码信息。这些ncrna大多由超保守元件组成,缺乏蛋白质编码潜能,作为增强子调节基因表达,其异常表达可能参与癌症等病理过程。在这里,我们描述了用于乳腺细胞转录组分析的RNA-seq数据分析,并提供了下一代测序(NGS)输出的整个管道的总体轮廓,用于量化不同条件下(例如,对照与测试)的差异基因表达。我们使用Cufflinks-Cuffdiff工具来估计从不同条件下的高通量RNA-seq数据中提取的基因发现的转录水平表达,这些数据代表了未来研究的候选生物标志物。本研究提供了癌症系统中编码转录本相关基因表达的调查。
{"title":"Count-based transcriptome analysis to identify differentially expressed genes for breast cancer","authors":"R. Tripathi, Pawan Sharma, P. Chakraborty, P. Varadwaj","doi":"10.1109/BSB.2016.7552147","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552147","url":null,"abstract":"Sequencing the coding regions or the whole cancer transcriptome can provide valuable information about the differential expression patterns of the genes. Previous researches centered on ~2% of coding human genome, assuming that the non-coding sequences were “junk” lacking significant functional information. Recent medical research show that a major percentage of the human genome (~70-90%) are non-coding, stored in the cell in the form of non-coding RNA (ncRNA) which overshadows the coding information limited only to a small percentage. These ncRNAs are composed of mostly ultraconserved elements, lacking protein-coding potential and regulating gene expression acting as enhancers whose aberrant expression may be involved in pathological process such as cancer. Here, we have described RNA-seq data analysis for the profiling of transcriptome of Breast cells and provided a generic outline of the whole pipeline from next-generation sequencing (NGS) output for quantification of differential gene expression across different conditions (e.g., control vs test). We have used tool Cufflinks-Cuffdiff to estimate transcript-level expression for gene discovery extracted from high-throughput RNA-seq data across distinct conditions that represent candidate biomarkers for future research. This study provides the survey of coding transcripts associated genes expression within a cancer system.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"454 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122938079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
In-silico structure prediction and domain characterization of inter alpha trypsin inhibitor heavy chain 4 胰蛋白酶抑制剂重链4的硅结构预测及结构域表征
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552125
Ankita Sharma, R. Malhotra, P. Kumari, S. Biswas, G. Soundhara Rajan
Altered expression of heavy chains of inter alpha trypsin inhibitor (ITI) family along with hyaluronan have clearly been established in various chronic inflammatory diseases. In the present study, the three dimensional (3D) model construction of ITIH4 and its functional role using Ginzu server was carried out. We identified three functional domains of ITIH4 protein model and elucidated their functional role. Thus, it helped us to understand the critical role of the protein in Serum derived Hyaluronic acid Associated Protein (SHAP) complex during the inflamed condition of RA.
在各种慢性炎症性疾病中,α -胰蛋白酶抑制剂(ITI)家族重链和透明质酸的表达明显改变。本研究利用Ginzu server进行了ITIH4的三维模型构建及其功能作用。我们鉴定了ITIH4蛋白模型的三个功能域,并阐明了它们的功能作用。因此,它有助于我们了解在RA炎症状态下血清衍生透明质酸相关蛋白(SHAP)复合物中该蛋白的关键作用。
{"title":"In-silico structure prediction and domain characterization of inter alpha trypsin inhibitor heavy chain 4","authors":"Ankita Sharma, R. Malhotra, P. Kumari, S. Biswas, G. Soundhara Rajan","doi":"10.1109/BSB.2016.7552125","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552125","url":null,"abstract":"Altered expression of heavy chains of inter alpha trypsin inhibitor (ITI) family along with hyaluronan have clearly been established in various chronic inflammatory diseases. In the present study, the three dimensional (3D) model construction of ITIH4 and its functional role using Ginzu server was carried out. We identified three functional domains of ITIH4 protein model and elucidated their functional role. Thus, it helped us to understand the critical role of the protein in Serum derived Hyaluronic acid Associated Protein (SHAP) complex during the inflamed condition of RA.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"95 12 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127989484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Meta-analysis of potential miRNA in Triticum astivum reveals their genome biased association with different metabolisms EST based potential miRNA identification in wheat 基于EST的小麦潜在miRNA鉴定表明,小麦潜在miRNA的基因组偏倚与不同代谢相关
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552126
D. Nigam, Puneet Kumar Kadimi, Sanjeev Kumar, D. Mishra, P. Pandey, Manoj Kumar singh, A. Rai, Subodh Kumar Sinha
MicroRNAs (miRNAs) are the key modulators implicated in the regulation of virtually every biological process found in multicellular eukaryotes. Wheat (Triticum aestivum) is one of the most important cereal crops worldwide. To date, only a few conserved miRNAs have been reported in wheat and their association with different metabolic process is still in dark. Therefore, the present study we attempt to predict miRNA and their association with metabolic pathways in wheat. Total 39 potential mature miRNA's were predicted using 1287279 ESTs of wheat and 8496 known mature miRNA's, along with their precursor sequences, of Viridiplantae. Overall, 11380 genome wise target genes across 21 chromosomes were identified and functionally characterized via meta-analysis. As a result, genome wise miRNA-targets signatures under different conditions and their regulatory pathways along with network structures were examined. Here, a concept of “miRNA community” was proposed and a miRNA community linked with nitrogen metabolism was identified. Top two potential miRNA's from this community were verified by stem loop pulsed RT-PCR for their expression in root and leaf tissue under nitrogen starvation. Exploration of such type of miRNAs communities will provide in depth understanding of metabolic processes that may leads to improved genotypes.
MicroRNAs (miRNAs)是多细胞真核生物中几乎所有生物过程的关键调节因子。小麦(Triticum aestivum)是全球最重要的谷类作物之一。迄今为止,在小麦中只报道了少数保守的mirna,它们与不同代谢过程的关联尚不清楚。因此,本研究我们试图预测miRNA及其与小麦代谢途径的关系。利用小麦的1287279个est和绿芽植物的8496个已知的成熟miRNA及其前体序列,共预测出39个潜在的成熟miRNA。总体而言,通过荟萃分析鉴定了21条染色体上的11380个基因组明智的靶基因,并对其进行了功能表征。因此,研究了不同条件下的基因组mirna靶标特征及其调控途径和网络结构。本文提出了“miRNA群落”的概念,并鉴定出与氮代谢相关的miRNA群落。通过茎环脉冲RT-PCR验证了该群落的前两个潜在miRNA在氮饥饿条件下在根和叶组织中的表达。对这类mirna群落的探索将提供对代谢过程的深入了解,从而可能导致基因型的改进。
{"title":"Meta-analysis of potential miRNA in Triticum astivum reveals their genome biased association with different metabolisms EST based potential miRNA identification in wheat","authors":"D. Nigam, Puneet Kumar Kadimi, Sanjeev Kumar, D. Mishra, P. Pandey, Manoj Kumar singh, A. Rai, Subodh Kumar Sinha","doi":"10.1109/BSB.2016.7552126","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552126","url":null,"abstract":"MicroRNAs (miRNAs) are the key modulators implicated in the regulation of virtually every biological process found in multicellular eukaryotes. Wheat (Triticum aestivum) is one of the most important cereal crops worldwide. To date, only a few conserved miRNAs have been reported in wheat and their association with different metabolic process is still in dark. Therefore, the present study we attempt to predict miRNA and their association with metabolic pathways in wheat. Total 39 potential mature miRNA's were predicted using 1287279 ESTs of wheat and 8496 known mature miRNA's, along with their precursor sequences, of Viridiplantae. Overall, 11380 genome wise target genes across 21 chromosomes were identified and functionally characterized via meta-analysis. As a result, genome wise miRNA-targets signatures under different conditions and their regulatory pathways along with network structures were examined. Here, a concept of “miRNA community” was proposed and a miRNA community linked with nitrogen metabolism was identified. Top two potential miRNA's from this community were verified by stem loop pulsed RT-PCR for their expression in root and leaf tissue under nitrogen starvation. Exploration of such type of miRNAs communities will provide in depth understanding of metabolic processes that may leads to improved genotypes.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"53 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114786886","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stilbene analogues as inhibitors of breast cancer Stem cells through P-glycoprotein efflux; A 3D quantitative structure-activity relationship study (Inhibitory activity of stilbenes analogues on breast cancer stem cells) 二苯乙烯类似物通过p -糖蛋白外排抑制乳腺癌干细胞二苯乙烯类似物对乳腺癌干细胞抑制活性的三维定量构效关系研究
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552134
A. Tripathi, K. Misra
Some stilbene analogues are essentially important for inhibiting the expression of P-glycoprotein in cancer stem cells. P-glycoprotein is a ATP binding cassette (ABC) transporter that mediates efflux process through ATP hydrolysis. This protein is composed of nucleotide binding and transmembrane domains. The expression level of P-glycoprotein is reported to be high in the cancer stem cell population. Stilbenes are phenylpropanoid-derived naturally occurring secondary metabolites of plants, reported as third generation inhibitors of P-glycoprotein. Based on biological activities of stilbenes against breast cancer cell line, the 3D quantitative structure-activity relationship and docking simulation study was carried out to predict the pharmacophoric features of these compounds. This study is likely to enable researchers to design and synthesize novel therapeutic analogues for reducing the growth of breast cancer stem cells by inhibiting the expression level of P-glycoprotein.
某些苯乙烯类似物对抑制肿瘤干细胞p -糖蛋白的表达具有重要作用。p -糖蛋白是ATP结合盒(ABC)转运体,通过ATP水解介导外排过程。该蛋白由核苷酸结合和跨膜结构域组成。据报道,p -糖蛋白在肿瘤干细胞群体中的表达水平较高。二苯乙烯是类苯丙烷衍生的植物次生代谢产物,被报道为第三代p糖蛋白抑制剂。根据二苯乙烯类化合物对乳腺癌细胞系的生物活性,进行三维定量构效关系和对接模拟研究,预测化合物的药效特性。这项研究可能使研究人员能够设计和合成新的治疗类似物,通过抑制p -糖蛋白的表达水平来减少乳腺癌干细胞的生长。
{"title":"Stilbene analogues as inhibitors of breast cancer Stem cells through P-glycoprotein efflux; A 3D quantitative structure-activity relationship study (Inhibitory activity of stilbenes analogues on breast cancer stem cells)","authors":"A. Tripathi, K. Misra","doi":"10.1109/BSB.2016.7552134","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552134","url":null,"abstract":"Some stilbene analogues are essentially important for inhibiting the expression of P-glycoprotein in cancer stem cells. P-glycoprotein is a ATP binding cassette (ABC) transporter that mediates efflux process through ATP hydrolysis. This protein is composed of nucleotide binding and transmembrane domains. The expression level of P-glycoprotein is reported to be high in the cancer stem cell population. Stilbenes are phenylpropanoid-derived naturally occurring secondary metabolites of plants, reported as third generation inhibitors of P-glycoprotein. Based on biological activities of stilbenes against breast cancer cell line, the 3D quantitative structure-activity relationship and docking simulation study was carried out to predict the pharmacophoric features of these compounds. This study is likely to enable researchers to design and synthesize novel therapeutic analogues for reducing the growth of breast cancer stem cells by inhibiting the expression level of P-glycoprotein.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"28 4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130779894","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Embryo and endosperm specific comparative transcriptome analysis of triticum aestivum in response to ABA and H2O2 stress ABA和H2O2胁迫下小麦胚和胚乳特异性比较转录组分析
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552157
Saurabh Gupta, Utkarsh Raj, Himansu Kumar, Pritish Kumar Varadwaj, Adhyana Gupta
Wheat seed germination directly affects wheat yield and quality. Embryo and endosperm are two main parts of wheat seed and plays crucial role in seed germination and subsequent plant growth and other development. In the process of seed germination a systematic bi-directional molecular interactions are major component and that got affected by the means of abiotic stresses. A variety of proteomic and transcriptomic approaches have been used so far to investigate seed germination process in response to abiotic stresses. In this study, we have investigated deferentially expressed genes/transcripts (DEGs) of embryo and endosperm in response to ABA and H2O2 stress by the means of stress systems biology approaches using microarray data. Further, role of DEGs in response to each stress was explored, which identify biological and molecular functions of genes during seed germination embryo and endosperm. Our results provide the insight into comparative transcriptomic mechanism of the embryo and endosperm in response to ABA and H2O2 treatment during seed germination process.
小麦种子发芽直接影响小麦的产量和品质。胚和胚乳是小麦种子的两个主要组成部分,在种子萌发和随后的植物生长发育中起着至关重要的作用。在种子萌发过程中,系统的双向分子相互作用是主要组成部分,并受到非生物胁迫的影响。迄今为止,各种蛋白质组学和转录组学方法已被用于研究种子萌发过程对非生物胁迫的响应。在这项研究中,我们利用微阵列数据,利用胁迫系统生物学的方法研究了胚胎和胚乳对ABA和H2O2胁迫的顺从表达基因/转录本(DEGs)。进一步探讨了基因在不同胁迫下的作用,确定了基因在种子萌发、胚和胚乳过程中的生物学和分子功能。我们的研究结果揭示了种子萌发过程中胚和胚乳对ABA和H2O2处理的转录组学比较机制。
{"title":"Embryo and endosperm specific comparative transcriptome analysis of triticum aestivum in response to ABA and H2O2 stress","authors":"Saurabh Gupta, Utkarsh Raj, Himansu Kumar, Pritish Kumar Varadwaj, Adhyana Gupta","doi":"10.1109/BSB.2016.7552157","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552157","url":null,"abstract":"Wheat seed germination directly affects wheat yield and quality. Embryo and endosperm are two main parts of wheat seed and plays crucial role in seed germination and subsequent plant growth and other development. In the process of seed germination a systematic bi-directional molecular interactions are major component and that got affected by the means of abiotic stresses. A variety of proteomic and transcriptomic approaches have been used so far to investigate seed germination process in response to abiotic stresses. In this study, we have investigated deferentially expressed genes/transcripts (DEGs) of embryo and endosperm in response to ABA and H2O2 stress by the means of stress systems biology approaches using microarray data. Further, role of DEGs in response to each stress was explored, which identify biological and molecular functions of genes during seed germination embryo and endosperm. Our results provide the insight into comparative transcriptomic mechanism of the embryo and endosperm in response to ABA and H2O2 treatment during seed germination process.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131139908","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
A bioinformatics study of miRNAs and their regulating targets in Curcuma longa (turmeric) 姜黄mirna及其调控靶点的生物信息学研究
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552160
Noopur Singh, S. Srivastava, Ashok Sharma
microRNAs are small, endogenous, noncoding RNA, work at post-transcriptional level and control the gene regulation in animals and plants. Turmeric is an Asian medicinal plant known for its medicinal properties. The present work focused on identification of the miRNAs take part in the developmental process of turmeric. Eight miRNA families (miR156, miR157, miR159, miR170, miR171, miR319, miR396 and miR5015) were identified by using bioinformatics approach. Phylogenetic analysis of selective miRNAs was performed. Six miRNA families were observed to regulate eighty-six target transcripts. Our results further indicated their role in binding, reproduction, stress and other developmental process. Gene annotation and pathway analysis illustrate the biological function of the targets regulated by the putative miRNAs. Involvement of miR156 and miR5015 in the regulation of rhizome development was also observed. Other miRNAs were found to be involved in the growth and developmental process of turmeric. To the best of our knowledge, this is the first report on miRNA prediction and regulation in turmeric.
microRNAs是一种小的、内源性的非编码RNA,在转录后水平起作用,控制动物和植物的基因调控。姜黄是一种亚洲药用植物,以其药用特性而闻名。本文主要对参与姜黄发育过程的mirna进行鉴定。采用生物信息学方法鉴定出8个miRNA家族(miR156、miR157、miR159、miR170、miR171、miR319、miR396和miR5015)。对选择性mirna进行系统发育分析。观察到6个miRNA家族调控86个靶转录物。我们的研究结果进一步说明了它们在结合、繁殖、应激等发育过程中的作用。基因注释和通路分析说明了被推测的mirna调控的靶标的生物学功能。还观察到miR156和miR5015参与根茎发育的调控。其他mirna也被发现参与了姜黄的生长发育过程。据我们所知,这是关于姜黄miRNA预测和调控的第一篇报道。
{"title":"A bioinformatics study of miRNAs and their regulating targets in Curcuma longa (turmeric)","authors":"Noopur Singh, S. Srivastava, Ashok Sharma","doi":"10.1109/BSB.2016.7552160","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552160","url":null,"abstract":"microRNAs are small, endogenous, noncoding RNA, work at post-transcriptional level and control the gene regulation in animals and plants. Turmeric is an Asian medicinal plant known for its medicinal properties. The present work focused on identification of the miRNAs take part in the developmental process of turmeric. Eight miRNA families (miR156, miR157, miR159, miR170, miR171, miR319, miR396 and miR5015) were identified by using bioinformatics approach. Phylogenetic analysis of selective miRNAs was performed. Six miRNA families were observed to regulate eighty-six target transcripts. Our results further indicated their role in binding, reproduction, stress and other developmental process. Gene annotation and pathway analysis illustrate the biological function of the targets regulated by the putative miRNAs. Involvement of miR156 and miR5015 in the regulation of rhizome development was also observed. Other miRNAs were found to be involved in the growth and developmental process of turmeric. To the best of our knowledge, this is the first report on miRNA prediction and regulation in turmeric.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"115 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133795873","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Modeling and simulation analysis of Salmonella typhimurium inside human epithelial cells: Host-pathogen relationship analysis by system biology 人上皮细胞内鼠伤寒沙门菌的建模和模拟分析:系统生物学的宿主-病原体关系分析
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552121
D. Arora, V. Singh, Ajeet Singh
Bacteria have the tendency to acquire resistance and develop defense from drug which makes pharmaceutical industries to work and develop new strategies for producing effective antibiotics against them. With molecular advancement and better understanding to their pathway architecture, channel for developing better antibiotics is open. Here we try to understand the enzyme kinetics of each protein and system biology of Salmonella typhi and infected host cell by its virulence factors. With taking in consideration, we have identified expressed protein CDC42, HiLD, and Arp2/3 complex protein in disease state when pathogen attacks the host. This study opens target for developing future drugs against salmonella typhi infection.
细菌对药物具有获得耐药性和发展防御的倾向,这使得制药工业努力并开发新的策略来生产有效的抗生素。随着分子的进步和对其途径结构的进一步了解,开发更好的抗生素的途径是开放的。本文试图通过其毒力因子了解伤寒沙门菌各蛋白的酶动力学和感染宿主细胞的系统生物学。考虑到这一点,我们鉴定出病原体攻击宿主时处于疾病状态的表达蛋白CDC42、HiLD和Arp2/3复合体蛋白。本研究为今后开发抗伤寒沙门氏菌药物开辟了靶点。
{"title":"Modeling and simulation analysis of Salmonella typhimurium inside human epithelial cells: Host-pathogen relationship analysis by system biology","authors":"D. Arora, V. Singh, Ajeet Singh","doi":"10.1109/BSB.2016.7552121","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552121","url":null,"abstract":"Bacteria have the tendency to acquire resistance and develop defense from drug which makes pharmaceutical industries to work and develop new strategies for producing effective antibiotics against them. With molecular advancement and better understanding to their pathway architecture, channel for developing better antibiotics is open. Here we try to understand the enzyme kinetics of each protein and system biology of Salmonella typhi and infected host cell by its virulence factors. With taking in consideration, we have identified expressed protein CDC42, HiLD, and Arp2/3 complex protein in disease state when pathogen attacks the host. This study opens target for developing future drugs against salmonella typhi infection.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"162 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131669717","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Copy number variation detection workflow using next generation sequencing data 使用下一代测序数据的拷贝数变异检测工作流程
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552117
Prashanthi Dharanipragada, N. Parekh
In the last decade, discovery of copy number variations (CNVs) have dramatically changed our understanding of differences between individuals. CNVs include both additional copies of sequence (duplications) and loss of genetic material (deletions) and provide an alternate paradigm for the genetic basis of human diseases. Genome-wide CNV detection is now possible using high-throughput, low-cost next generation sequencing (NGS) methods. Nature of NGS data demands various preprocessing and pretreatment steps before extracting any meaningful information. Among the plethora of variant calling methods available, R-based methods offer flexible environment, facilitating choice of various methods depending on the type of data or type of analysis to be performed. Here we give a pipeline for various steps involved in CNV detection in NGS data using R-based algorithms and packages.
在过去的十年中,拷贝数变异(CNVs)的发现极大地改变了我们对个体差异的理解。CNVs包括序列的额外拷贝(重复)和遗传物质的损失(缺失),并为人类疾病的遗传基础提供了另一种范式。使用高通量、低成本的下一代测序(NGS)方法,全基因组CNV检测现在成为可能。NGS数据的性质要求在提取有意义的信息之前进行各种预处理和预处理。在大量可用的变量调用方法中,基于r的方法提供了灵活的环境,便于根据数据类型或要执行的分析类型选择各种方法。在这里,我们给出了使用基于r的算法和包在NGS数据中进行CNV检测的各个步骤的管道。
{"title":"Copy number variation detection workflow using next generation sequencing data","authors":"Prashanthi Dharanipragada, N. Parekh","doi":"10.1109/BSB.2016.7552117","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552117","url":null,"abstract":"In the last decade, discovery of copy number variations (CNVs) have dramatically changed our understanding of differences between individuals. CNVs include both additional copies of sequence (duplications) and loss of genetic material (deletions) and provide an alternate paradigm for the genetic basis of human diseases. Genome-wide CNV detection is now possible using high-throughput, low-cost next generation sequencing (NGS) methods. Nature of NGS data demands various preprocessing and pretreatment steps before extracting any meaningful information. Among the plethora of variant calling methods available, R-based methods offer flexible environment, facilitating choice of various methods depending on the type of data or type of analysis to be performed. Here we give a pipeline for various steps involved in CNV detection in NGS data using R-based algorithms and packages.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"26 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125933219","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Glycolysis as a determinant of genome and proteome composition of different extremophilic archaea species 糖酵解是不同嗜极古菌基因组和蛋白质组组成的决定因素
Pub Date : 2016-03-04 DOI: 10.1109/BSB.2016.7552130
Ayon Pal, A. K. Bothra, Subhasis Mukhopadhyay
The archaea represents primitive earth dwellers confined mostly to very specialized and extreme habitats, and probably have evolved very early in the history of earth. Glycolysis is an excellent example of convergent evolution in archaea whereby a diversity of glucose degradation schemes exist. This study aims to unravel the strategies employed by different extremophilic species of archaea at the nucleotide and amino acid level to structure a genome as well as proteome, emphasizing particularly, on the glycolytic pathway of monosaccharide oxidation considering its antiquity and early appearance in evolution. We have tried to find out if linear sugar oxidation pathways like glycolysis in all its modified versions have somehow directed genome structuring in the extremophilic archaea. The study of comparative codon usage blueprint and codon pair preference might enable us to scrutinize the fact whether these organisms share any common codon or amino acid utilization outline or, this is entirely a function of their niche specific lifestyle.
古细菌代表了原始的地球居民,主要局限于非常特殊和极端的栖息地,可能在地球历史上很早就进化出来了。糖酵解是古细菌趋同进化的一个很好的例子,其中存在多种葡萄糖降解方案。本研究旨在揭示不同极端微生物物种在核苷酸和氨基酸水平上构建基因组和蛋白质组的策略,特别强调单糖氧化的糖酵解途径,考虑到它的古老和早期的进化。我们试图找出线性糖氧化途径,如糖酵解的所有修改版本,是否在某种程度上指导了嗜极古菌的基因组结构。比较密码子使用蓝图和密码子对偏好的研究可能使我们能够仔细检查这些生物是否共享任何共同的密码子或氨基酸使用大纲,或者这完全是它们特定生态位生活方式的功能。
{"title":"Glycolysis as a determinant of genome and proteome composition of different extremophilic archaea species","authors":"Ayon Pal, A. K. Bothra, Subhasis Mukhopadhyay","doi":"10.1109/BSB.2016.7552130","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552130","url":null,"abstract":"The archaea represents primitive earth dwellers confined mostly to very specialized and extreme habitats, and probably have evolved very early in the history of earth. Glycolysis is an excellent example of convergent evolution in archaea whereby a diversity of glucose degradation schemes exist. This study aims to unravel the strategies employed by different extremophilic species of archaea at the nucleotide and amino acid level to structure a genome as well as proteome, emphasizing particularly, on the glycolytic pathway of monosaccharide oxidation considering its antiquity and early appearance in evolution. We have tried to find out if linear sugar oxidation pathways like glycolysis in all its modified versions have somehow directed genome structuring in the extremophilic archaea. The study of comparative codon usage blueprint and codon pair preference might enable us to scrutinize the fact whether these organisms share any common codon or amino acid utilization outline or, this is entirely a function of their niche specific lifestyle.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"59 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126991996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A neural network based model of M and P LGN cells 基于神经网络的M和P LGN细胞模型
Pub Date : 2016-03-01 DOI: 10.1109/BSB.2016.7552165
Kuntal Ghosh
A new excitatory-inhibitory neural network model for the extended classical receptive field (ECRF) of Parvo (P), and Magno (M) cells in the lateral geniculate nucleus (LGN) is proposed. The model is based upon various well-known findings in neurophysiology, anatomy and psychophysics. The top-down linking of the proposed model to the feed-forward pathways, that is able to explain the simple, yet intriguing problem of brightness perception, may have implication in developing robust visual capturing and display systems, as well as in overall accurate representation of images as has been demonstrated in recent works.
提出了一种新的兴奋-抑制神经网络模型,用于研究外侧膝状核(LGN)中Parvo (P)和Magno (M)细胞的扩展经典感受野(ECRF)。该模型基于神经生理学、解剖学和心理物理学中各种众所周知的发现。所提出的模型与前馈路径的自上而下的联系,能够解释简单而有趣的亮度感知问题,可能对开发强大的视觉捕获和显示系统以及在最近的作品中所证明的图像的整体准确表示具有启示意义。
{"title":"A neural network based model of M and P LGN cells","authors":"Kuntal Ghosh","doi":"10.1109/BSB.2016.7552165","DOIUrl":"https://doi.org/10.1109/BSB.2016.7552165","url":null,"abstract":"A new excitatory-inhibitory neural network model for the extended classical receptive field (ECRF) of Parvo (P), and Magno (M) cells in the lateral geniculate nucleus (LGN) is proposed. The model is based upon various well-known findings in neurophysiology, anatomy and psychophysics. The top-down linking of the proposed model to the feed-forward pathways, that is able to explain the simple, yet intriguing problem of brightness perception, may have implication in developing robust visual capturing and display systems, as well as in overall accurate representation of images as has been demonstrated in recent works.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"14 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123646915","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
期刊
2016 International Conference on Bioinformatics and Systems Biology (BSB)
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1