Technology Core

技术核心

• 批准号: 8838714
• 负责人: Julie Dunning Hotopp
• 金额: $ 56万
• 依托单位: UNIVERSITY OF MARYLAND BALTIMORE
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8838714
• 关键词: Algorithms; Animal Model; Bacteria; Bioinformatics; Biological Assay; Cause of Death; Classification; Clinic; Code; Communicable Diseases; Communities; Cost Savings; Data; Data Analyses; Data Quality; Decision Trees; Detection; Development; Disease Outcome; Ensure; Evaluation; Gene Expression; Gene Expression Profile; Genetic Variation; Genome; Genomic Library; Genomics; High-Throughput Nucleotide Sequencing; Human; Imagery; Infectious Agent; Invertebrates; Libraries; Lung diseases; Measures; Metagenomics; Methodology; Methods; MicroRNAs; Microbe; Modification; Nucleic Acids; Online Systems; Open Reading Frames; Orthologous Gene; Parasites; Phylogeny; Population; Procedures; Production; Protocols documentation; Publications; Reading; Research; Research Personnel; Research Support; Resources; Ribosomal RNA; Sampling; Sequence Analysis; Shotguns; Specimen; System; Technology; Testing; Transcript; Transfer RNA; Vaccination; Vaccines; Variant; Viral; Virus; base; comparative genomics; cost; data integration; differential expression; fight against; fungus; gene function; genome analysis; genome sequencing; improved; metagenome; microbial genome; microbiome; novel; novel diagnostics; pathogen; tool; transcriptome sequencing; vector; virtual

Genomics has revolutionized research into infectious diseases and is poised to revolutionize the clinic. Through the activities in this technology core, we will provide high-throughput genome sequencing and analysis focused on understanding host, pathogen, and microbiome interactions as determinants of disease outcome. We will provide state-of-the-art, large-scale, high-throughput sequencing data for analysis of genomes, transcriptomes, metagenomes, metatranscriptomes, and microRNAs using the best methodologies and technologies available. We will use a portion of our combined annual sequencing capacity, which is now >38 terabases of high-quality, passed-filter data per year, to sequence infectious disease agents, their hosts, and their vectors. Continued cost savings while maintaining high quality and quantity sequencing will be obtained through: (a) the extensive use of standard operating procedures (SOPs) and (b) evaluation, development, and incorporation of enhancements, modifications and improvements as they become available. This will include the addition of new sequencing platforms, more efficient protocols, and more robust methodologies. In order to better sequence host/microbe mixed specimens, we propose to test targeted enrichment systems on PacBio genomic libraries and on lllumina transcriptome libraries to measure expression. We will continue to improve our abilities to assemble genomes/transcriptomes, identify open reading frames, and annotate gene function, particularly with respect to metagenome and metatranscriptome data. We will provide bioinformatic pipelines to analyze data types that transect multiple projects including measuring genetic variation in populations and communities. Comparative genomics will be enabled through pipelines for ortholog predictions and pan genome analyses. Transcriptome analyses will include RNAseq data alignment and visualization, differential expression analysis, heterogeneous RNAseq analysis, novel transcript identification, and miRNAseq analysis. Analysis of microbiome data will include analysis of 16S rRNA amplicons, whole metagenome shotgun classification, and metatranscriptome analysis. Stable, robust pipelines with the potential to have long lasting value will be implemented in the Cloud Virtual Resource (CloVR) to be distributed to the research community as easy-to-use virtual machines. When multiple data types are available, they will be integrated and visualized using Sybil and Circleator.

基因组学已经彻底改变了对传染病的研究，并准备彻底改变临床。