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Metatranscriptomic Sequencing Service

With decades of experience in the fields of genomics sequencing, CD<br>Genomics is devoted to providing unprecedented amounts of microbial<br>metatranscriptomic data. Our strong expertise in the informative and unbiased<br>metatranscriptomic sequencing service is guaranteed by state-of-the-art high<br>throughput sequencers, flexible sequencing strategies, and professional<br>bioinformatics pipelines.

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Metatranscriptomic Sequencing Service

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  1. CONTACT 45-1 Ramsey Road, Shirley, NY 11967, USA Tel: 1-631-619-7922 Email: contact@cd-genomics.com Web: https://www.cd-genomics.com Metatranscriptomic Sequencing Service By CD Genomics With decades of experience in the fields of genomics sequencing, CD Genomics is devoted to providing unprecedented amounts of microbial metatranscriptomic data. Our strong expertise in the informative and unbiased metatranscriptomic sequencing service is guaranteed by state-of-the-art high throughput sequencers, flexible sequencing strategies, and professional bioinformatics pipelines. The Introduction of Metatranscriptomic Sequencing Metatranscriptomics is the culture-independent profiling (including protein- coding and non-coding DNA) of microbial community-wide gene expression, which is capable of monitoring RNA-based regulation and expressed biological signatures of complex bacterial communities in a given sample at a given moment and under specific conditions. It elucidates three aspects of a microbial community, including gene activity diversity, gene expression abundance, and differential gene expression analysis. The gene expression analysis can tell which genes exhibit the highest change in expression levels in different conditions potentially to identify biomarkers and expression signatures. While metagenomics shows us the microbial species present in the community and their genomic potentials, metatranscriptomics presents the function and activity of the complete set of transcripts, as well as community structure. Metatranscriptomics offers a more informative perspective compared with metagenomics in revealing active biochemical functions, which has become a focus for applications in the environmental, medical, and energy fields as well as the field of drug discovery. Advantages of Metatranscriptomic Sequencing A culture-free method to reveal the true extent of microbial diversity Permitting function-based activity screens More targeted than shotgun random sequencing Cost-efficient and time-effective • • • •

  2. CONTACT 45-1 Ramsey Road, Shirley, NY 11967, USA Tel: 1-631-619-7922 Email: contact@cd-genomics.com Web: https://www.cd-genomics.com • A wide range of applications, including basic research, ecological applications, clinical applications, industrial applications, and so on Metatranscriptomic Sequencing Workflow Our highly experienced expert team executes quality management following every procedure to ensure confident and unbiased results. The general workflow for metatranscriptomic sequencing is outlined below. After RNA isolation from qualified samples, rRNA depletion, library construction, high- throughput sequencing, and bioinformatics analysis are in turn performed. We can help you make decisions on the library construction method, the depth of coverage, and the data analysis strategies based on your research aims. Service Specification

  3. CONTACT 45-1 Ramsey Road, Shirley, NY 11967, USA Tel: 1-631-619-7922 Email: contact@cd-genomics.com Web: https://www.cd-genomics.com CD Genomics provides full metatranscriptomic sequencing service package including sample standardization, library construction, Hiseq sequencing, raw data alignment, down-stream bioinformatics processing and statistical analysis. We can tailor this pipeline to your research interest. If you have additional requirements or questions, please feel free to contact us, our specialists are more than happy to assist you. Reference: 1. Warnecke F, Hess M. A perspective: metatranscriptomics as a tool for the discovery of novel biocatalysts. Journal of Biotechnology, 2009, 142(1): 91-95.

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