![]() ![]() De novo assembly of all reads was conducted using 64-word size and 50 bubble. Make sure to join this webinar to elevate your understanding of current bioinformatics trends and get an overview of the latest capabilities of QIAGEN CLC Genomics Workbench. Mate pair and paired-end reads were trimmed using CLC Genomics Workbench v7.51. Read mapping of Sanger, 454, Illumina Genome Analyzer and SOLiD sequencing data. Analyzing and visualizing Next Generation Sequencing data, incorporates cutting-edge technology and algorithms, while also supporting and integrating with the rest of your typical NGS workflow. The training will cover the basics of data visualization, quality control (QC), creation of user-constructed. Homologous recombination deficiency (HRD) scoring and methylation profiling The CLC Genomics Workbench is the client software for the CLC Genomics Server. Introduction to QIAGEN CLC Genomics Workbench. ![]() Import RNA-seq expression data in a matrix format. ![]()
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