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. Homologous recombination deficiency (HRD) scoring and methylation profiling. Import RNA-seq expression data in a matrix format.Fast long-read assembly for Oxford Nanopore and PacBio reads from large eukaryotic genomes.Import data generated by MGI/BGI systems.Support for NGS data import from Amazon S3 and Illumina BaseSpace. CLC Genomics Workbench supports key next generation sequencing features within genomics, transcriptomics and epigenomics, and additionally it includes all the tools of CLC Main Workbench.
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