![]() For more information, send an e-mail to Ask a MolBio Librarian. Please register to receive instructions for accessing the software, as well as high performance computing options available with the HSLS MolBio Suite and the Center for Simulation and Modeling. Funding for CLC Genomics Workbench is provided by the University of Pittsburgh’s Institute for Personalized Medicine.ġ. Available for Windows, Mac OS X, and Linux platformsĢ. Supports all the major NGS platforms: SOLiD, Ion Torrent, Complete Genomics, 454, Illumina Genome Analyzer, and Sanger ![]() 4.Import the reference sequence and adapter list provided with the example data by going to: File Import Standard Import Ensure the option Automatic import is selected and select 'MT135044. CLC Genomics Workbench supports not only genomics analyses, but also transcriptomics, epigenomics, and classical sequence analyses. 3.Create a new folder for the project with a relevant name, for example, 'SARS-CoV-2 MinION Tutorial'. This resource is a comprehensive and user-friendly cross-platform desktop application for analyzing, comparing, and visualizing next generation sequencing (NGS) data. ![]() Attention University of Pittsburgh and UPMC researchers: The HSLS Molecular Biology Information Service is pleased to announce the availability of unlimited licenses for CLC Genomics Workbench from CLC bio.
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