Use of multi-core computers
Many tools in CLC Workbenches and Servers can make use of multi-core CPUs. This does not necessarily mean that all available CPU cores are used throughout the analysis. It means that these tools benefit from running on computers with multiple CPU cores.
Tools available differ between CLC Workbenches. In the table, the availability of these tools in different CLC Workbench Toolbox menus is indicated with an X.
Use of multi-core computers | Genomics | Drug Discovery | Cancer Research | |
Basic Variant Detection | X | X | ||
BLAST (will not scale well on many cores) | X | |||
Create Alignment | X | X | X | |
Create Detailed Mapping Report | X | X | ||
Create Sequencing QC Report (will not scale well on more than four cores) | X | |||
De Novo Assembly | X | |||
Dock Ligands | X | |||
Download Reference Genome Data | X | |||
Extract and Count | X | X | ||
Fixed Ploidy Variant Detection | X | X | ||
Import Molecules from SMILES or 2D | X | |||
K-mer Based Tree Construction | X | |||
Large Gap Read Mapper (currently in beta) | X | |||
Local Realignment | X | X | ||
Low Frequency Variant Detection | X | X | ||
Map Reads to Contigs | X | |||
Map Reads to Reference | X | X | ||
Maximum Likelihood Phylogeny | X | |||
Model Testing | X | |||
Probabilistic Variant Detection (legacy) | X | X | ||
QC for Sequencing Reads (will not scale well on more than four cores) | X | |||
Quality-based Variant Detection (legacy) | X | X | ||
RNA-Seq Analysis | X | X | ||
Screen Ligands | X | |||
Trim Sequences | X | X |