CLC Genomics Workbench 7.5.1
Allows you to analyze and visualize various genomic sequences
CLC Genomics Workbench's architecture makes use of cutting-edge technology and algorithms, and is also able to support and integrate with the classical NGS workflow.
CLC Genomics Workbench supports de novo assembly, SNP detection and sizable number of downstream analysis.
CLC Genomics Workbench's design enables you to conduct reference assembly of genomes regardless of their size.
- Read mapping
- De novo assembly
- Variant Detection
- Trio Analysis
CLC Genomics Workbench
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What's New in This Release:
- New features and improvements:
- "Filter Annotations on Name" can now insert names to filter on from significantly bigger files. Previously the limit for the file size was 10KB, this has now been increased to 20MB.
- RNA-Seq Analysis: The ENSEMBL gene id of each gene, where available, has been added as an additional column to the gene expression track output.
- Improved performances of the ChIP-seq Analysis tool for genomes with a large number of chromosomes.