CLC Genomics Workbench 7.5

Allows you to analyze and visualize various genomic sequences
CLC Genomics Workbench is an OS X application that helps you view and analyze Next Generation Sequencing data.

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.

Main features:

  • Resequencing
  • Workflow
  • Read mapping
  • De novo assembly
  • Variant Detection
  • RNA-Seq
  • ChIP-Seq
  • Trio Analysis

last updated on:
August 29th, 2014, 22:14 GMT
file size:
201.4 MB
developed by:
CLC bio
license type:
operating system(s):
Mac OS X 10.5 or later
binary format:
Intel only
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7 Screenshots
CLC Genomics Workbench - From CLC Genomics Workbench's main window you will be able to view, browse and analyze various genomic sequences.CLC Genomics Workbench - By accessing the Download menu, you can search and download specific genomic sequences from various databases.CLC Genomics Workbench - The Track tools menu enables you to create mapping graph tracks or GC content graph tracks.CLC Genomics WorkbenchCLC Genomics WorkbenchCLC Genomics WorkbenchCLC Genomics Workbench
What's New in This Release:
  • New features and improvements:
  • New tools:
  • New variant callers (Resequencing analysis):
  • Three new tools for detecting variants are available in the "Variant Detectors" toolbox under "Resequencing Analysis": Basic Variant Detection, Fixed Ploidy Variant Detection and Low Frequency Variant Detection. Basic Variant Detection and Fixed Ploidy Variant Detection are complete reimplementations of the Quality-based and Probabilistic Variant Detection tools, with improved options for filtering. The Low Frequency Variant Detection tool is a new statistically based tool for detecting low frequency variants e.g. in mixed tissue cancer or mixed population samples. The Quality-based and Probabilistic Variant Detection tools have been moved to the "Legacy tools" folder in the toolbox, and will eventually be retired.

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