Making sense of complex metagenomic data becomes easy through tools and streamlined analysis workflows for taxonomic and functional microbiome analysis.

Clc Genomics Workbench Free Genome Browser

With version 11, CLC Genomics Workbench can now be used as a free genome browser to share, view, and explore NGS analysis results.

Enjoy support for a wide range of open and proprietary file formats.

Its cutting-edge technology incorporates unique features and algorithms that are widely used by scientific leaders in industry and academia to overcome bottleneck challenges associated with data analysis.

All the tools you need, integrated into a single user friendly and scalable application, and ready to generate results you can trust.

Powered by cutting-edge technology and accelerated algorithms CLC Genomics Workbench supports a comprehensive set of NGS data analysis applications.

Resequencing CLC Genomics Workbench supports the complete resequencing pipeline for detecting and comparing genetic variants.

When dealing with high sample volumes efficient algorithms reduce run time while customizable analysis workflows and batch processing shorten hands-on time to a minimum.

CLC Genomics Workbench allows you to focus on the biological interpretation of detected variants.

Read mapping The first step in resequencing is accurate read mapping.

Our algorithm is optimized for high-quality mapping of large data volumes in a fast and memory-efficient way.

The algorithm offers comprehensive support for a variety of data formats, including both short and long reads, and all flavors of paired read data regardless of insert size or read orientation.

Local realignment can drastically reduce false positive detection rates for certain variant types.

Clc Genomics Workbench Manual Work And

Our goal is to reduce your manual work and focus on deriving biological meaningful results from raw NGS reads.

Workflow Workflows streamline selected tools into one analysis.

Workflows can be run in batch making them a powerful tool for processing large numbers of samples with minimal user interventions.

You can easily set up your own workflows and create and share workflow installer files with colleagues or other researchers following your scientific publications.

Commercial add-ons introduce preconfigured example workflows to get you from data to publication faster.

Like for our read mapper, a wide range of NGS data types is supported, and hybrid assemblies combine the unique strength of short and long reads for optimal results.

If assembly of long reads (like PacBio) or genome finishing are the primary focus, then CLC Genomics Workbench can be enhanced with the commercial CLC Genome Finishing Module.

RNA-Seq The free Advanced RNA-Seq plugin integrates all the analysis steps from secondary analysis of the reads to sophisticated statistics into easy-to-use workflows, and gives access to a wide range of experimental designs, from case-control or multi-group experiments to multi-factorial experiments.

All tools account for differences due to sequencing depth, removing the need to normalize input data.

Multi-factorial statistics control for batch effects and support paired studies.

Statistical results can be visualized in a genomic context as tracks, in a table view, or through the many visualization options leveraging metadata: volcano plots, 2D Heatmaps, Principal Component Analysis and Venn diagrams.

Metagenomics Uncover critical correlations between microbiota, its metagenome, and host.

Clc Genomics Workbench Crack