Download CLC Genomics Workbench Version 10.1.1 + crack

Download CLC Genomics Workbench Version 10.1.1 + crack

CLC Genomics Workbench is a powerful solution developed by scientists for scientists to analyze and visualize next generation sequencing (NGS) data. 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.

CLC Genomics Workbench is developed to support a wide range of NGS bioinformatics applications. The workbench is the ideal tool to generate custom workflows, and accelerate your data analysis. For instance, workflows can combine quality control steps, adapter trimming, read mapping, variant detection, and multiple filtering and annotation steps into a pipeline you can share with colleagues and execute with just one click.
Sequencing has become more affordable and data output is continuously increasing. Therefore, your bioinformatics platform needs to scale to your future sample throughput.

With CLC Genomics Server – the counterpart of CLC Genomics Workbench –  you can scale up as much as necessary and run data analysis on your server or high performance computer with ease. And for microbial research, Microbial Genomics Server Extension ensures that all tools you need for your microbial analyses can be simply plugged into CLC Genomics Server as well.

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.
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. It also supports the use of hybrid data sets. Local realignment can drastically reduce false positive detection rates for certain variant types. Our goal is to reduce your manual work and focus on deriving biological meaningful results from raw NGS reads.

Uncover critical correlations between microbiota, its metagenome, and host. Making sense of complex metagenomic data becomes easy through tools and streamlined analysis workflows for taxonomic and functional microbiome analysis. With commercial add-ons like CLC Microbial Genomics Module (hyperlink) the workbench turns into a leading solution for microbiologists.
And there is more:
With CLC Genomics Workbench you can enjoy more tools that belong into every bioinformatician’s repertoire. Enjoy a rich set of phylogenetic tools, create your own BLAST Searches, design PCR or real-time PCR primers, and take advantage of 10 years of molecular biology tool development.

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