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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.ĬLC Genomics Workbench offers a range of accurate variant detectors to detect single nucleotide variants (SNVs), multi-nucleotide variants (MNVs), small to medium sized insertions, deletions or replacements, as well as large structural variants. Multi-factorial statistics control for batch effects and support paired studies. All tools account for differences due to sequencing depth, removing the need to normalize input data. 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.

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Our goal is to reduce your manual work and focus on deriving biological meaningful results from raw NGS reads. Local realignment can drastically reduce false positive detection rates for certain variant types. It also supports the use of hybrid data sets. 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. Our algorithm is optimized for high-quality mapping of large data volumes in a fast and memory-efficient way. The first step in resequencing is accurate read mapping. 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.ĬLC Genomics Workbench allows you to focus on the biological interpretation of detected variants. RNA-seq and small RNA (miRNA, lncRNA) transcriptomics workflows for differential expression analysis at gene and transcript levels.ĬLC Genomics Workbench supports the complete resequencing pipeline for detecting and comparing genetic variants.

Supported NGS platforms are Illumina, IonTorrent, PacBio and GeneReader. Making sense of complex metagenomic data becomes easy through tools and streamlined analysis workflows for taxonomic and functional microbiome analysis. Uncover critical correlations between microbiota, its metagenome, and host.

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User-friendly bioinformatics software solutions allow for comprehensive analysis of your NGS data, including whole genome and transcriptome de novo assembly, targeted resequencing analysis, variant calling, ChIP-seq and DNA methylation (bisulfite sequencing analysis). Utilizing cutting-edge technology, unique features and algorithms widely used by scientific leaders in industry and academia to overcome challenges associated with data analysis.

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Download CLC Genomics Workbench 12.0.3 Full Version (crack keygen)CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow.