Workflows can be run in batch making them a powerful tool for processing large numbers of samples with minimal user interventions. Workflows streamline selected tools into one analysis. All made accessible through our tried and trusted interactive graphical user interface. Transcription factor ChIP-seq exposes defined peak regions characteristic of transcription binding sites throughout the whole genome. Recent improvements promise deeper insights into transcriptional regulation even in the absence of control sample. 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. 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.ĬLC Genomics Workbench supports the complete resequencing pipeline for detecting and comparing genetic variants. CLC Genomics Workbench is a powerful solution developed by scientists for scientists to analyze and visualize next generation sequencing (NGS) data.
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