b) Paired-ends reads - graphical overview - Paired-ends data allows for.'coverage graph' along the contig by clicking the checkbox in the Side To assist in this interpretation, CLC Genomics Workbench displays a.Reads data, coverage is one of the main resources for interpretation. a) Single reads - coverage and conflicts - When you only have single.454 and IlluminaĤ) Reference assembly of genomes of any size.ĥ) Assembly of standard read data and support for assembly of pairedĮnd reads / mate pair reads of any sequencing technology.Ħ) Advanced graphical tools for the detection of large scale mutations Reads, and it supports Sanger, 454, Solexa, Helicos, and SOLiDģ) Reference assembly of mixed datasets (e.g. Second, all the readsĪre assembled using the contig sequence as reference.Ģ) Reference assembly - The reference assembly of CLC Genomics Sequences are created by aligning all the reads. The de novo assembly process has two stages: First, contig Reads, and it supports Sanger, 454, Illumina Genome Analyzer, Helicos, Workbench supports both short and long reads, it supports paired-ends Workbench' (see G6G Abstract Number 20096A) and the followingġ) De novo assembly - The de novo assembly of CLC Genomics Integrating with the rest of your typical NGS workflow.ĬLC Genomics Workbench includes all features of 'CLC Main It incorporates cutting-edge technology and algorithms, while also supporting and Category Cross-Omics>Next Generation Sequence Analysis/ToolsĪbstract CLC Genomics Workbench is a new solution for analyzing and visualizing Next Generation Sequencing (NGS) data.