crc's latest version of this workbench is exclusively made to work as standard ngs workbench for all users with no annoying errors. it also allows us to easily organize our data as well. you can directly save the output from any tool and any analysis as well as multiple sequences produced from multiple threads. it also allows us to share our data through the cloud. and it automatically updates every minute information about its recent changes with our 3 other workbenches. this program is the best software for all of the users who would like to analyze their ngs data easily. a new feature of clcgenomics workbench 7 is exome enrichment. it analyzes exome reads to provide a high quality set of exome sequences for downstream analysis, exome capture bias correction, and direct comparisons to exome sequence data from other animals and humans.
offers sequencing analysis, qc (quality controls), alignment, variation identification, annotation, etc. easy to use, powerful and complete. supports all major ngs platforms, including hiseq/miseq, solid and ion torrent. small memory footprint allows simultaneous analysis of hundreds of samples. supports fastq, bam, vcf, sam, fasta, xml, bed, bigwig. publishes reports directly to the web, csv, html, xml, table and other formats. you can also save your data in new fastq format with a higher quality of storage. metadata tags also allow you to quickly organize, access and visualize data. with clcgenomics workbench, you can perform qc checks and genome assembly from raw sequence data, as well as sequence matching against non-redundant and/or personal databases. it is very useful for data backup and data management. 3d9ccd7d82