Download CLC Genomics Workbench 6.5 Build 94986 software

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An efficient and comprehensive software solution designed specifically for analyzing and sequencing samples of DNA as well as RNA data

Whats new in version 6.5 Build 94986:
New features:
Variant detection:
• New tool for adjusting read mappings through local realignment. The Local Realignment tool has the option to realign unaligned ends, realignment with a guidance variant track (e.g. obtained from external resources such as dbSNP, through the Indels and Structural Variants tool described below or from analysis of other read mappings) and allows for realignment of multiple samples. Has previously been available as a beta plugin.
• New tool for detecting structural variants (detects insertions and deletions, intra-chomosomal translocations, tandem duplications and inversions) working on "unaligned ends (soft clippings)". Has previously been available as a beta plugin.

• Important changes to variant reporting: adjacent variants are now reported as one variant instead of linked variants.
• A new variant filter has been added to both “Probabilistic Variant Detection” and “Quality-based Variant Detection”: “Ignore variants in non-speci...