Genome Trax
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Application data |
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| Biological application domain(s) | Structural variants |
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| Technology | Illumina |
| Created at | BIOBASE |
| Maintained? | Yes |
| Output format(s) | BED, GFF |
| Programming language(s) | Web-based |
| Licence | Commercial |
Summary: Genome Trax™ enables you to identify human genome variations of functional significance by mapping your NGS data to known elements such as disease mutations and regulatory sites.
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Description
- Prioritize mutations from whole exome or whole genome sequencing
- Uncover the impact of your human variants on disease risk, gene regulation, and protein function.
- Remove biologically irrelevant mutations and reduce the amount of mutations you have to investigate
- Identify novel mutations not previously reported in the literature
- Understand gene regulation changes in your variants by mapping novel mutations to known or predicted regulatory sites
- Find disease genes, drug targets, and pathways linked to your variations
Links
References
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