Journal
GENOME MEDICINE
Volume 6, Issue -, Pages -Publisher
BMC
DOI: 10.1186/s13073-014-0074-6
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Funding
- Belgian National Fund for Scientific Research-Flanders (FWO), IWT/TBM [110700]
- Fondation Leducq
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Interpretation of the multitude of variants obtained from next generation sequencing (NGS) is labor intensive and complex. Web-based interfaces such as Galaxy streamline the generation of variant lists but lack flexibility in the downstream annotation and filtering that are necessary to identify causative variants in medical genomics. To this end, we built VariantDB, a web-based interactive annotation and filtering platform that automatically annotates variants with allele frequencies, functional impact, pathogenicity predictions and pathway information.
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