dbNSFP(v2.9) is an integrated database of functional annotations for the human genome which compiles data from multiple sources to provide highly distilled information at both the variant* and gene level. The dbNSFP gene level annotation table can be imported into an ArrayStar project and accessed within the gene table, as well as used for advanced filtering.
*Note that for analysis at the variant level, Lasergene Genomics Suite offers a unique variant annotation database, which includes data from dbNSFP as well as
1000 Genomes. To learn more about incorporating the variant annotation database into your research, see our Variant Analysis Workflow.
- Download the following zipped file: dbNSFP2.9_gene.zip
- Decompress the zipped file.
- Open your ArrayStar project, choose File>Import Annotations and select the dbNSFP2.9_gene file from the decompressed dbNSFP folder.
Note: To add GO annotations to your dbNSFP annotation data, select the Data>Download Annotations... menu command.
- Liu X, Jian X, and Boerwinkle E. 2011. dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions. Human Mutation. 32:894-899.
- Liu X, Jian X, and Boerwinkle E. 2013. dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations. Human Mutation. 34:E2393-E2402.
- dbNSFP Database at the Jpopgen website.