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Fig. 2 | BMC Bioinformatics

Fig. 2

From: GenESysV: a fast, intuitive and scalable genome exploration open source tool for variants generated from high-throughput sequencing projects

Fig. 2

The Interface of GenESysV and querying process. Querying process starts with the selection of study name, dataset name, and analysis type (a), followed by setting filters (b) and selecting variant/annotation related attributes (c). The output is a table displaying up to 400 records (d). The full results can be obtained by clicking the “Export to CSV” button (Top right)

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BMC Bioinformatics

ISSN: 1471-2105

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