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Figure 2 | BMC Bioinformatics

Figure 2

From: CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

Figure 2

CNV Workshop query interface. Screenshot of the simple query interface in "annotated" mode for the CHOP CNV map database. Annotated mode enables a user to query by sample. Positional queries supported are chromosome(s), cytogenetic band(s), sequence position or range(s), and gene name(s). Most non-standard gene names are recognized and normalized to HGNC gene symbols. For the CHOP CNV map, additional searchable fields are CNV type (CNV, CNV region, or CNV block), ethnicity, and uniqueness (unique or non-unique/observed in multiple unrelated individuals).

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BMC Bioinformatics

ISSN: 1471-2105

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