CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics.
Xiaowu GaiJuan C. PerinKevin MurphyRyan O'HaraMonica D'arcyAdam WenocurHongbo M. XieEric F. RappaportTamim H. ShaikhPeter S. WhitePublished in: BMC Bioinform. (2010)
Keyphrases
- copy number
- high throughput
- single nucleotide polymorphisms
- microarray
- genome wide
- biological data
- systems biology
- high throughput technologies
- noise level
- data acquisition
- mass spectrometry data
- genomic data
- gene expression
- data mining
- protein protein interactions
- knowledge discovery
- clinical setting
- gene expression data
- monitoring system
- mass spectrometry
- image processing
- rna seq
- data sets