We need to determine whether PennCNV is appropriate and effective for analyzing data generated from low-resolution arrays (such as array-CGH with an overall median probe genomi spacing of 40-60 kb).
- Can PennCNV effectively handle data from this kind of low-resolution arrays?
- What are the limitations and challenges associated with using PennCNV for CNV detection in datasets with larger probe spacings?
- Are there any recommended adjustments or alternative approaches for analyzing CNVs in low-resolution array data?
- Are there any known studies or experiences demonstrating the effectiveness (or lack thereof) of PennCNV in this context?