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• What method of fragmentation can I use in this workflow?
• What is the recommended insert size?
• What is the final library size?
• What is my expected final library yield?
• Are there any internal controls to test for methylation conversion?
• What is the min/max of DNA input for library preparation?
• Can I use the Standard Hybridization workflow for enrichment?
• Can I multiplex libraries in the capture; if so, what is the amount of library required?
• What modifications to the protocol can be made to optimize hybrid capture?
• What are the recommended number of amplification cycles post-capture?
• Should I use the Methylation Enhancer?