Can investigators conducting GWAS as part of a clinical trial limit their data submission to baseline data only (i.e. data obtained prior to the start of the intervention)?
Related Questions
- Can investigators conducting GWAS as part of a clinical trial limit their data submission to baseline data only (i.e. data obtained prior to the start of the intervention)?
- Are there special laws or regulations about conducting research that clinical trial investigators need to be aware of?
- What is the IRBs role in submission of data to the NIH GWAS data repository?