Thank you GenoMax. If I understand correctly, it is possible to capture non-coding regions with hybridization technology, right? Are there any limitations with hybridization capture technology? (Other than repeated regions, which they say can be overcome with probe design) Last question (sorry I don't have wet lab experience at all): is hybrid capture sequencing capable of sequencing a full gene? The link you sent states "Regions of interest within the library are then captured using biotinylated oligonucleotide probes", but how extensive could the regions be?
Thank you!