Want to know in a nutshell; what information can be & can not be obtained by each of the whole genome molecular analysis approaches. Any book / paper / answer please? Thanks!
In very simple words, if you just want to see chromosomal aberrations then go for Array CGH, if you want to see point mutations in some selected group of genes then you may go for NGS gene panel sequencing, if you want to do exome for diagnostics then its OK. If you are still unable to identify your gene of choice then last option is whole genome sequencing.
The target gene sequencing ie. Sanger sequencing, arrayCGH and whole exome sequencing we have successfully used for our cases.