Hello,

In my project i want to combine SNP array data with NGS data. We use the program Nexus 7.5. The goal is to see in one screen if the patiënt has on a certain genomic position an large indel(which you can detect with SNParray) and also a SNP (which you can detect with NGS). This is for the detection of for example compound heterozygous mutations.

My question is how can i do this in Nexus? I have already found something that you can load your sequence mutations as tracks. But is there a easier way? or maybe a complete other program? I am quite a newbie in this field.

Answers would mean a lot!! thanx,

Veenstra