Hello everyone

[linazel]

Hi, my name is Lina and I'm new to the SEQanswers site/forum and to the next-gen world as well
I'm a bit lost when it comes to next-gen seq and I'm hoping that you can help me make some sense in it all and later maybe I can be of service to others as well.
I study hereditary retinal degenerations and I'm doing my first exsome sequencing and was hoping that you could recommend me some tools for analysis.
Thanks,
Lina

PS I apologies for any spelling/grammar mistakes in advance, English is not my native tongue

[gprakhar]

What kind of analysis do you want to perform on the data?

[linazel]

I'm screening a patient to find a homozygous mutation, so I need to filter out all the SNPs and non pathogenic chages.