Hello everybody! I am a new member in this forum and I have a very basic call for help.
I beginning to set up an academic Clinical Genomics laboratory in Brazil. Our objective is to use whole exome sequencing as a service to unravel complex undiagnosed and rare diseases.
Could anyone help with suggestions of what should be our minimal IT infrastructure and the best software to be able to filter out common genomic variation, evaluate the potential pathogenic impact of mutations and visualize the filtered data?
Spena
I beginning to set up an academic Clinical Genomics laboratory in Brazil. Our objective is to use whole exome sequencing as a service to unravel complex undiagnosed and rare diseases.
Could anyone help with suggestions of what should be our minimal IT infrastructure and the best software to be able to filter out common genomic variation, evaluate the potential pathogenic impact of mutations and visualize the filtered data?
Spena