As it is clear in the title I am asking for advice
What is the first thing that I shall do when I receive the sequenced data for the genome am interested in,
like for example is there is a tool to check that the whole genome where sequenced probably? "there was no missing parts that was not sequenced". is the sequence good and I can proceed to the other steps? or I need to repeat something "like if some regions are not covered for example", and what is the other thing that I need to but in my consideration from your expertise and point of view.
Thanks in advance,