Hi everybody!
I have a Multiple Sequence Alignment of several reads (amino acids) to a reference sequence (like mapping a sequence). Anyone knows how could I identify a point mutation??
That is, could I identify different isoforms??
Thanks a lot!!
jordi
I have a Multiple Sequence Alignment of several reads (amino acids) to a reference sequence (like mapping a sequence). Anyone knows how could I identify a point mutation??
That is, could I identify different isoforms??
Thanks a lot!!
jordi