Full  Gene  Sequencing  refers    to    a      laboratory technique    used    to    determine     the    complete sequence    of   nucleotides   (the building blocks of DNA) in a  specific  gene   or   the  entire genome of an organism. This  process   allows   scientists   and healthcare providers to analyze the genetic code  in great   detail   to   identify  mutations,  variations,  or abnormalities that may be associated with diseases, inherited conditions, or other traits.