Entire genome sequencing is apparently the way toward deciding the total DNA arrangement of a life form's genome at a solitary time. This involves sequencing the entirety of a living being's chromosomal DNA just as DNA contained in the mitochondria and, for plants, in the chloroplast. By and by, genome successions that are almost finished are additionally called entire genome sequences.

Entire genome sequencing has to a great extent been utilized as an exploration apparatus, however was being acquainted with facilities in 2014. later on for customized medication, entire genome succession information might be a significant device to manage remedial intervention. The device of quality sequencing at SNP level is likewise used to pinpoint useful variations from affiliation examines and improve the information accessible to specialists keen on developmental science, and subsequently may establish the framework for anticipating infection defenselessness and medication reaction.

Entire genome sequencing ought not be mistaken for DNA profiling, which just decides the probability that hereditary material originated from a specific individual or gathering, and doesn't contain extra data on hereditary connections, beginning or powerlessness to explicit diseases. also, entire genome sequencing ought not be mistaken for strategies that grouping explicit subsets of the genome - such techniques incorporate entire exome sequencing (1-2% of the genome) or SNP genotyping (<0.1% of the genome). Starting at 2017 there were no finished genomes for any well evolved creatures, including people. Between 4% to 9% of the human genome, for the most part satellite DNA, had not been sequenced.