kilobasepairs

the human genome contains approximately three billion kilobasepairs of dna distributed across 23 chromosome pairs.

researchers sequenced a genetic region spanning fifteen kilobasepairs to identify disease-causing mutations.

the average gene in this organism consists of eight kilobasepairs, which is smaller than previously thought.

genome-wide association studies revealed that most quantitative trait loci span between one and fifty kilobasepairs.

scientists identified a regulatory element containing two kilobasepairs that controls gene expression patterns.

the deletion mutation removed approximately twenty kilobasepairs of genetic material from the chromosome.

phylogenetic analysis showed that this gene family expanded by adding multiple kilobasepairs over evolutionary time.

the plasmid vector can accommodate inserts up to ten kilobasepairs for recombinant dna experiments.

comparative genomics revealed that the two species differ by over one hundred kilobasepairs in their mitochondrial dna.

researchers calculated that the replication fork processes roughly two kilobasepairs per minute during dna synthesis.

the telomerase enzyme adds repetitive sequences of approximately six kilobasepairs to chromosome ends with each cell division.

whole-genome sequencing data indicated that structural variants greater than fifty kilobasepairs contribute significantly to genetic diversity.