Due to the restricted degree of variation, we sequenced these loci from a subset of all individuals, again chosen to maximize geographic distribution across species.
To evaluate the distribution of the genetic variation, we sequenced two intergenic spacers of the chloroplastidial genome and one region of the nuclear ribosomal internal transcribed spacer (ITS).
To improve understanding of the factors influencing tuberculosis transmission and the role of pathogen variation, we sequenced all available specimens from patients diagnosed over 15 years in a whole district in Malawi.
To understand whether, or not, any life-history factors are linked to such variation, we sequenced the mt genomes of two species of blood-sucking lice that parasitize rats, Polyplax asiatica (Ferris 1923) and Polyplax spinulosa (Burmeister 1839).
In our investigation of the influence of double-strand break (DSB -mediated changes on genomic variation, we sequenceDSB -mediateded the mitochangesal genones of ecotypes Col-0 and Landsbergenomica (L er) and compared these with the publicly avariationC24 sequence (confirmed by resequencing).
In order to asses potential microsatellite variation, we sequenced both the GT25 repeat in DupA and the RS3 complex (CT 4TT CT 8 GT 24 repeat in DupB where applicable in rhesus macaques (n = 5), bonnet macaques (n = 4), orangutans (n = 5), gorillas (n = 9), and wild born chimpanzees (n = 25).
To understand whether, or not, any life-history factors are linked to such variation, we sequenced the mt genomes of Polyplax asiatica and Polyplax spinulosa, collected from the greater bandicoot rat, Bandicota indica, and the Asian house rat, Rattus tanezumi, respectively.
To investigate the association between wPip groups and mtDNA variation, we sequenced the cytb gene (that have been shown polymorphic in the Cx. pipiens complex, see [ 14]) in a subsample of 184 specimens from 101 Cx. pipiens natural populations and 44 isofemale laboratory lines.
To identify potentially functional genetic variations in PIK3R1, we sequenced the 5' and 3' regulatory domains, the exons and exon-intron boundaries of the gene.
To investigate the genetic variation underlying this morphological variation, we re-sequenced, assembled and annotated the genomes of two B. rapa subspecies, turnip crops (turnip) and a rapid cycling.
