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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 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).
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).
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In an effort to identify these variations, we sequenced the transcriptomes of soybean seeds from nine lines varying in oil composition and/or total oil content.
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.
To further examine T. cruzi maxicircles and better understand their genetic variation, we amplified and sequenced the coding region of a clade A/DTU TcI representative Sylvio X10 to compare and contrast gene synteny and content.
Because one of the powerful advantages of new sequencing technologies is the ability to characterize sequence variation, we also determined the accuracy of RNA sequencing for discovering sequence variation.
To catalogue potentially relevant variation we first re-sequenced the entire mitochondrial genome of 159 patients.
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