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Genotoxicity test was conducted on the lung tissues using randomly amplified polymorphic DNA fingerprinting polymerase chain reaction (RAPD PCR) technique.
These techniques include sequence analysis of multicopy genes, restriction fragment length polymorphism, inter genic spacer regions, DNA fingerprinting, polymerase chain reaction (PCR), and randomly amplified polymorphic DNA [ 12– 15].
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As a molecular fingerprinting technique, polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) has been successfully applied to profile diverse microbial communities of various clinical specimens (Ariefdjohan et al. 2010; Oates et al. 2012; Walter et al. 2001; Weerasekera et al. 2017, 2013).
DNA fingerprinting methods such as polymerase chain reaction-denaturation gradient gel electrophoresis (PCR-DGGE) facilitate the microbial profiling of complex ecosystems including infected chronic wounds.
E. coli isolates from the blood and stool of patients with malignant diseases of the blood system were tested by DNA fingerprinting combined with a polymerase chain reaction (PCR) analysis of E. coli virulence factors.
We used genome fingerprinting simple sequence repeat-anchored polymerase chain reaction (PCR) amplification and random amplified polymorphic DNA PCR (RAPD PCR).
The clonotypes were determined by polymerase chain reaction-based fingerprinting.
Potential regulated genes were found using RNA arbitrarily primed polymerase chain reaction (RAP-PCR) and fingerprinting.
Spacer oligonucleotide (spoligotyping) analysis is a rapid polymerase chain reaction based method of DNA fingerprinting the Mycobacterium tuberculosis complex.
DNA fingerprinting methods for bacterial identification centre primarily on the use of the polymerase chain reaction (PCR).
Most information is obtained by cloning and sequencing the polymerase chain reaction (PCR) amplicons, but a more rapid analysis is achieved using fingerprinting techniques.
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