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Some mutations were genotyped by many combinations of probes, stringency and probe positions, while others were only genotyped by one probe length and assay condition.
Selected mutations were genotyped in 246 F2 animals using the Sequenom iPLEX assay service provided by Genomics Center at University of Minnesota.
Drug-resistant mutations were genotyped.
HIV-1 subtypes and pol gene drug resistance (DR) mutations were genotyped.
F2 segregating progeny from F1 plants that were heterozygous for all three mutations were genotyped for the SBEIIa mutations.
C282Y and H63D mutations were genotyped in a random sample of 3,798 individuals as described in details previously [ 15].
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Summary of results is shown in Table 2. Samples probed for the Factor II mutation were genotyped with 99.5% accuracy within a single assay, 100% accuracy if performed in triplicate.
n.t., not tested Briefly, DNA samples from 32 individuals in 7 families (three from North-Sardinia, two from Israel and two from Canada) carrying the BRCA2-8765delAG mutation were genotyped.
In the present case control study of BC, six SNPs in key genes involved in xenobiotic metabolism as well as in oestrogen synthesis and metabolism and BRCA1 founder mutation were genotyped to explore the possible relationship of these polymorphisms in the development of BC in Greenlandic Inuit women.
BAX T/C mutation in the intron 1 was genotyped as previously described [ 20], and BMPR1B C/G mutation was genotyped by PCR- SacII-RFLP method which was established in the present study.
Each mutation was genotyped separately.
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mutations were found
mutations were identified
mutations were selected
mutations were described
mutations were detected
mutations were verified
mutations were analyzed
mutations were eliminated
mutations were made
mutations were observed
mutations were confirmed
mutations were created
mutations were categorized
mutations were engineered
mutations were sequenced
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