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Exact(9)
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.
The -151C/T mutation was genotyped in the 15,854 Danes with a minor allele frequency of 0.01%.
pfcrt codon 76 point mutation was genotyped by nested PCR and restriction fragment-length polymorphism analysis.
The Grey mutation was genotyped with long range PCR as previously described [ 2].
The IGF2-intron3-G3072A mutation was genotyped for most of the F0 and F1 founders of both pedigrees (Table 1).
Similar(51)
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.
Selected mutations were genotyped in 246 F2 animals using the Sequenom iPLEX assay service provided by Genomics Center at University of Minnesota.
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.
Related(20)
mutation was described
mutation was detected
mutation was labeled
mutation was confirmed
mutation was repeated
mutation were genotyped
mutation was created
mutation was backcrossed
mutation was expected
mutation was introduced
mutation was termed
mutation was found
mutation was named
mutation was identified
mutation was used
mutation was mapped
mutation was transformed
mutation was generated
mutation was examined
mutation was verified
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