Suggestions(5)
Exact(6)
All protein coding genes associated with a regulatory mutation were analysed.
For plasma samples, only the exon 19 deletions, L858R point mutation and T790M point mutation were analysed.
V600E BRAF mutation were analysed after amplification of exon 15, using primers 5′-TGATCAAACTTATAGATATTGCACGA (upstream) and 5′- TCATACAGAACAATTCCAAATGC (downstream).
For that purpose, 14 microsatellites and one SNP spanning 4.98 Mb around the mutation were analysed in 10 mutation carriers representing each family.
When cell lines known to be homozygous for specific mutation were analysed, PCR products were mixed 1 : 1 with PCR products of a wild-type cell line, denatured by heating, and slowly renatured to generate heteroduplexes.
Genomic DNA from 131 formalin-fixed paraffin-embedded (FFPE) tumors (luminal A and B, HER2+ and triple negative BC) with known BRCA1 mutation status or unscreened for BRCA1 mutation were analysed by array Comparative Genomic Hybridization (array CGH).
Similar(54)
The ADAMTS10 missense mutation was analysed in silico, with conflicting results as to its effects on protein function, but it was predicted to affect the leader sequence.
DNA sequencing of genomic and cDNA PCR products was performed in both directions and the position of the putative mutation was analysed individually for each PCR product.
The IVS2+1G>A and I157T variants in CHEK2 were detected using restriction fragment length polymorphism PCR analysis, and the 1100delC mutation was analysed using allele-specific oligonucleotide PCR.
The correlation between the variation of HV interval (HV2 HV1) and the size of the mutation was analysed using the linear regression method.
Each allele with either a nonsense or essential splice mutation is analysed for morphological differences during the first 5 days of development.
More suggestions(15)
mutant were analysed
mutation were treated
mutation were assigned
mutation were grouped
mutation were undertaken
mutation were identified
mutation were labelled
mutation were included
mutation were classified
mutation were detected
mutation were generated
mutation was analysed
mutation were amplified
mutation were proposed
mutation were performed
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com