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The mapping data confirmed that Clementine arose from hybridization between 'Mediterranean' mandarin and sweet orange.
Mapping data confirmed the high diversity of the 24-nt sRNA sequences previously mentioned in total reads counting.
Genetic mapping data confirmed that the Clementine is a hybrid between the 'Mediterranean' mandarin and sweet orange.
Optical mapping data confirmed that paced beats propagated as elliptical wavefronts that emanated from the pacing electrode, even at high BPA concentrations.
The marker phase analysis performed from the Clementine and sweet orange mapping data confirmed this hypothesis, and allowed the identification of the haplotype structures of the mandarin and sweet orange gametes that produced the Clementine.
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Where available, deletion map data confirmed that these genes were located in centromeric chromosome bins (supplementary table S2, Supplementary Material online).
The comparison of the biomass maps with ground reference data confirmed the above findings but also demonstrated the difficulty to perform a consistent validation of remote sensing products.
Individually generated heat maps of the raw data confirmed such distinct patterns at raw measurement levels.
A heat-map representation of the SNP array data confirmed that the four amplified RTK (FGFR2, ERBB2, EGFR and MET) were mutually exclusive to one another (figure 3A).
It is noteworthy that although Esrp1 RNA levels are not completely absent in the Esrp1 KO RNA-seq samples by FPKM, mapped reads from the RNA-seq data confirmed that these RNAs represent transcripts splicing across the exon 7 9 deletion from exon 6 to exon 10, which would not encode a functional Esrp1 protein and reduced transcript levels are indicative of targeting by NMD.
Linkage data were merged with cytogenetic mapping data to confirm the order of markers or to identify linkage of isolated or weakly informative markers.
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