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Exact(7)
Table 1 reports the % of reads mapped from each dataset after the application of this selection criterion.
The table indicates the pathway category along with the pathway name and the number of genes mapped from each pathway.
Of all the reads, over 6.5 to 14 million reads could be mapped from each sample to mRNA specifically (Additional file 4).
Blood vessels were identified and a 10-pixel expansion was mapped from each blood vessel to create a mask to quantify leakage.
The number and properties of tRNAs mapped from each species to D. melanogaster are shown in table 1, and examples of ortholog sets with and without corresponding tRNA genes in D. melanogaster are shown in figure 1. Full mapping data in the form of GFF files are supplied in supplementary materials (Supplementary Material online).
Blood vessels were identified in panels a-c, a 10-pixel expansion was mapped from each blood vessel to create a mask and intensity was measured as shown in panel d, and blood vessel intensity was then subtracted as in panel e to generate blood brain barrier permeability quantification.
Similar(53)
We calculated the total number of mapped reads and the numbers of mapped reads from each chromosome library for each contig.
We first mapped reads from each species to the B. tryoni repeats, retaining reads with mapping quality q > 20.
Uniquely mapped reads from each replicate were assembled independently using the reference annotation based transcript (RABT) assembly method using Cufflinks.
We mapped reads from each isolate onto the reference genome using SSAHA v2.2.1 [ 17] with a minimum mapping score of 30.
2 In italics are the relative number of uniquely mapping piRNAs from each Ae. aegypti library.
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