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Notably, KpBest and cBest1 have very similar structures, although the former shares a much lower sequence identity (14%) with hBest1 compared to the latter (74%).
The primase C-terminal domain has much lower sequence homology compared to the rest of the primase domain or even its interacting counterpart helicase NTD (Figure S5).
The structure is similar to another protein of much lower sequence homology, the E coli chaperone Hsp31 [ 10, 20].
We find that across the genus Anopheles, lncRNAs display much lower sequence conservation than protein-coding genes.
Most previous studies of KS diversity in dinoflagellate transcriptomes had much lower sequence depth and coverage, therefore similar sequences may be present in other species, but have not been detected.
We find that the lncRNA gene set exhibits much lower sequence conservation across anophelines, when compared with either previously annotated protein-coding genes or protein-coding genes discovered in our study.
Similar(50)
Therefore, we also consider much lower sequencing error rate in our studies.
On the other hand, the Sultan data have a much lower sequencing depth and thus have a much lower threshold.
Also, we expect that a much lower sequencing coverage is required to compile representative k-mer lists than the coverage required for genome assembly.
If four samples are multiplexed, then approximately 50 million SRs per sample will be produced at a much lower sequencing cost per sample.
The species comparisons occupy a space between 24 and 73%, which is comparable to the one occupied by species comparisons for the DNA-A component (49%), except that it is much lower in sequence identity (about 16% lower).
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