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Assessing wildfire risk entails the integration of fire modeling outputs, maps of highly valued resources and assets (HVRAs), characterization of fire effects, and articulation of relative importance across HVRAs.
In silico ground-truthing would be particularly useful for biome maps of highly environmentally heterogeneous areas such as the Andes.
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The first research question is whether the HSM can produce an accurate map of highly attractive places at a national level.
Comprehensive transcriptional and chromatin mapping of highly pure endodermal populations revealed that endodermal enhancers existed in a surprising diversity of "pre-enhancer" states before activation, reflecting the establishment of a permissive chromatin landscape as a prelude to differentiation.
Hence, it would be expected that circuits operating at the state ON were preferentially based on I3-FFL and I4-FFL and were present within the regulatory map of highly demanded biological functions, such as central metabolism or transcription-translation machinery.
In polyploid crops, however, accurate SNP detection becomes challenging due to the ambiguous mapping of highly similar homeologous loci, which increases the false-positive rate of detected SNPs.
Structural mapping of highly conserved positions again recovers the starting pattern, although a few β-sheet-associated glycines have been replaced by charges on the most exposed loops.
The mapping of highly correlated phenotypes such as the relative content of total, saturated and unsaturated fat and lipid to protein ratio to the same narrow chromosomal region on Chr 12 suggests pleiotropic gene effects.
Other issues include biases resulting from the mapping of highly repetitive regions (Treangen and Salzberg 2011) and biases inherent in the sequencing protocol, for example, GC bias (Dohm et al. 2008) and PCR amplification bias (Aird et al. 2011).
Fortunately, using the low resolution cryo-EM reconstruction as the initial phase model and combining it with X-ray diffraction data by taking advantage of averaging electron density maps of the highly symmetrical virus particle, we were able to determine the HEV VLP structure to 3.5 Å resolution.
Figure 6 shows expression maps of several highly differentially expressed mouse endogenous retroviruses as well as a representative murine L1 and SINE.
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