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Intact protein analysis was carried out to quantify the glycosylation degree and profile the glycoform composition of all the prepared neo glycoconjugates, while pronase and chymotriptic digests were analyzed to map and rank the reactivity of protein residues.
Fifteen metaphases were analyzed to map each gene.
Two F2 populations of Ae. tauschii and three F2 populations from the synthetic wheat lines were analyzed to map the loci that control inhibition of wax production.
Genotype data and phenotype data from previous studies [ 14, 15, 21] were analyzed to map QTLs using the CIM method [ 40, 41], as implemented in version 2.5 of WinQTL Cartographer [ 42].
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Moreover, another important issue arises, whether a person was alive at the time of drowning (anti-mortem drowning) or he was thrown dead into the water body (post-mortem drowning) To answer these questions, phytoplankton species of forensic importance from two water bodies (Braham Sarovar and Prithus Pools) were analyzed to develop the Phytoplankton maps (P-maps).
Aligned reads were analyzed to determine if they mapped to unique or repetitive genomic regions, based on mapping qualities, or within protein-coding genes, based on genomic coordinates, using MATLAB (The MathWorks, Inc., Natick, MA).
Statistically significant (p ≤ 0.05) differentially expressed genes were analyzed to determine if they mapped to particular molecular functions, biological processes or pathways using Gene Ontology and Panther DB mapping tools.
DDE data were analyzed to derive spatially resolved maps of average axon diameter, ADD variance, and extra-axonal volume fraction, along with a novel sub-micron restricted structures map.
To examine how these 300 m2 variations influence landscape scale C estimates, historical and contemporary aerial photos were analyzed to develop forest density maps in order to estimate above ground PJ associated C stock changes in a 25 ha area.
High scoring food complements were analyzed to see if they mapped to a preferred USDA food group pairing.
SVs were analyzed to determine whether they mapped within genes, within exons, or partially overlapped exons.
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