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The range [Δmin, Δmax] is empirically calculated by analyzing the mapping span size distribution of the read pairs.
To evaluate the structure variation of FJ81278, possible inter-chromosomal translocation events were identified at the whole genome level by analyzing the mapping of paired-end reads.
Read count data are calculated by analyzing the mapping file where the reads have already been aligned to a reference genome.
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By analyzing the mapped reads from the MeDIP-seq in the Genome Analysis Toolkit (GATK) [ 68], we detected 3304 suggestive single nucleotide variations located within 900 bp windows centered over the p < 0.0001 DMRs (n = 852).
By analyzing the topographical map, the researchers could determine when objects struck existing craters, and they could measure the size of the objects.
By analyzing the PO maps, we are able to classify all possible singular points (the pinwheels) as having symmetries described by a small subset of the wallpaper groups.
These results were also confirmed by analyzing the TMS map data through an innovative approach based on the GLM.
The map positions were identified by analyzing the genotypes of the mapping populations for a genetic marker set of the M. truncatula genome [ 54, 55].
We next looked for a proof of the existence of birhythmicity by analyzing the first return map from and to the boundary between the domains D14 and D24 ([0, x) axis in Figure 10) which is crossed by both oscillatory regimes.
By analyzing the residue frequency map, more peaks are revealed than those obtained from the mouse anitsera, with the largest one with its FWHM spanning residues 22 125 with a small split around residue 60, and a medium one with its FWHM at residues 303 350 (Fig. 4, panel C, and Fig. S4).
Mate-pair sequencing was used to facilitate detection of larger insertion/deletion events (indels) by analyzing the distance between mapped reads of a pair (Korbel et al. 2007).
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