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In this approach, we mapped the human phenotypes associated with GWAS-discovered loci to their corresponding mouse phenotypes, and we assembled a comprehensive list of mouse genes associated with these phenotypes.
In the second approach, we mapped the changes triggered by HDACi to the human TF network.
Using this approach, we mapped and cloned the DNA from 13 interband regions.
In this study using the ECP approach, we mapped potential hidden identity elements that discriminate the 20 different tRNA identities.
Using a molecular landmark-guided fluorescent in situ hybridization approach, we mapped 624 Mb of the Ae. aegypti genome to mitotic chromosomes.
In the transcriptome-based approach, we mapped transcriptome reads to the assembly using TopHat (version 1.3.1) [ 20], which can align reads across splice junctions.
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Interestingly, with the bi-parental mapping approach, we also mapped QTLGLSchr8 (Table 3) to the bins 8.02-8.04, wasconsistentsistent with Zhang et al. [ 40].
In this approach we first mapped raw reads to the TR to achieve faster mapping and SNP-calling, due to the smaller reference sequence, and to detect more SNPs, due to mapping more reads into low-complexity regions and obtaining higher coverages.
Using this approach, we have mapped the functional interaction between the MID1-α4-PP2A MID1-α4-PP2A MID1-α4-PP2Aion between amino acomplex and 1100 (FiGLI3).
In the 'align-then-assemble' approach, we firstly mapped the RNA-Seq reads from each tissue to the reassembled cucumber genome using Bowtie [ 21] and the spliced aligner TopHat [ 22].
Using double immunostaining approach, we first mapped the maturation profile of IO neurons that encoded gravity-related movements in 3-D and then the expression pattern of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) and N-methyl d-aspartate (NMDA) receptor subunits in these functionally identified neurons.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com