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The sessions were analysed with two different mapping functions, the Vienna Mapping Functions (VMF1) and GMF GPT2), and with or without using the information provided in the station log-files.
The regeneration behaviour of two different cooling ceilings with PCM was monitored and analysed with two different methods an analysis of the measured PCM temperatures as well as an analysis of the measured heat fluxes into and out of the PCM modules.
Samples were analysed with two different mass range settings: 350 850 and 850 2000 Da.
A total of 31 Spanish patients, who were previously tested for mutations with the ABCR400 microarray, were further analysed with two different techniques: dHPLC and MLPA.
RNA samples of the spleen, kidney, and liver were isolated from transgenic and non-transgenic fish and the expression datasets were analysed with two different data-mining tools.
MON810 and MON863 maize were analysed with two different reference genes; one method detecting ADH (from the MON863 method) and the other detecting hmg (from the MON810 method).
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Additionally, we performed polyribosomal profile analyses with two different doses of 5-azacytidine.
The non-homogenous (nh) PhyML nucleotide analyses with two different starting trees resulted in two different topologies.
To challenge the assumption of missing-at-random in the MI, we conducted sensitivity analyses with two different scenarios.
We conducted maximum parsimony (MP), ML and Bayesian inference (BI) analyses with two different taxon sets and two subsets of the data.
We performed phylogenetic analyses with two different data sets: concatenated amino acid and concatenated nucleotide sequences (without third codon positions) from all protein-coding genes.
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