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This sample resulted from taking the freshman students from a larger sample (described below; N = 1,980) and first selecting the students who identified as currently engaging in nonsuicidal self-injury (NSSI).
In the second mailing sample (described below), we attempted to contrast HURT factor scores across headache types to assess relative performance.
To identify tracts of IBD, we implemented the approach of Pool et al. (2012), but with slight modifications for the diploid genomes and for the large DPGP3 population sample (described below).
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Prior to the analysis of the paint cross-sections, powdered reference samples (described below) were prepared for bulk XANES analysis by dusting the finely ground powder onto sulfur-free Kapton tape.
The maximum activity in the VC region was measured at all time points, and the resulting blood TAC was shifted in time (+10 s) to match the initial upslope and peak activity of the arterial blood samples described below.
Fresh frozen crops, ensiled crops (not frozen) and control samples (described below) were tested in triplicate.
In additional to the 24-hr duplicate food samples (described below), two spot urine samples and dietary consumption information were collected daily from all CPES children.
The target linguistic features (vocabulary, morphology, and syntax) were identified in academic discourse samples (described below) using Computerized Language Analysis (MacWhinney, 2000).
At each time point, DNA was extracted from the resulting cell pellet using QIAprep Spin Miniprep kits (Qiagen 27106) for PCR analysis (described below) and CFUs were counted for the day 7 samples (described below).
IAV infection prior to experiments was ruled out by blood serology (FlockCheck avian influenza virus antibody test kit; IDEXX, Hoofddorp, The Netherlands) performed at 10 weeks of age, and by real-time reverse transcriptase (RRT -PCR of the IAV matRRT -PCR frof fecal samples (described below) theen before the ducks entered the experIAVnt at 4 matrix of agene
This limited view of the input data is crucial, as many of the sampling approaches we describe below do not produce valid genome permutations (e.g., because of additional copies of adjacencies), yet still allow us to tally the number of linear chromosomes and of shared adjacencies.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com