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The Methods section begins with a description of the dataset preparation in Section 1 titled "Selection and Preparation of Datasets…".
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Discussion of natural polymers for hydrogel preparation in this section mainly has been limited to HA, chitosan, heparin, alginate, and fibrin, owing to scope of the article.
By introducing a new technique and utilizing preparations provided in Section 2, we will present an analytic expression of (p^{ast}(A,b)) such that every k-sparse vector x can be recovered via (l_{p} -minimization with (0< p< p^{ast}(A,b)) as l_{p} -minimizationecovered via (l_{0})-minimization.
In preparation section, Prepare Protein module in Discovery Studio 2.5 (DS 2.5) was employed to protonate the X-ray crystallography structure of TRAF6 protein with Chemistry at HARvard Macromolecular Mechanics (CHARMM) force field [ 39] and remove crystal water.
Mitochondrial preparations (prepared as described in section 'preparation and handling of mitochondria') were made 1% in CHAPS and the resulting solution was clarified by centrifugation at 14,000 rpm for 10 min. Whole-worm extract was prepared as described by [ 61].
For the sake of comparison, we initially run the algorithms without the preparation steps discussed in Section 3.4.
To generate more realistic results, we have also evaluated the three techniques including the dataset preparation steps presented in Section 3.4.
Detailed descriptions on dataset preparation are given in section " Data".
Further details of the sample preparation are given in section S5.
Consequently, a system's defocus must be avoided through sample preparation, as discussed in section 3. Since a dry MO is used with matched coverslips, we expect the tilt to introduce the main experimental aberration, apart from MO intrinsic aberrations.
We have generated NY-ESO-1 specific mAbs recognizing the target molecule in cytospin preparations and in sections from clinical tumour specimens.
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