Sentence examples for in previous step from inspiring English sources
G. Value of bank in previous step.
The procedure is applied iteratively, calculating cost volume using the depth estimated in previous step.
It assumes the CoMatrix evaluated in previous step as input and returns an array of CoVs of size n, corresponding to (mathcal {D_{QID}}).
In this step, the result of road region in previous step is used to construct a training dataset from the corresponding regions of the satellite images.
As we know the absolute sign of inferior mode (known or estimated in previous step of estimation) and the estimated value of the pass function betwen modes and, we can find the absolute sign of mode.
If no result is achieved by the end, this repetition continues until Ñ = 2 indicates an error in this step of determining the number of subcarriers, or in previous step of determining the validity of the Gaussian tests.
(a) Beginning from the "ego" (here labeled 0), each successive identification step moves away from the current node, without any back-tracking to nodes in previous step-generations.
A mixture of 4,4′- 6,6′- 1,4-phenylene bis 2-aminopyrimidine-6,4-diyl))diphenol (0.01 mol) (synthesized in previous step-b) and 0.02 mol of substituted aldehyde was refluxed for 3–4,4′- 6,6′- 1,4-phenylene bis 2-aminopyrimidine-6,4-diyl
The solution of 3,3′- 1,4-phenylene bis 1- 4-nitrophenyl prop-2-en-1-one) (0.01 mol) (synthesized in previous step-i) in methanol (80 mL) was added with 0.01 mol of potassium hydroxide and 40 mL of 0.50 M solution of guanidine nitrate and refluxed for 5–6 h.
The solution of 3,3′- 1,4-phenylene bis 1- 4-hydroxyphenyl prop-2-en-1-one (0.01 mol) (synthesized in previous step-a) in methanol (80 mL) was added with 0.01 mol of potassium hydroxide and 40 mL of 0.50 M solution of guanidine hydrochloride and refluxed for 5–6 h.
In ethanol (30 mL), chloroacetyl chloride (0.02 mol) and 2 3 drops of triethylamine were added and the mixture was stirred in water bath for 10 min after that the solution of 6,6′- 1,4-phenylene bis(4-(4-nitrophenyl)pyrimidin-2-amine) (synthesized in previous step-ii) (0.01 mol) in ethanol (80 mL) was added drop wise and refluxed for 2–3 h.
