Sentence examples for acc I from inspiring English sources

Individuals with a high learning rate within ACC (i.e. learning from errors, adapting the following behavior to circumvent unwanted consequences in future) resemble the known patterns of the model: the higher the probability to commit an error the higher the activity within ACC.

If a prediction method yields high ACC i with small i and low ACC i with large i, it is deemed as an effective prediction.

It is obvious that ACC i is the ratio of correct ith order predicted samples to all samples.

The ACC for node i is defined as (1) ACC i = 2 C i d i (d i − 1 ).

G-mean computes the geometric mean of all classes' accuracies and is described as follows: (14) G -mean = (∏ i = 1 C Ac c i ) 1 / C, where Acc i denotes the accuracy of the ith class.

To evaluate the correctness of the candidate indication, the ith order prediction accuracy was calculated by (6) ACC i = P D i N,   i = 1, 2, …, 56, where N denoted the total number of samples, while PD i denoted the number of samples whose ith order prediction is correct.

A full-length NF-L-myc tagged construct [16] was digested with Nde I- Acc 65 I 1-3699 acids andds), aNdeNde I- Bgl II (1 243) was end filled and ligated in frame with the C-terminal Myc-tagged pET11a expression construct (Novagen, Gibbstown, NJ).

Based on the polymorphism at the splicing site of the first intron, a co-dominant CAPS (cleaved amplified polymorphic sequence) molecular marker PCR-Acc I was developed for selection of Wx alleles in rice breeding (Cai et al. [2002]).

The amplified products were electrophoretically resolved on a 1.5% agarose gel for marker sd1STS, a 2.0% agarose gel for marker 21, and a 3.5% agarose gel for marker PCR-Acc I and RM224 in 1 × TAE buffer.

Template DNA was initially denatured at 94°C for 2 min followed by 35 cycles of PCR amplification with the following parameters: a 30 s of denaturation at 94°C, a 40 s of primer annealing at 55°C for markers 21, RM224 and PCR-Acc I, 65°C for maker sd1STS, and 1 min of primer extension at 72°C for markers RM224 and PCR-Acc I, and 1.5 min for markers 21 and sd1STS.

For pAP2-HA-Red, the NgoAIV-AccI fragment from pRIG-HA-Red was cloned into BBg (a derivative of pBluescript SKII containing a BglII site) digested with XmaI-AccI to give the BBg HA-Red from which the BglII -XhoI fragment (coding for the HA-DsRed fusion polypeptide) was purified and recloned into the pAP2-IRESeGFP vector opened by BglII and XhoI.