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The U.S. Nuclear Regulatory Commission (NRC) announced today that it has approved a final version of the Energy Infrastructure Technology (EIT) by Nucleus Software, Inc. The EIT is a unified software suite that provides tools to build and run nuclear power plants. It is a full-featured advanced computer application environment for modeling, planning, design, analysis and control of nuclear power plants and other advanced energy infrastructure, such as reactor designs, steam generators, pressurized water reactors (PWRs), BWRs, CANDUs, and sodium-cooled reactors. [Read more…]Q:

I need help debugging this Swift 2.0 statement

Its a very basic post, but I’m confused with this line of code.
let barriertag = self.barrier.tag

The error I’m getting is

“Use of unresolved identifier “barrier”

var tag = 0
func process() {
let barrier = NSTimer.scheduledTimerWithTimeInterval(self.animTime, target: self, selector: “TST”, userInfo: nil, repeats: true)
let tag = self.barrier.tag
println(tag)
}

A:

You need to add the self parameter to the closure:
let barrier = NSTimer.scheduledTimerWithTimeInterval(self.animTime, target: self, selector: “TST”, userInfo: nil, repeats: true)

You are calling the function with no parameter, so there is no value for the self parameter in the closure, hence the error.

President Trump’s pick to replace Jeff Sessions at the Department of Justice on Tuesday testified before the Senate Judiciary Committee about the need to ramp up anti-gang enforcement efforts.

Heather Mac Donald, a fellow at the Manhattan Institute, believes there are two main reasons why over 71 percent of children who are exposed to gang members will grow up to be gang members themselves

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A dose escalation study of weekly paclitaxel in combination with high-dose-rate intracavitary brachytherapy for cervical cancer.
To determine the maximum-tolerated dose of weekly paclitaxel in combination with high-dose-rate (HDR) intracavitary brachytherapy for treatment of locally advanced cervical cancer. The study design was an escalation dose-escalation phase I/II study. Nine patients with locally advanced cervical cancer were entered into four treatment groups: paclitaxel (Taxol, Bristol Myers Squibb Company) administered at a standard dose of 100 mg/m(2) on weeks 1 and 8 and HDR intracavitary brachytherapy administered on Mondays, Wednesdays, and Fridays. The HDR intracavitary brachytherapy doses were 24 Gy/4 fractions or 24 Gy/5 fractions plus a boost of 3 Gy to the primary tumor bed. Each group included one patient treated at a standard paclitaxel dose (100 mg/m(2)) and one patient treated at the maximum tolerated dose. The dose-limiting toxicity (DLT) was recorded as the maximum toxicity that occurred during the treatment or up to 60 days after its completion. The paclitaxel dose was escalated from 80 to 140 mg/m(2) weekly in 20 mg/m(2) increments. The maximum tolerated dose was found to be 130 mg/m(2). The main dose-limiting toxicity was grade 2 (16%), grade 3 (63%), or grade 4 (21%) neutropenia. Four patients (44%) experienced hematologic grade 3 toxicity. No patients had grade 3 or higher radiation toxicity. The maximum tolerated dose of paclitaxel in combination with concurrent weekly paclitaxel, and HDR brachytherapy administered on Mondays, Wednesdays, and Fridays
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