Also - if you build your array in an object it might automatically cache for the life of that httpd server, but I'd have to look it up. When you start the server you can fill in an array within an object and make it available to all the threaded or child httpd processes since it doesn't really change until you add more photo's
Glad you got it working. You could also just write the file list out to a single file, and recreate it once a month or so. Then the load process would just have to read in that one file to get the image list, rather than scanning the entire directory tree. Dave
That deserves one of my robot like psychobabble responses but that already turned out bad once today. Ruben
Dave - I could... but then no, i cant while i was able to take the code you provided and tweak it to work within what i wanted it to do... there is no chance of me writing original code. I even copy code directly from the book on php that i am reading... the book says it works, but yet when i do it, it doesnt lol Ruben .. i never doubted what you have said was right lol But i cant write original code. I can take a prewritten code and play with it to make it work for me. but thats it. And even then it has to be simple stright forward code. You might have said 4 pages ago a tactic to try, but it went way over my head then, and is flying way over my head now
You need to practice on your own server http://en.opensuse.org/Live_CD http://en.opensuse.org/Live_USB_stick I have no doubt you can master these skills. Ruben
You guys are making my head spin with all the programming talk! Lets talk cell cultures and I can keep up with ya!!! LOL... I am about to embark on an HTML course myself..it's about time!! RickieB
I actually can talk cell cultures if you want Aerobic or Anaerobic Bacteria? C. Difficile, H Influenza, ,Helicobacter pylori, Klebsiella pneumoniae, Pseudomonas Aginiosis, Acinetobacter calcoaceticus, Moraxella catarrhalis, Neisseria meningitidis, Legionella pneumophilia, Enterobacter cloacae or a half dozen Step or Staph strains? One of the great things about my Pharmacy education is that it is very very broad. Everyone should learn basic HTML so I commend you on that. Next time we talk, lets converse about Taylor Polynumerials series and Lamda Calculus and irrational number theory. Ruben
Ruben...all those that you mentioned are microbial species and are refered to as fermentations.... (these days they are broken up into two groups) cell culture and fermentation, although the meanings are basically the same. I do quite a bit of that as well, also starting to work on fermentations for biofuels...but my main background is in the process development side of mammialian cell cultures for rDNA therapies and vaccine development. I left the Lab long ago, but still try to keep up. These days I am working with the system that grow them (in-vitro) and thus provide the vehicle for modern day new drug therapies that you provide through the pharma industry. Anytime you wanna chat..let me know... RickieB
Actually the rDNA therapies and the ability to grow them in broths is an exciting breakthrough and it is going to have major impact in the near future. You were telling me about them before and you opened up my eyes to how this is currently developing. There are catches though. I went to San Fransisco last year for a weeks worth of meetings and work shops on recombinant anti-bodies and biological developments. The trouble they run into, and this is critical for dosage delivery systems, is that these very biological active compounds are also highly antigenic by design. They are functioning right there at the level of immunological activation and they already had one very very bad clinical trial. Our technology might just not be there yet because to avoid this kind of problem within realistic and practical levels of safety, it might be necessary to build a cocktail mapped directly to the immunological conditions of the patients and rDNA fermentation might go a long way towards that. But there are a lot of hurdles to leap over, not the least of which is that a normal drug is tested on 500 patients in primary clinical trials, and thousands of patients in secondary trials before being released. Here what we are proposing is that each batch is a new and different delivery system going to the patient without ANY trials, and once those slow releasing intracellular mediators get released into the blood stream, all a MD can do is supportive medicine and watch the results with horror. Ruben
I am with you!!!! RickieB ... it might make Rubens head spin a bit (which truly is a bit of fun to watch lol) but i got a hold of these lessons by the Video Proffessor ... the cd's go into alot of detail in covering the basics of html coding. Along the way, you sent up a website as you learn, and it covers creating tables, posting image, hotspoting links and a whole lot more. It only coveres the basics, but it was really great! Let me know if your interested and ill send you my cd's
Your right. The Video Professor does make my head spin. He's just terrible. Really, pick up a decent book and just go through it. However, the harder part is learning how to use a decent text editor (not word processor). Look up VIM and learn it first. It is your tool for all other coding. Trust me on this. I've had substantial programming teams I've worked with and eventually everyone converts to GVIM except for a few EMACS hold outs. http://www.vim.org/ Ruben
Roman fortificains is a terrific topic that I have only the slimmist knowledge of. Where do we start? Ruben