0:00:07 | my name is in line with the department of systems and computer engineering and my |
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0:00:14 | close to talk today is about what research with sensors champion sensors in the vitamins |
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0:00:20 | in palliative care to we looked at putting |
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0:00:23 | sensors into palliative care under the bed mattress is we put twenty four types of |
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0:00:27 | sensors in order to monitor people comfortably in a way that interfere with their comfort |
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0:00:33 | and we're of the first time we have our we had this study going where |
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0:00:37 | we have been able to monitor palliative care patients at the end |
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0:00:39 | the end of like what we found from that is that we can monitor how |
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0:00:44 | much they're in bad how much the rolling in bad and getting their respiration and |
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0:00:49 | breathing signals out from that we're looking at predictors of mortality and do we know |
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0:00:54 | can we tell interest rate |
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0:00:55 | operation signals that within the next couple weeks disparity field i and can we then |
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0:01:00 | be able to make better decisions are transferring them or not based on that are |
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0:01:07 | valuable spectrum part of computer engineering university |
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0:01:12 | and this is my thesis called towards personalised towards personalise interact tones |
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0:01:17 | and basically what that means is that when you're given and individuals are sequenced genome |
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0:01:23 | so their list of genes that they have in their body |
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0:01:26 | we wanna be able to predict the effects that and individuals mutations have on the |
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0:01:31 | protein interactions |
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0:01:36 | so the current bill this system we need a lot of input data so a |
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0:01:41 | lot of individuals sequence you know the test to test our system and to build |
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0:01:45 | our system |
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0:01:46 | and as a project called d thousand genome switch five sequenced and may be available |
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0:01:51 | a bunch of anonymous individuals sequence data |
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0:01:54 | and this told about how to twenty five terabytes |
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0:01:58 | which is pretty huge amount huge amount of data is we need to operate on |
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0:02:02 | this and identify candy mutations and things would like to test again some users as |
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0:02:08 | a as a system to build our |
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0:02:11 | our own system |
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0:02:13 | hi my name is alex the as and i am a graduate student at carleton |
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0:02:17 | currently studying statistics and i do the project on analysing national hockey league play by |
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0:02:22 | play data so the national hockey league keeps track of all sorts plays like a |
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0:02:26 | one during the game displays are defined the stuff like face off |
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0:02:29 | thoughts a periods beginning and ending shots shot blocks penalties goals and all that sort |
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0:02:34 | of and stuff and i decided this to take a look at some of the |
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0:02:36 | most important events and see what kind of information i could get out of it |
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0:02:40 | so when the big one big arguments right now in the n h l is |
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0:02:44 | whether or not we can measure |
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0:02:45 | measured success based on how long they possess about so the energy really tract this |
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0:02:50 | but luckily we can track shots or in shots against and there's pretty good relationship |
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0:02:55 | that says if you team takes more shots and i have shots against them then |
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0:02:58 | they probably have the pack more often and are probably more successful |
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0:03:01 | so this is essentially what i looked at and upon the relationship in general hold |
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0:03:05 | across the we got wraps up here and in them you can see that teams |
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0:03:09 | that have a higher percentage of the time ten to ten or more points over |
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0:03:13 | the course of the year and the teams or more points tend to get the |
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0:03:16 | playoffs and win championships |
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