BRN Discussion Ongoing

Would you prefer they read shareholder's questions or people who are looking at building products?
I'm not going to tell a 40 odd billion dollar business how to run their company.
Maybe email them and tell them they are going about this all wrong🤷‍♂️
 
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Boab

I wish I could paint like Vincent
Nope. I didn't delete any, but some sooks reported it.
I don't play victim, neither do I hide, I think we all know who's that famous for.

As to your "serve", @Quatrojos made a few pointers how someone entered and exited TSE along with LDA Ann timings, funnily enough April early was supposedly when LDA finished their deal. Haven't seen him since, have we?

Making this comment only because my posts here are frequently reported, and banned by the cartel, but I just wanted to say Hi to everyone.

Sean still has a couple of weeks to fulfill his "judge me on results" claim.
Can he bring home the bacon with an IP contract?
Or would he lean on all those immaterial partnerships to justify the oppies?

Also keen to see if he'll sell some of his free options like last year ? From memory it was more than $700k which he SOLD. How many will he sell this year, if at all? Surely if he sees this going places, he'd HODL it 😳 .


As to someone's concern me being a manipulator, company has my share holdings, and they can check if I'm trading this or not. I have no intentions here to mislead anyone, always dyor.
Plenty of us know you are not a manipulator, you just have opinions which may be different to others.
Cheers to you BL
 
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Slade

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I’m looking forward to Monday. It could be a good week ahead.
 
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MDhere

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I thought it might be interesting given Micro Morse dabbles in this general mmWave, radio signals area. Also, Michael De Mils (CEO Morse Micro) used to work in low-power digital IC design at Imec and Broadcom before founding Morse Micro.
and is in bed with Megachips:)
 
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MDhere

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I’m looking forward to Monday. It could be a good week ahead.
how many beers do u have lined up for next week?
 
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Tezza

Regular
After weeks of deliberations, I've decided to vote yes to bonus payments. Whilst I'm not happy with the sp, I am happy with the progress of the company and I am confident that we will have a better sp by the end of 2023. I will not vote yes next year if revenue is still low and unstable.
 
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D

Deleted member 118

Guest
Seems like things are moving along very nicely indeed



The data was analyzed by Brainchip with a Spiking Neural Network, the adjacent confusion matrix shows the results on the test set. The test set included 31 samples- 21 positives and 10 negatives from 21 tested subjects. Zero out of 21 positive samples were identified correctly which represents 100% sensitivity and 4 out of 10 negative samples were identified correctly which represents 40% specificity. The overall accuracy was 80.65% The second study was performed with the multiuse NaNose sensors installed in Sniffphone device. The dataset included 165 samples taken from 141 subjects tested with Sniffphone device at Zayed Military Hospital - 65 samples from 65 COVID-19 positive subjects and 100 samples from 76 COVID-19 negative subjects (Several negative subjects were sampled two or three times). A Linear discriminative analysis was performed. The adjacent confusion matrix shows the results on the test set that that was completely blind to the training and validation of the model. The test set included 37 samples - 8 positive and 29 negative samples from 27 tested subjects. Seven out of eight positive samples were identified correctly which represents 87.5% sensitivity, and 25 out of the 29 negative samples were identified correctly which represents 86.2% specificity. The overall accuracy was therefore 86.5%.
The same data set was analyzed also by the SNN methodology. To make the SNN most efficient, 34 samples were discarded due to noise or improper vector dimensionality. Thus, the dataset included 131 samples taken from 126 subjects tested with Sniffphone device at Zayed Military Hospital- 62 samples from 62 COVID-19 positive subjects and 69 samples from 64 COVID-19 negative subjects (Several negative subjects were sampled two or three times). The adjacent confusion matrix shows the results on the test set that that was completely blind to the training and validation of the model. The test set included 53 samples - 20 positive and 33 negative samples from 53 tested subjects. Nineteen out of 20 positive samples were identified correctly which represents 95% sensitivity and 29 out of 33 negative samples were identified correctly which represents 87.87 % specificity. The overall accuracy was therefore 90.5%.
Two different analysis methods were applied on the dataset and both showed excellent results for the differentiation between COVID positive and COVID negative. While the multiuse sensors achieved a much better specificity (-87%) compared to the single use sensors (40%), this is more likely a result of the vast difference between the datasets: the dataset of the multiuse sensors included 165 samples from 141 subjects while the dataset of the single-use sensors included 66 samples from 45 subjects. During the Clinical study with COVID19 patients the company further improved the 4 components of the device: the mechanical design including the breath collection mechanism, the electronics, the sensors and the classifying algorithm.
 
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Video won’t save separately but my unconscious bias says it’s a nod to Brainchip!
 
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alwaysgreen

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I’m looking forward to Monday. It could be a good week ahead.
@BaconLover

And this pie in the sky astrology post based on zero facts and a posters feelings is apparently worth keeping. 🤦🏽
 
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BaconLover

Founding Member
@BaconLover

And this pie in the sky astrology post based on zero facts and a posters feelings is apparently worth keeping. 🤦🏽
I've been seeing this prediction for a few months now.

Eventually it'll come true.

Be Here Now Clock GIF
 
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IloveLamp

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jtardif999

Regular
as
Seems like things are moving along very nicely indeed



The data was analyzed by Brainchip with a Spiking Neural Network, the adjacent confusion matrix shows the results on the test set. The test set included 31 samples- 21 positives and 10 negatives from 21 tested subjects. Zero out of 21 positive samples were identified correctly which represents 100% sensitivity and 4 out of 10 negative samples were identified correctly which represents 40% specificity. The overall accuracy was 80.65% The second study was performed with the multiuse NaNose sensors installed in Sniffphone device. The dataset included 165 samples taken from 141 subjects tested with Sniffphone device at Zayed Military Hospital - 65 samples from 65 COVID-19 positive subjects and 100 samples from 76 COVID-19 negative subjects (Several negative subjects were sampled two or three times). A Linear discriminative analysis was performed. The adjacent confusion matrix shows the results on the test set that that was completely blind to the training and validation of the model. The test set included 37 samples - 8 positive and 29 negative samples from 27 tested subjects. Seven out of eight positive samples were identified correctly which represents 87.5% sensitivity, and 25 out of the 29 negative samples were identified correctly which represents 86.2% specificity. The overall accuracy was therefore 86.5%.
The same data set was analyzed also by the SNN methodology. To make the SNN most efficient, 34 samples were discarded due to noise or improper vector dimensionality. Thus, the dataset included 131 samples taken from 126 subjects tested with Sniffphone device at Zayed Military Hospital- 62 samples from 62 COVID-19 positive subjects and 69 samples from 64 COVID-19 negative subjects (Several negative subjects were sampled two or three times). The adjacent confusion matrix shows the results on the test set that that was completely blind to the training and validation of the model. The test set included 53 samples - 20 positive and 33 negative samples from 53 tested subjects. Nineteen out of 20 positive samples were identified correctly which represents 95% sensitivity and 29 out of 33 negative samples were identified correctly which represents 87.87 % specificity. The overall accuracy was therefore 90.5%.
Two different analysis methods were applied on the dataset and both showed excellent results for the differentiation between COVID positive and COVID negative. While the multiuse sensors achieved a much better specificity (-87%) compared to the single use sensors (40%), this is more likely a result of the vast difference between the datasets: the dataset of the multiuse sensors included 165 samples from 141 subjects while the dataset of the single-use sensors included 66 samples from 45 subjects. During the Clinical study with COVID19 patients the company further improved the 4 components of the device: the mechanical design including the breath collection mechanism, the electronics, the sensors and the classifying algorithm.
Producing a patent for the device would suggest they (Nanose) are closer to realising a commercial product. I wonder how FDA approval is going? Could this be the start of real progress on the Nanose front?
 
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Slade

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What can I say. There are those that have done their research on BrainChip and remain quietly confident in the background happy with their investment. And then there are the ‘what’s a neuromorphic’ chip brigade.
 
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AusEire

Founding Member.
@BaconLover

And this pie in the sky astrology post based on zero facts and a posters feelings is apparently worth keeping. 🤦🏽
Did you report it? Or are you just going to tell us your feelings about it? 🤔🤷🏼‍♂️
 
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jtardif999

Regular
And are you sure you haven't been smoking the GREEN with your GREEN GINGER WINE? (Ha ha)🤪
Weed Party Hard GIF by reactionseditor
So that’s where FF has gotten to these days 🤓
 
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Diogenese

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Hi Tech,

Is the first BRN patent that does not name PvdM as an inventor?



View attachment 36340
Another odd thing about this patent application is that its priority date is 20220125. The normal publication date would have been 18 months after filing - 20230725.

There is a clue in the Accepted Journal Date, which is 20230511, the same as the Publication date.

This means that the application has undergone expedited examination by IPAU, the Australian Patent Office.

https://www.gestalt.law/insights/are-we-there-yet-expediting-examination-of-patents-in-australia#:~:text=It is possible to request expedited examination of,a granted patent by up to 10 months.

Expedited Examination

It is possible to request expedited examination of an Australian patent application in certain circumstances. If IPAustralia expedites examination it will issue a first examination report, or an acceptance notice, within 8 weeks of requesting examination. This can potentially shorten the time to obtain a granted patent by up to 10 months.

There are no additional official fees for requesting expedited examination. Under Regulation 3.17 the Commissioner of Patents has a discretion to grant a request to expedite examination if it is in the public interest or there are special circumstances that make it desirable. This is a fairly broad discretion that could include various types of circumstances.

IPAustralia’s Patent Examiner’s Manual provided in 2.13.4.3 that such circumstances may include:

a) the invention is in a field of technology that is environmentally beneficial (‘green’ technology);

b) the applicant is a small to medium sized enterprise (SME);

c) a valid request has been made under a Global Patent Prosecution Highway (GPPH) agreement; or

d) that there are pressing commercial reasons, such as the existence of

(i) a potential infringement or
(ii) a potential license or sale of the technology.
...
Green Technology

Otherwise, if the invention relates to a technology that saves on energy or materials or has an environmental benefit then this may also qualify.

Global Patent Prosecution Highway

If a corresponding patent application overseas has been examined and at least one claim has been found to be novel and inventive then this may provide a basis for a request under the GPPH
.



This is not an exhaustive list, and we know we meet a) and b), but let's hope the reason is not d)(i).
 
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