Submitted by Anonymous on Sat, 23/04/2011 - 04:51.
So, is this life saying, for many performance metrics, that IT will not be competitive, and they have neither the vision or cranial horsepower to make it so. If that's the case, pathetic.
Submitted by Anonymous on Fri, 22/04/2011 - 23:34.
The Solvers ... have to agree that, upon submission, they grant Life Technologies non-exclusive, fully paid license to any and all intellectual property associated with the submission.
Got to love the fact that to submit an entry to the challenge, you have to grant LIFE a free and forever license to all the IP in your submission. And then nobody wins the $1,000,000...
Submitted by Anonymous on Fri, 22/04/2011 - 22:16.
re: read comment: ... I think that they can fix this in the next 6 months or so, and they are going to have to in order to stay competitive.
---
wow, global outsourcing R&D---
https://www.innocentive.com/ar/challenge/9932755
The Solvers ... have to agree that, upon submission, they grant Life Technologies non-exclusive, fully paid license to any and all intellectual property associated with the submission. The Winning Solver will assign exclusive ownership of all intellectual property to Life Technologies as per the terms of collecting the full award. This Challenge’s treatment of Solvers’ IP rights differs from a typical RTP Challenge, so read the Challenge Agreement (entitled Life Technologies’ Grand Challenge Terms and Conditions) carefully.
Submitted by Anonymous on Tue, 19/04/2011 - 16:03.
Man o man ! There is now two types of Life Tech rep, the good and the recyclable. The good are selling sequencers. I feel so bad for the legacy AB folks now on the gene ex side (or dark side)... ouch ! Nightmare ! I bet M.C. didn't explain that one when she said business as usual... What's going on at Ambion ? I don't see much coming out these days or is it in the usual Invitrogen destruction path.
Start your engine, they are looking at your run rate curves even before they calculated your new plan. If your post-yearly rate is not bad, you got another year to spare. If everyone around sucks, you will do some open coverage, work your ass off and then next year, as a reward, your manager will nix you of you are maxed out... even after a year of saving his ass. Ahhhh the beauty of a great system. Life Tech a great place to work !
Submitted by Anonymous on Mon, 18/04/2011 - 13:42.
Probably the usual middle manager who got nervous. Now he-she can say that he has an open territory to cover his back for lackluster numbers. An old Invitrogen trick. Ever seen a middle manager or a country manager pay for bad numbers ? The great leadership culture of Invitrogen. Funny how it's only one way.
Submitted by Anonymous on Sat, 16/04/2011 - 18:23.
I would like to say out here that they fired, in a cowardly fashion might I add, our local sales rep. A man who went through a lot for Invitrogen and a good rep. Can't believe it. I certainly will be looking at other media and enzyme vendors. How can a manager can do this ?
Submitted by Anonymous on Sat, 16/04/2011 - 02:06.
I would like to say out here that they fired, in a cowardly fashion might I add, our local sales rep. A man who went through a lot for Invitrogen and a good rep. Can't believe it. I certainly will be looking at other media and enzyme vendors. How can a manager can do this ?
Submitted by Anonymous on Thu, 14/04/2011 - 17:41.
read comment: I've seen some data from the Ion Torrent also (soon to be published). Quality and read length are certainly the most important area for them to improve, as the method (as of a month or two ago) was only getting about 67-long reads if you trimmed enough to get 1% error rates. The error rates shot up enormously towards the end of 100-long reads. I think that they can fix this in the next 6 months or so, and they are going to have to in order to stay competitive.
Submitted by Anonymous on Thu, 14/04/2011 - 08:09.
What's this about 60 base reads - I had a look at the Life website and could only find the press release - no technical information - do you have a link to where you saw this?
Submitted by Anonymous on Wed, 13/04/2011 - 18:38.
I'm impressed with the fact that it doesn't exist yet and that the machine still needs reads to be trimmed to around 60 bp to have any value. Isn't the spec at 100 bp ? Can I return my machine, whatÈs the rule on that ?
Submitted by Anonymous on Mon, 11/04/2011 - 23:09.
Coming on here to ask for reasonable feedback of a product is a shit idea. There is nothing but trolls and disgruntled folk here. You should ask a real discussion group about product feedback.
Submitted by Anonymous on Mon, 11/04/2011 - 22:59.
haha 36 samples a day, what are you talking about ? Who cares if your data is sh@t and the hands on time is a nightmare. You are perfect for Lifetech... Good luck with this... That machine is a nightmare and there are so many simple alternatives to it.
Submitted by Anonymous on Mon, 11/04/2011 - 17:18.
Is anyone buying the new BT/LT consumable. The Open Array gene expression for miRNAs? Is it good, useful? Have they made any improvements to the machine?
Submitted by Anonymous on Sun, 10/04/2011 - 05:03.
To all the high-fivers on Life Link Marketing Innovation who thought this partity was the cleverest thing ever...when LIFE actually comes up with a marketing campaign that has not already been run by Apple, or Google, or name any other internet/electronic company, THEN you can post it on "Marketing Innovation". If you are just copying other companies's sh!t, create a group for marketing rip offs and leave the innovation site to all the people that at least attempt to be original.
Life Tech is the Charlie Sheen of sequencing... WINNING!
Submitted by Anonymous on Sat, 09/04/2011 - 07:44.
"Illumina have been lying and taking low blows for years.
I'm pretty sure the last accuracy flyer i received from ILMN had solid 2 data on it...in 2011."
Maybe if someone could actually get published with a later SOLiD system ILMN wouldnL't have to use SOLiD 3 data.
Let's recap all the truth from ABI - SOLiD PI, Starlight, 300 Gb on SOLiD 4, PE reads, simplifying ePCR (if 900+ steps to 400+ steps is your idea of simplification), fractional use flowcells (well not really since you can only use them once)...lots of honesty flowing out of ABI there
Submitted by Anonymous on Sat, 09/04/2011 - 02:36.
What does that ignorant reply think sample prep is?
With every sequencer you have to make a library. For a useful sequencer (HiSeq, not SOLiD) that library can go into a cBot for automated amplification on the flowcell. Effectively having the cBot also sequence is the MiSeq. The user experience is golden. You can try and make automated bridge amplification into sequencing sound like a bad thing. It shows you have never run a next gen sequencer. You must also think people love the EZ bead over the cBot.
You consider sample prep post library creation? The PGM experience can be a nightmare. Let me make plates and plates of emulsions for my 28 runs. What is that, at least 14 full 96-well plates that I have to prepare, run on the 5 hour PCR cycle (3 days or 70 hours of just PCR) , then spend hours breaking the emulsions and doing enrichment? All that just to get beads to load into the sequencer. I'd rather pipet in my library, hit start and go do more productive than being a Life emulsion bead slave.
Ignorant is thinking anyone would prefer that over simply loading a library into the sequencer. So what it takes the machine longer to sequence? At least it does millions of reads to the PGM's tens of thousands of reads. Illumina sequencing is a known quantity. Data off the PGM has not been peer reviewed to substantiate their crazy claims and stupid marketing schemes.
Hmm, cure cancer with emPCR and Q17? Sure sounds ignorant to me. The PGM is just a crappy 454 with better marketing. Good luck.
Submitted by Anonymous on Sat, 09/04/2011 - 00:56.
The rereply is totally ignorant. Sample prep is locked up on the Miseq during the run. Library prep is totally separate, and libraries are cake. Nextera takes forever to optimize anyways. There are much more reliable automation systems out there.
The Ion will be cranking out GB runs multiple times a day while the MiSeq is churning for 27hrs.
Submitted by Anonymous on Sat, 09/04/2011 - 00:29.
My Life Tech rep said that if I bought two PGMs now and they didn't hit their promised spec in six months when the MiSeq came out, that Life would take back my PGMs. They are confident they will blow away Illumina with both read length, output, and huge improvements in sample preparation and I totally believe they will.
Submitted by Anonymous on Sat, 09/04/2011 - 00:16.
I think the sample prep issue comment is totally ignorant.
You can make libraries for both instruments in parallel. Use Nextera for the Miseq and it can happen in 30 minutes.
Either way you need to make libraries independent of the machine. For the MiSeq, I can pipette in that library and hit go. The instrument does automate the cluster generation and sequencing but it is one smooth step.
The PGM takes the same library, and you do emulsification, emPCR, break the emulsions, enrich, bead count, huzzah! you now can pipet a sample into the machine and hit go.
Saying the MiSeq is locked up and you can't prep samples is again a very ignorant thing a Life Technology rep would tell a customer.
Submitted by Anonymous on Fri, 08/04/2011 - 16:48.
Actually, it about time LT marketing grew some balls. Illumina have been lying and taking low blows for years. why not see what LT can come up with? I'm pretty sure the last accuracy flyer i received from ILMN had solid 2 data on it...in 2011.
Submitted by Anonymous on Fri, 08/04/2011 - 16:37.
Because the you can do the sample prep while the PGM machine is running. And you can prepare PGM samples in parallel. The MiSeq sample prep is locked up when it is running.
Submitted by Anonymous on Fri, 08/04/2011 - 13:24.
Illumina MiSeq runs without needing to do emPCR will all get done faster than PGM runs that each take days to prep. This ad with the two machines * two runs a day * 7 days = "28 runs per week" = a few weeks of sample prep. I wonder if they can also sell me a used car?
Submitted by Anonymous on Fri, 08/04/2011 - 07:02.
Interesting approach from Life, though I think this shows how desperate they are to get their machine out there before the (presumably higher quality) Illumina alternative hits the market.
The whole Apple vs PC angle doesn't really work though. Why do people buy the more expensive Apples instead of PCs? Because they are pleasurable to use and look and feel great.
On the other hand, the IT machine looks terrible, while the Miseq I saw at AGBT looked gorgeous, and should support a hugely more pleasurable user experience, if Ilumina's previous product offerings are anything to go by.
If Life are not careful, stuff like this ad, and GL going on TV saying that the IT can sequence whole chunks of your genome (actually a small fraction of 1% of your genome would be more accurate) are going to backfire on them badly.
Back in the day, Life had a decent reputation for quality instruments. All of the iterations of Solid sequencers which never quite cut it in terms of workflow or data throughput, despite their outlandish claims, have not laid a great foundation for this sort of marketing.
"Nice indeed. With revenue
"Nice indeed. With revenue increase percentage that is only 46 points smaller than ilmn."
Yes but Life has 4 times the revenue and much better EBITA
What happened to KM, Head of
What happened to KM, Head of Genetics Systems? Yet another one bites the dust!
Nice indeed. With revenue
Nice indeed. With revenue increase percentage that is only 46 points smaller than ilmn.
Nice quarter. Keep those
Nice quarter. Keep those stupid mid managers in sales and you're on your way to a steady decline. No question bout that.
Kind of bizarre that they can
Kind of bizarre that they can promise something that has yet to be delivered ?
So, is this life saying, for
So, is this life saying, for many performance metrics, that IT will not be competitive, and they have neither the vision or cranial horsepower to make it so. If that's the case, pathetic.
The Solvers ... have to agree
The Solvers ... have to agree that, upon submission, they grant Life Technologies non-exclusive, fully paid license to any and all intellectual property associated with the submission.
Got to love the fact that to submit an entry to the challenge, you have to grant LIFE a free and forever license to all the IP in your submission. And then nobody wins the $1,000,000...
re: read comment: ... I think
re: read comment: ... I think that they can fix this in the next 6 months or so, and they are going to have to in order to stay competitive.
---
wow, global outsourcing R&D---
https://www.innocentive.com/ar/challenge/9932755
The Solvers ... have to agree that, upon submission, they grant Life Technologies non-exclusive, fully paid license to any and all intellectual property associated with the submission. The Winning Solver will assign exclusive ownership of all intellectual property to Life Technologies as per the terms of collecting the full award. This Challenge’s treatment of Solvers’ IP rights differs from a typical RTP Challenge, so read the Challenge Agreement (entitled Life Technologies’ Grand Challenge Terms and Conditions) carefully.
Man o man ! There is now two
Man o man ! There is now two types of Life Tech rep, the good and the recyclable. The good are selling sequencers. I feel so bad for the legacy AB folks now on the gene ex side (or dark side)... ouch ! Nightmare ! I bet M.C. didn't explain that one when she said business as usual... What's going on at Ambion ? I don't see much coming out these days or is it in the usual Invitrogen destruction path.
Start your engine, they are looking at your run rate curves even before they calculated your new plan. If your post-yearly rate is not bad, you got another year to spare. If everyone around sucks, you will do some open coverage, work your ass off and then next year, as a reward, your manager will nix you of you are maxed out... even after a year of saving his ass. Ahhhh the beauty of a great system. Life Tech a great place to work !
Probably the usual middle
Probably the usual middle manager who got nervous. Now he-she can say that he has an open territory to cover his back for lackluster numbers. An old Invitrogen trick. Ever seen a middle manager or a country manager pay for bad numbers ? The great leadership culture of Invitrogen. Funny how it's only one way.
v What he said!
v What he said!
I would like to say out here
I would like to say out here that they fired, in a cowardly fashion might I add, our local sales rep. A man who went through a lot for Invitrogen and a good rep. Can't believe it. I certainly will be looking at other media and enzyme vendors. How can a manager can do this ?
So exactly why did you get fired?
which rep?
which rep?
I would like to say out here
I would like to say out here that they fired, in a cowardly fashion might I add, our local sales rep. A man who went through a lot for Invitrogen and a good rep. Can't believe it. I certainly will be looking at other media and enzyme vendors. How can a manager can do this ?
matrix management, with open
matrix management, with open eyes
http://www.youtube.com/watch?v=P01ZxSb3SZM
Eh? So how much does it
Eh?
So how much does it *actually* cost to do a run on an IT machine? By that I mean all in, library prep ePCR, reagents, chip etc.
And are any of these 1Gb Chios actually in the wild yet. If so, do they yield a Gb of data?
And what is the quality compared to the earlier chips?
by shot up, you must mean
by shot up, you must mean QV17 from QV20. How quite dramatic...
read comment: I've seen some
read comment: I've seen some data from the Ion Torrent also (soon to be published). Quality and read length are certainly the most important area for them to improve, as the method (as of a month or two ago) was only getting about 67-long reads if you trimmed enough to get 1% error rates. The error rates shot up enormously towards the end of 100-long reads. I think that they can fix this in the next 6 months or so, and they are going to have to in order to stay competitive.
http://omicsomics.blogspot.com/2011/04/better-template-prep-for-ion-anno...
He won't have a link because
He won't have a link because it's not true. The system already does trimming as well, so no one post trims even more.
What's this about 60 base
What's this about 60 base reads - I had a look at the Life website and could only find the press release - no technical information - do you have a link to where you saw this?
they are advertising it on
they are advertising it on the website, does anyone have plans to order a one touch sample prep machine???
I'm impressed with the fact
I'm impressed with the fact that it doesn't exist yet and that the machine still needs reads to be trimmed to around 60 bp to have any value. Isn't the spec at 100 bp ? Can I return my machine, whatÈs the rule on that ?
I'm impressed at claims for
I'm impressed at claims for the one touch sample prep for ion torrent....3 hours that's great...
GL doesnt have to sell to
GL doesnt have to sell to anyone but the shareholders.
Coming on here to ask for
Coming on here to ask for reasonable feedback of a product is a shit idea. There is nothing but trolls and disgruntled folk here. You should ask a real discussion group about product feedback.
LIFE'S a pissa That's for
LIFE'S a pissa
That's for sure
Working there?
Never a bore
But a family
Support you must
Not an employer
You can trust
Dr Doom
haha 36 samples a day, what
haha 36 samples a day, what are you talking about ? Who cares if your data is sh@t and the hands on time is a nightmare. You are perfect for Lifetech... Good luck with this... That machine is a nightmare and there are so many simple alternatives to it.
why? my manager wants to try
why? my manager wants to try it out since they are offering a really good deal on it 36 samples in one day...he wants me to try it.
That product is pure sh@t
That product is pure sh@t
Is anyone buying the new
Is anyone buying the new BT/LT consumable. The Open Array gene expression for miRNAs? Is it good, useful? Have they made any improvements to the machine?
I believe this is the worst
I believe this is the worst thread ever in the history of the rumor mill. Winning ? I think not.
To all the high-fivers on
To all the high-fivers on Life Link Marketing Innovation who thought this partity was the cleverest thing ever...when LIFE actually comes up with a marketing campaign that has not already been run by Apple, or Google, or name any other internet/electronic company, THEN you can post it on "Marketing Innovation". If you are just copying other companies's sh!t, create a group for marketing rip offs and leave the innovation site to all the people that at least attempt to be original.
Life Tech is the Charlie Sheen of sequencing... WINNING!
http://www.youtube.com/watch?v=GUr17pHezUo&feature=channel_video_title
Eat that Illumina!
"Illumina have been lying and
"Illumina have been lying and taking low blows for years.
I'm pretty sure the last accuracy flyer i received from ILMN had solid 2 data on it...in 2011."
Maybe if someone could actually get published with a later SOLiD system ILMN wouldnL't have to use SOLiD 3 data.
Let's recap all the truth from ABI - SOLiD PI, Starlight, 300 Gb on SOLiD 4, PE reads, simplifying ePCR (if 900+ steps to 400+ steps is your idea of simplification), fractional use flowcells (well not really since you can only use them once)...lots of honesty flowing out of ABI there
As an employee of LT, I know
As an employee of LT, I know that I would never purchase an LT product unless I have no other choice. They cannot be trusted.
What does that ignorant reply
What does that ignorant reply think sample prep is?
With every sequencer you have to make a library. For a useful sequencer (HiSeq, not SOLiD) that library can go into a cBot for automated amplification on the flowcell. Effectively having the cBot also sequence is the MiSeq. The user experience is golden. You can try and make automated bridge amplification into sequencing sound like a bad thing. It shows you have never run a next gen sequencer. You must also think people love the EZ bead over the cBot.
You consider sample prep post library creation? The PGM experience can be a nightmare. Let me make plates and plates of emulsions for my 28 runs. What is that, at least 14 full 96-well plates that I have to prepare, run on the 5 hour PCR cycle (3 days or 70 hours of just PCR) , then spend hours breaking the emulsions and doing enrichment? All that just to get beads to load into the sequencer. I'd rather pipet in my library, hit start and go do more productive than being a Life emulsion bead slave.
Ignorant is thinking anyone would prefer that over simply loading a library into the sequencer. So what it takes the machine longer to sequence? At least it does millions of reads to the PGM's tens of thousands of reads. Illumina sequencing is a known quantity. Data off the PGM has not been peer reviewed to substantiate their crazy claims and stupid marketing schemes.
Hmm, cure cancer with emPCR and Q17? Sure sounds ignorant to me. The PGM is just a crappy 454 with better marketing. Good luck.
I think the rep really wanted
I think the rep really wanted that Rolex in a bad way... How cheezy is that ?
The rereply is totally
The rereply is totally ignorant. Sample prep is locked up on the Miseq during the run. Library prep is totally separate, and libraries are cake. Nextera takes forever to optimize anyways. There are much more reliable automation systems out there.
The Ion will be cranking out GB runs multiple times a day while the MiSeq is churning for 27hrs.
My Life Tech rep said that if
My Life Tech rep said that if I bought two PGMs now and they didn't hit their promised spec in six months when the MiSeq came out, that Life would take back my PGMs. They are confident they will blow away Illumina with both read length, output, and huge improvements in sample preparation and I totally believe they will.
I think the sample prep issue
I think the sample prep issue comment is totally ignorant.
You can make libraries for both instruments in parallel. Use Nextera for the Miseq and it can happen in 30 minutes.
Either way you need to make libraries independent of the machine. For the MiSeq, I can pipette in that library and hit go. The instrument does automate the cluster generation and sequencing but it is one smooth step.
The PGM takes the same library, and you do emulsification, emPCR, break the emulsions, enrich, bead count, huzzah! you now can pipet a sample into the machine and hit go.
Saying the MiSeq is locked up and you can't prep samples is again a very ignorant thing a Life Technology rep would tell a customer.
Actually, it about time LT
Actually, it about time LT marketing grew some balls. Illumina have been lying and taking low blows for years. why not see what LT can come up with? I'm pretty sure the last accuracy flyer i received from ILMN had solid 2 data on it...in 2011.
Because the you can do the
Because the you can do the sample prep while the PGM machine is running. And you can prepare PGM samples in parallel. The MiSeq sample prep is locked up when it is running.
Illumina MiSeq runs without
Illumina MiSeq runs without needing to do emPCR will all get done faster than PGM runs that each take days to prep. This ad with the two machines * two runs a day * 7 days = "28 runs per week" = a few weeks of sample prep. I wonder if they can also sell me a used car?
Interesting approach from
Interesting approach from Life, though I think this shows how desperate they are to get their machine out there before the (presumably higher quality) Illumina alternative hits the market.
The whole Apple vs PC angle doesn't really work though. Why do people buy the more expensive Apples instead of PCs? Because they are pleasurable to use and look and feel great.
On the other hand, the IT machine looks terrible, while the Miseq I saw at AGBT looked gorgeous, and should support a hugely more pleasurable user experience, if Ilumina's previous product offerings are anything to go by.
If Life are not careful, stuff like this ad, and GL going on TV saying that the IT can sequence whole chunks of your genome (actually a small fraction of 1% of your genome would be more accurate) are going to backfire on them badly.
Back in the day, Life had a decent reputation for quality instruments. All of the iterations of Solid sequencers which never quite cut it in terms of workflow or data throughput, despite their outlandish claims, have not laid a great foundation for this sort of marketing.
Beware you don't look too desperate.......
Wow. Stay Classy Life Tech
Wow. Stay Classy Life Tech
Life Tech is the Charlie
Life Tech is the Charlie Sheen of sequencing... WINNING!
http://www.youtube.com/watch?v=GUr17pHezUo&feature=channel_video_title
Eat that Illumina!
http://news.morningstar.com/a
http://news.morningstar.com/all/business-wire/20110406005820/gnubio-make...
yes, more synergies and
yes, more synergies and consolidations are coming.
like I said. there is no
like I said. there is no move. get back to work.
What does Buba think of all
What does Buba think of all this:hogwash man !
http://www.lifetechnologies.com/news-gallery/news-and-views/photos/Greg-...
so are they moving FC ?
so are they moving FC ?
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