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| Thread | Thread Starter | Forum | Replies | Last Post |
| Roche Hostile bid for Illumina | rskr | General | 1 | 01-26-2012 07:39 AM |
| Looking for some statistics on Roche(454), Illumina & SOLiD platforms | Risha | Bioinformatics | 1 | 08-30-2010 06:20 AM |
| Looking for simple statistics on Roche(454), Illumina & SOLiD platforms | Risha | Introductions | 0 | 08-29-2010 02:05 PM |
| Roche 454 + Illumina/Solexa hybrid assembly strategies | RajAgainstTheMachine | Bioinformatics | 2 | 09-10-2009 11:23 AM |
| In Sequence: Illumina, Avantome, Roche, 454 Life Sciences, Applied Biosystems, InteRN | Newsbot! | Illumina/Solexa | 0 | 07-22-2008 01:06 PM |
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#1 |
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--Site Admin--
Location: SF Bay Area, CA, USA Join Date: Oct 2007
Posts: 1,248
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Roche is attempting a hostile takeover of Illumina...still absorbing this news...
http://www.forbes.com/sites/matthewh...dna-tech-race/ |
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#2 |
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Moderator
Location: Oslo, Norway Join Date: Nov 2008
Posts: 352
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Reactions on twitter seem to be very negative, echoing yours: "Let me be the first of many to say that I don't want Roche anywhere near illumina"
Would it mean the end of 454, and the start of the end for Illumina sequencing? |
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#3 |
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Senior Member
Location: Birmingham, UK Join Date: Jul 2009
Posts: 337
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Roche is a giant, with a market cap of $153.50bn vs $4.5bn for Illumina, so I guess they could make this happen if they really wanted to.
But in a way this news is strange because if Roche cares enough about the sequencing market to make an expensive hostile takeover bid for Illumina, why did they let the 454 technology stagnate for so long. Being a player in sequencing demands constant technological innovation. Perhaps they have learnt their lesson!? |
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#4 |
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Member
Location: Vienna Join Date: Feb 2010
Posts: 64
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Sounds like a bad idea considering that Illumina probably has reached its peak and their technology is strongly threatened to be made obsolete within the next 1-2 years (by IonTorrent).
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#5 |
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Senior Member
Location: Birmingham, UK Join Date: Jul 2009
Posts: 337
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This is why constant innovation is important. I don't believe Illumina are out of ideas just yet. Roche/454 seem to be though.
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#6 | |
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David Eccles (gringer)
Location: Wellington, New Zealand Join Date: May 2011
Posts: 289
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#7 | |
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Senior Member
Location: Birmingham, UK Join Date: Jul 2009
Posts: 337
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Quote:
Ion Torrent, 454, SOLiD and Illumina all require amplification of DNA to produce clonal molecular colonies for detection, but the first three technologies use bead-based emPCR whereas Illumina uses bridge amplification on a solid surface. Right now your choice for whole genome sequencing of humans is between Illumina and SOLiD. Proton should be a third option when released. 454 and PGM are suited for microbial-sized genome projects and amplicon sequencing. PacBio is good for specialised applications including eukaryotic de novo assembly and detection of nucleotide base modifications but doesn't directly compete with the others as doesn't have the throughput right now. |
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#8 | |
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David Eccles (gringer)
Location: Wellington, New Zealand Join Date: May 2011
Posts: 289
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#9 |
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Senior Member
Location: London Join Date: Jun 2009
Posts: 212
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Not many people know what Illumina have round the corner though. Details of the Oxford Nanopore collaboration is still sketchy.
Plus, Illumina still has some pretty useful IP that would be applicable to all the high throughput sequencing platforms. |
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#10 |
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Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 946
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As far as the US is concerned, the "clinical sequencing" market is probably the all important one. If Illumina is close to getting regulatory approval for sequencing of clinical samples then that could be the real reason of this takeover bid.
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#11 | |
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Member
Location: Vienna Join Date: Feb 2010
Posts: 64
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Quote:
As their technology relies on fancy optics and lasers it will always remain pretty expensive, slow and unreliable. They may offer the most bp per buck right now, but a clinical grade 1000$ or even 100$ genome using their current techology does not seem very realistic to me. |
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#12 |
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Member
Location: Alaska Join Date: Jan 2012
Posts: 47
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People need to serioulsy remove their research vision of sequencing, 100$, 1000$, 10000$ of buffer, chip and enzyme cost to sequencing have nothing to do witha proper clinical execution. There is a lot more involved in clinical worth than the simple part of sequencing... Anyone talking Solid or Pac Bio in a clinical study have not worked in the diagnostic field... There is SIMPLY no way this type sample prep can be automated under a 501K FDA let alone 21 CFR 11 software implementation (Ion Torrent also needs work there but much better IMO). There also needs to be a clinical worth... Need we talk about service and manufacturing demands of clinical requirements ?
May I remind everyone that Roche is the only player to manufacture drugs, manufacture diagnostic molecular instruments and have a basic research entity... Makes a lot of sense. Seriously, the cost of NGS could be zero $ today, there are still millions of dollars involved in proper clinical execution other than putting a drop on a chip... |
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#13 |
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Junior Member
Location: Cambridge, UK Join Date: Mar 2009
Posts: 6
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Roche have a history of overpaying for technology that, depending on you point of view is either at it's peak, or that they kill. I favor the later based on the rosetta inpharmatics, 454 and Nimblegen experiences. I suspect that Roche are too big and ungainly to be nimble as nothing seems to progress once they touch it.
SOLiD is dead, 454 is a Zombie, IonTorrent/Proton will not compete $/bp with Illumina, and PacBio is niche. The killer tech that Illumina have is clusters, it scales so much faster and better than emPCR - thats why IonTorrent can't win and will remain for smaller centers. That leaves nanopores, of which Oxford Nanopore is probably the leader, and Roche would be able to snag an interest in at least the Exonuclease sequencing version through Illumina - possibly killing both SBS and Nanopore. I hope this deal never happens. |
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#14 | |
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Senior Member
Location: London Join Date: Jun 2009
Posts: 212
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Quote:
It's the same with all technology (TV's, computers, mobile phones, sequencers, whatever) in that a basic model comes to market and then there are gradual improvements over time. However, you can only improve something so far before you need change the core technology (when it becomes available). This the reason why we're no longer running computers the size of rooms powered by valves, why we have nice flat screen TV's in our living rooms and why we can play Angry Birds on the way to work. |
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#15 | |
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Senior Member
Location: London Join Date: Jun 2009
Posts: 212
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#16 |
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Junior Member
Location: Cambridge, UK Join Date: Mar 2009
Posts: 6
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Hmm so so, I usually keep my glass topped up ;-)
So Tony what do you disagree with? I believe like you that Illumina has continued to execute improvements, borne out by the 1Gb>1Tb per run progression from GA>HiSeq. I haven't seen Roche manage anything similar nor would I expect them to start. I would however expect serious management changes, and I dont think that would be good. Initially, say 12-18months, it would be Ok, as Illumina have a lot of stuff in the pipeline that they can dish out when they want to e.g. when there is actually some competition. But as that runs out and the bets people leave...? |
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#17 |
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Member
Location: Vienna Join Date: Feb 2010
Posts: 64
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Dont think we disagree here. Illumina sequencing is awesome, has improved a great deal and is clearly the best choice for most applications right now!
All that I am saying is that its not 1000$ genome awsome and probably wont be in the forseable future. |
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#18 |
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Senior Member
Location: London Join Date: Jun 2009
Posts: 212
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I'm not saying it's a good thing either. I hope Illumina can remain out of the Roche's reach too.
It's taken Roche 4 years to go from 500bp to 700bp (and not too robustly if any of the XL posts on here are anything to go by). In the same time frame Illumina have increased their throughput approximately 1000 fold while a the same time driving down the costs. |
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#19 | |
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Member
Location: Vienna Join Date: Feb 2010
Posts: 64
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Quote:
Semi conductors are the killer tech here. They are much faster, scalable and so chap that you just trow your chip away after using it. Sure, we are not quite there yet. But you have to consider that Rothberg has kept all of his promises so far, shown us the machine and chips and will be shiping them to ealy access customers this spring. Ion Torrent will make the current illumina tech obsolete. |
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#20 | |
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Senior Member
Location: London Join Date: Jun 2009
Posts: 212
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Quote:
My experiences working in research is that the cost of sequencing is fine at the moment when using our Illumina machines. I'm not sure how many researchers would want to routinely do whole genomes as the analysis would be a bit challenging. About 10-15% of the cost of any project we undertake comprise of sequencing. The remainder are split between staff and sample prep. Bottom line: We need cheaper scientists and cheaper library prep kits! |
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