Does anybody know where I can get IonTorrent services performed?
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Ambry Genetics (http://ambrygen.com/) is the first authorized customer service provider for Ion Torrent sequencing.
Cheers,
Jason
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We can offer Ion Torrent services. I would be happy to provide more information! Feel free to send me an email with your information!
[email protected]
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in "Field guide to next-generation DNAsequencers" Glenn lists the minimum cost of an ion torrent run (a full 314 chip) at $750 ("Typical full cost (i.e. including labour, service contract, etc.) of the smallest generally available unit of purchase at an academic core laboratory
provider for the longest available read").
Anyone know where this? I'm not aware of any academic facilities offering ion torrent sequencing...
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I think this place does, but you'll have to confirm with them:
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For those offering services, what are generally the sample input req and deliverables? We have interest coming from the latest application note of 265 bp reads with better quality than the Illumina platform, but would like to see data generated on our samples.
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Looks like there is another one out there in Denmark:
It's an academic core facility.
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Service providers are starting to pop up all over the place. Now they are even specializing in a specific subset.
These guys:
... seem to be jumping on the ampliseq bandwagon and doing clinical applications. When I spoke with them, they mentioned BRCA and HNPCC. I just wish I had budget to get a system... so many ideas, so little time!
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Genomics Core at Children's Hospital Los Angeles
offers Ion Torrent sequencing, Affy expression and SNP arrays, NanoString panels
for pricing and sample requirements, please contact
Betty Schaub: [email protected]
Sherry Yen: [email protected]Scientific Data Analyst,
Center for Personalized Medicine
Children's Hospital Los Angeles
4650 Sunset Blvd
SRT1001A, MS#103
Los Angeles, CA 90027
USA
phone: 323-361-5842
email: [email protected] or [email protected]
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by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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Channel: Articles
07-01-2026, 11:43 AM -
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by SEQadmin2
I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
Here are nine questions we think about, in roughly the order they matter, before...-
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