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Originally posted by hbn
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Expression Analysis is now offering PacBio service!
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BMR Genomics, Italian leader for Sanger and NGS services now offers sequencing on
454 FLX
Illumina HiSeq 1000
SOLiD 5500 XL
and Bioinformatics Analysis services on NGS data.
For information please contact [email protected]
or visit : www.bmr-genomics.itComment
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Dear dottomarco,Originally posted by dottomarco View Post
to be honest I would say you are not the Italian leading company neither on Sanger nor on NGS sequencing. I apologize for the rude message but you are damaging IGA (Istituto di Genomica Applicata) and IGA-TS (IGA-Technology Services, that is IGA's commercial spin-off) with this post, see also http://seqanswers.com/forums/showpos...9&postcount=67Last edited by scalabrin; 08-05-2011, 12:51 AM.Comment
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Dear scalabrin <http://seqanswers.com/forums/member.php?u=4018>,
I am sorry for the misunderstanding and I thank you for pointing this out.
I din't intend to damage anyone; BMR Genomics is a private company and I was referring to this kind of subjects.
I know that in Italy there are many important genomic research centers that are also offering services.
Among these there is CRIBI Genomic Center that is where BMR Genomics was born 7 years ago and certainly there is IGA, that is well known and reputed.
But I'm sure you agree that the role and the aim of the two type of subjects is different.Comment
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I tried to access the Wiki to add one, but keep getting an Internal Server Error. Anyway, LC Sciences (http://www.lcsciences.com/) performs sequencing and data analysis. I've only used them for analysis but they have an Illumina system that we're planning on using in the future. We've only used the Houston, TX facilities but they have a China address listed as well, in Hangzhou.Comment
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University at Buffalo, The State University of New York
Next-Generation Sequencing and Expression Analysis Core Facility
Illumina HiSeq2000
Affymetrix GeneChip System
Roche 454 GS FLX Titanium
ubnextgencore.buffalo.eduComment
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Just wanted to update this thread to say that the wiki memory issues have hopefully been addressed, so if you had problems adding a tool or service lab please try it again!
Eric (and Dan who did most of the troubleshooting!
)
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Seems have to have been fixed, i was able to add our lab a bit earlier today! Thanks very much for hosting this list and site!Originally posted by ECO View PostJust wanted to update this thread to say that the wiki memory issues have hopefully been addressed, so if you had problems adding a tool or service lab please try it again!
Eric (and Dan who did most of the troubleshooting! )Comment
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Albert Einstein College of Medicine, New York
Illumina HiSeq 2000, MiSeq.
Primary data analysis included in cost.Comment
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Research and Testing Laboratory - Lubbock, TX
website: www.researchandtesting.com
email: [email protected]
454 FLX Titanium and Titanium Plus, Ion Torrent, Bio-Mark, LightCycler 480
Bioinformatics and BiostatisticsComment
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Genotypic Technologies (Bangalore, India)
Genotypic Technologies, Bangalore, India
Illumina GA IIx
Ion Torrent
SoLID
(454, HiSeq outsources)
AnalysisComment
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Next Generation Genomics at very low price INDIA Bangalore
Centre for Cellular and Molecular Platforms (C-CAMP), is a Dept. of Biotechnology (Govt. of India) initiative, and is a part of the Bangalore Bio-cluster. They currently have the following platforms:
* Imaging
* Flow Cytometry
* Next Generation Sequencing/Genomics
* High Throughput Screening
* Protein Technology Core
* Transgenic Fly Facility
* Molecular Characterisation Proteomics
Visit the Website www.ccamp.res.inComment
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GENEWIZ, the #1 provider of Sanger DNA sequencing services, now offers Next Generation Sequencing (NGS) services, as well as custom bioinformatics solutions. Operating with Illumina and Life Technologies platforms, GENEWIZ has capabilities to meet all of your NGS project needs.
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Love 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.07-01-2026, 11:43 AM
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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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