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Originally posted by hbn
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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
http://wasp.einstein.yu.edu/
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
http://genotypic.co.in/
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.
http://www.genewiz.com/public/complete_solution.aspxComment
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Amplicon sequencing is a targeted approach that allows researchers to investigate specific regions of the genome. This technique is routinely used in applications such as variant identification, clinical research, and infectious disease surveillance. The amplicon sequencing process begins by designing primers that flank the regions of interest. The DNA sequences are then amplified through PCR (typically multiplex PCR) to produce amplicons complementary to the targets. RNA targets...03-21-2023, 01:49 PM -
Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches...03-10-2023, 05:31 AM
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