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Dear all,
another link from Italy
Lainate, Milan
GENOMNIA
http://www.genomnia.com/
(new web site in construction)
SOLiD
another link from Italy
Lainate, Milan
GENOMNIA
http://www.genomnia.com/
(new web site in construction)
SOLiD
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from NC
Duke University, Durham NC
454 GS FLX (with Titanium upgrade), Illumina Solexa GAII
http://www.genome.duke.edu/cores/sequencing/
UCSF Illumina GAII
http://genomics.ucsf.edu/Sequencing/index.aspxComment
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Please add NCGR to list of Next Gen Seq providers
Hi Eco,
This is indeed a great list. I just joined the group and started an intro thread.
Here are the pertinent details of our Next Gen Genome Sequencing center that I hope you can add to your spreadsheet:
0) Location: USA: Santa Fe, NM
1) Instruments: eight Illumina GAIIx's each with paired end modules
2) Analysis: One of a kind Computerworld awarded Alpheus analysis software for variant and expression detection.
3) Certification: We were the first Illumina CS-Pro certified provider in North America and have early acess to new Illumina technologies.
4) Support: We have a full time Illumina Engineer at our site to keep our instruments in top performance.
5) Website: http://sequencing.ncgr.org
Please contact me, Faye Schilkey, at [email protected] if you have any questions. Thanks, -FayeComment
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Hi
There is a new ABI SOLiD service provider for Asia Pacific.
They are based in Singapore.
http://www.aitbiotech.com/HTPSequencing.htm
Comment
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Genotypic, Bangalore, India (weblink: http://genotypic.co.in/)
Sequencing services from Genotypic: (454, Solexa, SoLiD)
Microbial re-sequencing, Transcriptome sequencing, Small RNA sequencing, ChIP sequencing, Bi-sulphite Sequencing, Whole genome sequencing and de-novo sequencing.
For more information: http://genotypic.co.in/new_gen.html?mnu=1Comment
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Service in Europe
IGA (Institute of Applied Genomics)
http://www.appliedgenomics.org/
Italy, Europe
Open to scientific collaborations and service provider: Illumina / Bioinformatics.Last edited by scalabrin; 08-02-2011, 11:27 PM.Comment
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Can you elaborate more on scientific collaborations?Comment
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Please make a new thread for this discussion! Thanks!Originally posted by kamichailo View PostComment
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Dear all,
the first SOLiD next gen sequencing Service provider in germany is settled in Tuebingen near Stuttgart and named CeGaT (Center for Genomics and Transcriptomics).
For further information please visit
http://www.cegat.de/
or contact
[email protected]
Kind regards,
CeGaTComment
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Hi,
a Germany based SOLiD service provider from Heidelberg:
http://www.febit.com/microarray-sequ...cing/overview/
contact:
[email protected]
devices:
2xSOLiD 3 plusComment
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Illumina GAIIx service in Vienna (Austria)
Dear all,
the University of Veterinary Medicine Vienna in Austria is offering sequencing service on an Illumina GAIIx (including paired-end module).
For further information, please send us an email to the address given at:
http://i122server.vu-wien.ac.at/pop/seq/VetCore2.htm
It would be nice, ECO, if you could add us to the "official" seqanswers list.
cheers
ViolaComment
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re Macrogen, Korea
Dear site administrator,
I'm now working for Macrogen in Korea and found that the site address "macrogen.com" can not redirect the user to our homepage. Please corerect the site to "www.macrogen.com".
Thank you,
Jongwoo SeoComment
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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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