Hello there,
Glad to be part of the community.
I am currently runing GNS core service in our SIgN (Singapore Immunology Networking - don't be misled, it is not a virtual organization, it is a immunology research institute with the size of 160 people) within Biomedical Science Institute, A*STAR, Singapore. I am helping the sicentists in immunology field to answer their biological questions using NGS technology. The facility is relatively new, it has only been up runing actively for less than a year.
Before relocating to Singapore, I was working for Illumina NGS product developing on sample prep kits (mRNA-seq, small RNA-seq......). Would be glad to help if someone out there have problem making libraries :-) as feeding the sequencer a good quality of library is essential.
Hope to learn more from your experience.
Best regards,
Wen
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Hello everyone,
I'm Khai from Malaysia. I'm doing research on WGS on colorectal cancer. I need help from you guys, how can i get the list of cancer genome that has been sequenced. I have a few papers but just wonder i might miss others. So if you know the full list of sequenced cancer genome, it would be appreciated to share it with me..
Thanks in advance
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wellcome,Margaret
Originally posted by margarettbry View PostHi, everyone,
I am a graduate student from Fudan University in China. One of my teachers recommended the Seqanswers forum. I found it every helpful for my starting to learn next generation sequence analysis.
Best!
Margaret
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Hi, everyone,
I am a graduate student from Fudan University in China. One of my teachers recommended the Seqanswers forum. I found it every helpful for my starting to learn next generation sequence analysis.
Best!
Margaret
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Greetings!
I am a postdoc working in germany and have just approached the next-gen sequencing technologies. I am performing ChIP-Seq studies by Illumina-Solexa.
I am glad this forum is up.
Cheers.
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Hello,
My name is Sérgio, I am currently doing a PostDoc at Embrapa in Brazil, working with Illumina and 454.
Cheers
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Hi,
My name is Avidya.I used to work on sample preparation of DNA sequencing for Illumina GA2 or HiSeq,and now I am interesting in the next-gen seq data analysis.Hope to help each other.
Avidya
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Hello!!
Hello!
I am a student in San Francisco currently trying to align Illumina reads to transposable element reference sequences. Nice to meet you all!
Jay
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Hi everybody.
I'm a student of the undergraduate program of genomic sciences in México. I'm starting working in the novo assembly and analisis of solexa reads data.
Greetings!
Fernando
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Hi
Hi everybody,
My name is Sayka Barry I am working at QMUL in London and planning to use next generation sequencing.
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Hi from Mathew
Hi I am from Australia and getting into sequencing. Excited to be here it is very well organized forum
BEst
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Hello
Hi,
I am a recent ms statistics grad. I am now a programmer working on RNA-seq at the ICNN at UCLA. I have found SEQanswers very useful. Thanks!
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Hi,
I'm a programmer working on whole chromosome visualizations across species. I'm here because I need some help understanding some of the surprises (for me, anyway) that I keep finding in the data.
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wassup to all!
happy new year gang!...to paraphrase the incomparable john lennon "lets hope it's a good one!"
I'm working in amsterdam as systems biologist in immunology and infection...i'll be trying to introduce the next gen seq techs especially the RNA seq (i believe the roche454 will be used; however i need to double check)...i'd first like to construct a library of pathogen (like strepto, staphylo, etc.) genome sequences for future reference...can anybody point me to the right direction? thanx in advance!
cheers and success to all!
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Originally posted by ashokpatowary View PostHi,
I am not sure,whether you are the first NGS facility in India,or it was IGIB(CSIR)
We have heard of Zebrafish genome sequencing and human genome sequencing fom IGIB long ago and never about GANIT labs.
Anyway...good luck and welcome to the community...
We started in Oct'2010, hence you might not have heard about us.
and thanks again for the welcome.
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