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
Seqanswers Leaderboard Ad
Collapse
Announcement
Collapse
No announcement yet.
This topic is closed.
X
X
-
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
Leave a comment:
-
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
Leave a comment:
-
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
Leave a comment:
-
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.
Leave a comment:
-
Hello,
My name is Sérgio, I am currently doing a PostDoc at Embrapa in Brazil, working with Illumina and 454.
Cheers
Leave a comment:
-
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
Leave a comment:
-
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
Leave a comment:
-
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
Leave a comment:
-
Hi
Hi everybody,
My name is Sayka Barry I am working at QMUL in London and planning to use next generation sequencing.
Leave a comment:
-
Hi from Mathew
Hi I am from Australia and getting into sequencing. Excited to be here it is very well organized forum
BEst
Leave a comment:
-
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!
Leave a comment:
-
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.
Leave a comment:
-
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!
Leave a comment:
-
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.
Leave a comment:
Latest Articles
Collapse
-
by seqadmin
The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...-
Channel: Articles
04-22-2024, 07:01 AM -
-
by seqadmin
Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...-
Channel: Articles
04-04-2024, 04:25 PM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, Yesterday, 11:49 AM
|
0 responses
15 views
0 likes
|
Last Post
by seqadmin
Yesterday, 11:49 AM
|
||
Started by seqadmin, 04-24-2024, 08:47 AM
|
0 responses
16 views
0 likes
|
Last Post
by seqadmin
04-24-2024, 08:47 AM
|
||
Started by seqadmin, 04-11-2024, 12:08 PM
|
0 responses
62 views
0 likes
|
Last Post
by seqadmin
04-11-2024, 12:08 PM
|
||
Started by seqadmin, 04-10-2024, 10:19 PM
|
0 responses
60 views
0 likes
|
Last Post
by seqadmin
04-10-2024, 10:19 PM
|
Leave a comment: