[nhbach]

Hi everybody,

My name's Hoang Bach, I'm a doctor in Microbiology Department of College of Medicine and Pharmacy in Vietnam. I'm currently trying to study on genomic of Mycobacterium tuberculosis and i'm just getting started. Thanks to everybody who made this forum and who posted.

HBach

[cwhelan]

Hi Everyone,

I'm a PhD student in computer science and computational biology in the Biomedical Engineering department at Oregon Health & Science University (OHSU). I'm currently working on trying to detect structural variations and genomic rearrangements using Illumina mate pair data. Thanks to everyone who's already posted to the forums and made this such a great resource for someone like me who's just getting started.

Chris

[obig]

Hi all,

I'm a postdoc at Lawrence Berkeley National Laboratory. Before that I was at the Genome Sciences Centre in Vancouver. I've been working on RNAseq, ChIPseq, pathogen discovery and other analysis of (mostly) Illumina GAII data. I've been using this forum for a while but finally joining to start making contributions.

Obi

[Pawan Noel]

Hello Everybody,

I'm involved in a NGS project with Saccharomyces cerevisiae using the ABI SOLiD v4 system, so just wanted to say Hi and hope we can share problems and come to common solutions using this interface

Have a good day

Pawan

[tdoniger]

Hi

Hi,

I am work in the Bioinformatics Unit at Bar Ilan University,Israel. Most of our users have sequenced their data using illumina. I am fairly new to next generation sequencing and greatly appreciate stumbling across this forum.

Tirza Doniger

[JaKaiser]

Intro

Hi,

Im working with data Sequenced using Illumina's Cluster Station and GA2 with Paired-end Module and SCS v2.3, I've been interested in the process of taking the data from the image files through the workflow into a format for analysis. I have run into alot of issues and questions that Have been handled well by Illumina's Tech Support.

Im hear to learn from other peoples issues and maybe gain more understanding about NexGen Sequencing.

--JaKaiser

[El Mariachi]

Hello, everyone

I am a postgraduate in animal genetics and breeding. The subject I work on is about the copy number variations of domestic animals. The next generation sequecing provides the possibility for the detection of CNVs in the entire genome. Now I am still a newcomer in the field of high-throughput sequencing and I am here to learn.

Best wishes!

[uday_dd]

Hello All

Hi,
I am Uday Deshpande, working as a Professor Bioinformatics at Bharati University, Pune, India. Currently involved in developing Center of Excellence in Genomics and Proteomics. would like to share experience of next-gen seq data analysis. That why I am here.

[Mammon]

Hi all,

I'm a Master's student at the University of Manitoba, Canada. I'm in the department of Medical Microbiology, but I've been thrown into all this bioinformatics stuff! While I find it very interesting, it's also very overwhelming when it comes to the computer side of things. I only have very basic knowledge of HTML, C++, javascript and now I'm slowly learning Perl. I'll be posting lots of questions very soon!

[zun]

Hi Zun,

I also just started a RNA-seq project and would be interested to hear how things progress for you.

Chris

Hi, Chris
Thanks for reply

Wow,it seems difficult to define infectious desease genome
because there are so many mutations in it...

Now, I finished bowtie, tophat,cufflinks,cuffcompare to RNA-seq data.
Next, I am going to visualize the result with Gbrowse.

I am also interested in your study !
I am very happy to hear your progress if possible ;b

zun

[chrisaw01]

Hi, everyone

I just started analysing RNA-seq on my work.
This site is sooo helpful for beginners like me!

I am excited with discovering new genes or small RNA from NGS data!!

when I will ask some questions on this site,
please help me !!

Hi Zun,

I also just started a RNA-seq project and would be interested to hear how things progress for you.

Chris

[zun]

Hi! from Japan

Hi, everyone

I just started analysing RNA-seq on my work.
This site is sooo helpful for beginners like me!

I am excited with discovering new genes or small RNA from NGS data!!

when I will ask some questions on this site,
please help me !!

[chrisaw01]

Hello,

I am a Staff Scientist in a new genomics center for the U.S. Army. We using 454 and Illumina and our focus is on infectious disease genomics. I am pretty new to genomics and hoping to learn a lot from this forum.

[yangdu]

Hello!

I'm a Master's student studying autophagy expression in Drosophila.

I am new to this type of technology, but I am very fascinated with its capabilities and potential, and I hope to use the Illumina sequencing services to assist me in my thesis project

I'm very grateful for this online community!

[kalidaemon]

Hi everyone
I'm a postdoc in Boston. Working with both ChIP-Seq and RNA-Seq data to understand global differences in estrogen receptor binding and estrogen-mediated gene expression in cardiovascular tissue versus other tissues.