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  • 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!

    Comment


    • 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.

      Comment


      • 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 !!

        Comment


        • Originally posted by zun View Post
          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

          Comment


          • Originally posted by chrisaw01 View Post
            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

            Comment


            • 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!

              Comment


              • 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.

                Comment


                • 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!

                  Comment


                  • 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
                    --JaKaiser

                    Comment


                    • 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
                      --
                      Tirza Doniger, Ph.D.
                      Bioinformatics Unit
                      The Mina and Everard Faculty of Life Sciences
                      Bar Ilan University

                      Comment


                      • 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

                        Comment


                        • 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

                          Comment


                          • 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

                            Comment


                            • 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

                              Comment


                              • hi all,
                                I'm new to this forum, but it seems like a great place to find information relating to RNA-seq. Currently, I'm a PhD student using methods like Illumina sequencing of mRNAs to study cell fate determination in C. elegans. I'm looking forward to reading and learning on this site! -Mireille

                                Comment

                                Latest Articles

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                                • seqadmin
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                                  Next-generation sequencing (NGS) and quantitative polymerase chain reaction (qPCR) are essential techniques for investigating the genome, transcriptome, and epigenome. In many cases, choosing the appropriate technique is straightforward, but in others, it can be more challenging to determine the most effective option. A simple distinction is that smaller, more focused projects are typically better suited for qPCR, while larger, more complex datasets benefit from NGS. However,...
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