Unconfigured Ad

Collapse
This topic is closed.
X
X
 
  • Time
  • Show
Clear All
new posts
  • jww
    Junior Member
    • Mar 2010
    • 1

    #76
    greetings from ca

    Hi All,
    Thanks for this great forum. Found some useful stuff already.
    I'm a 4th year grad student at Stanford. Interested in sequencing novel and/or evolved yeast genomes on Illumina...
    Best,
    jared

    Comment

    • mhampton
      Junior Member
      • Oct 2009
      • 4

      #77
      Hi,
      I am a mathematician at the University of Minnesota, Duluth. I will soon help some biologists analyze transcriptome data for the 13-lined ground squirrel, a small mammalian hibernator, using a 454 sequencer. The ground squirrel has a 2X coverage WGS data, I'll be trying to figure out how to leverage that.
      -M. Hampton

      Comment

      • markz
        Junior Member
        • Mar 2010
        • 1

        #78
        Hi all,

        I'm a research fellow at the Baker Heart institute in Melbourne using the GAIIx to study epigenetics and transcriptomics.

        Comment

        • saha
          Junior Member
          • Jan 2010
          • 5

          #79
          hello i am Saurav. I am a newbie to seqanswers. i was just searching for where to start and found this page. i am basically working on applied biosystem's SOLiD platform. I am new to high throughput sequencing.

          Comment

          • Linnea
            Member
            • Mar 2010
            • 23

            #80
            Greetings from Uppsala

            Hi!

            I am a recently graduated bioinformatician and have just started working as a research engineer. I am trying to de novo assembly transcriptome Solexa sequences but am a newbie to this by all means! This seems to be a great forum though!

            Cheers,
            Linnéa

            Comment

            • jeny
              Member
              • Mar 2010
              • 16

              #81
              Hi all,

              I am a bioinformatician and I started to work on illumina GAiix last week.
              I will have in charge : data storage, software tests, and data analysis.
              I think this forum will be helpfull !

              Cheers.

              Comment

              • gogreen
                Member
                • Apr 2009
                • 18

                #82
                Hi all,
                I am a technician in Heidelberg working on solexa single end & PE and RNA seq
                gg

                Comment

                • SingleCell
                  Junior Member
                  • Mar 2010
                  • 1

                  #83
                  Greetings from Germany

                  Hi all,

                  I am a bioinformatician from Düsseldorf, working on 454 and solexa paired-end reads.

                  Cheers

                  Comment

                  • xuewei
                    Junior Member
                    • Mar 2010
                    • 1

                    #84
                    Greeting

                    Hi Everyone,

                    I'm going to work with NGS data,so excited to find this great community.

                    Best

                    Comment

                    • lakshmi
                      Junior Member
                      • Mar 2010
                      • 1

                      #85
                      Hi from Boston

                      Hello!

                      I am a physicist making a transition to Bioinformatics- I find this field exciting! Currently working with ChIP-seq data. Looking forward to interesting discussions!

                      Cheers,

                      Lakshmi

                      Comment

                      • biomed
                        Junior Member
                        • Dec 2009
                        • 6

                        #86
                        Hey, all

                        A bioinformaticain working on microbial genomics and comparative genomics.

                        W

                        Comment

                        • cdragon
                          Professor of Health Informatic
                          • Jan 2010
                          • 12

                          #87
                          My self introduction

                          Hi All,

                          I'm Fengfeng Zhou, an assistant research scientist from the University of Georgia, Athens, Georgia, USA. I'm working on sequence based comparative analysis of mobile genetic elements and how they contribute to the evolution of the host genomes. You may find my details at my personal web page:



                          btw, you are welcome to submit your next manuscripts to the journal Sequencing.

                          http://www.hindawi.com/journals/seq/

                          fengfeng
                          Website: http://www.fengfengzhou.org/FengfengZhou/

                          Comment

                          • ulz_peter
                            Senior Member
                            • Feb 2010
                            • 219

                            #88
                            It's me

                            Hi guys,

                            I'm lab technician studying bioinformatics in Graz while working at the Institute of Human Genetics in Graz / Austria (Mozart, no Kangaroos). Two more weeks until we get a FLX System...
                            Prepare yourself for many many questions

                            Comment

                            • shabhonam
                              Junior Member
                              • Apr 2010
                              • 4

                              #89
                              Hi My name is Shabhonam Caim, I work at The Genome Analysis Centre, UK. I am currently working on solexa and 454 data. I hope to get and provide help here

                              Comment

                              • richardbadge
                                Junior Member
                                • Apr 2010
                                • 3

                                #90
                                Hi All,

                                I am an academic in Leicester, UK with growing interests in using HTS systems for studying high copy number repeats in mammalian genomes (OK I know that sounds crazy / masochistic).

                                We are getting ready for our first 454 experiment, but I'm interested in data analysis for all the major systems (my other hat is co-convenor of an MSc in Bioinformatics course!)

                                Great idea to gather a community!

                                Richard

                                Comment

                                Latest Articles

                                Collapse

                                • SEQadmin2
                                  Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                                  by SEQadmin2



                                  Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                                  Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                                  ...
                                  10-14-2026, 09:55 AM
                                • SEQadmin2
                                  New Genomics Technologies Take Aim at Long-Standing Limits
                                  by SEQadmin2


                                  Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

                                  We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
                                  ...
                                  09-28-2026, 10:25 AM

                                ad_right_rmr

                                Collapse

                                News

                                Collapse

                                Topics Statistics Last Post
                                Started by SEQadmin2, 10-15-2026, 10:52 AM
                                0 responses
                                14 views
                                0 reactions
                                Last Post SEQadmin2  
                                Started by SEQadmin2, 10-14-2026, 05:39 AM
                                0 responses
                                21 views
                                0 reactions
                                Last Post SEQadmin2  
                                Started by SEQadmin2, 10-13-2026, 09:56 AM
                                0 responses
                                19 views
                                0 reactions
                                Last Post SEQadmin2  
                                Started by SEQadmin2, 10-09-2026, 11:14 AM
                                0 responses
                                27 views
                                0 reactions
                                Last Post SEQadmin2  
                                Working...