Unconfigured Ad

Collapse
This topic is closed.
X
X
 
  • Time
  • Show
Clear All
new posts
  • sramirez
    Junior Member
    • Oct 2010
    • 2

    #166
    Hi,

    I am an evolutionary biologist at UC Berkeley working on the re-sequencing of the Honey Bee genome for both population and pathogen analysis. I'm very pleased to have found this community, which already proved useful.

    Cheers!
    Santiago

    Comment

    • Dilipmohana
      Junior Member
      • Nov 2010
      • 2

      #167
      hi, dis is dilip and i am working as a bioinformatics analyst in chennai. I feel delighted to be a member here

      Comment

      • dmm
        Junior Member
        • Oct 2010
        • 1

        #168
        Hello to SEQanswers community

        Hello,

        I've recently started my postdoc at Harvard, and will be using RNA-Seq to look for mutations that cause congenital heart defects. I consider myself a developmental biologist, so stepping into the bioinformatics world is currently a stretch for me. I have spent a month reading many SEQanswers posts, and am excited to add my first post.

        Comment

        • dp05yk
          Member
          • Dec 2010
          • 66

          #169
          Hi,

          I'm a master's student from Canada and am working on writing an MPI version of BWA. I've read a bunch of posts from Heng Li and they have been helpful in my attempts to write this application. I am a computer science student first and foremost (I didn't even take biology in high school!) so this is all very new to me, but I'm loving getting into a new field.

          Comment

          • stoker
            Member
            • Oct 2010
            • 17

            #170
            Hallo!

            Bioinformatics PhD student from Gliwice, Poland here.
            Mainly interested in RNA Seq and R programming in cancer research.

            Tomasz
            Tomasz Stokowy
            www.sequencing.io.gliwice.pl

            Comment

            • plabaj
              Member
              • Oct 2010
              • 95

              #171
              Hi it seems that I overlooked this when I registered
              I'm PhD student (bioinformatics) at University of Life Sciences (BOKU) Vienna, Austria.
              Mainly interested in integration, managing and analysis of bioinformatics data.
              Recently playing with ABI SOLiD sequencing data.
              Pawel Labaj

              Comment

              • pland
                Junior Member
                • Dec 2010
                • 1

                #172
                Howdy

                I am a PhD student studying CNV in the lowly, (relatively) tractable fly. I hope to use deep sequencing to identify polymorphic variants that change gene structures or duplicate entire genes, and then use RNA-seq to see if these modified genes are expressed. We'll see.

                If anyone's actually reading this, and has their favorite study on anything related to these aims, by all means, let me know. Thanks.

                Comment

                • yinan0310265
                  Junior Member
                  • Dec 2010
                  • 1

                  #173
                  Hello everybody:
                  I am a PhD candidate of genomics, and presently I'm working in Saudi Arabia. I found this forum is a good community to exchange the experience and skills, so I would like to aquire some new konwledge from this group

                  Comment

                  • Rajendra
                    Junior Member
                    • Sep 2010
                    • 4

                    #174
                    Hi,
                    I work in IGIB as a research Assistant in India and working on NGS. I am glad to join this group and hope share my expertise and learn a lot from you all.

                    Comment

                    • gprakhar
                      Member
                      • Aug 2010
                      • 78

                      #175
                      Hi All,

                      I am a Bioinformatician, working in India's first Next Gen Sequencing Facility, GANIT Labs, Bangalore.
                      We have a Illumina GA IIx.
                      I am currently working on CNV detection in Cancer data and implementing Alignment algorithms on GPUs.

                      Comment

                      • Yepler
                        Member
                        • Oct 2010
                        • 22

                        #176
                        Hi all-

                        I'm a R&D scientist at a small company in Arizona - we're interested in using small RNA sequencing techniques and I've been lurking in the forums for a few months now. This is a super-helpful community; many thanks for keeping it up so well.

                        Comment

                        • aoler
                          Junior Member
                          • Apr 2010
                          • 3

                          #177
                          Hi all,

                          I am a Ph.D. student in oncological sciences. I use HTP sequencing for ChIP-seq, RNA-seq, and Bis-seq analysis. We have one GAII and one HiSeq Illumina machine at our institution. I use the forum for suggestions in analysis methods and looking for post-doc positions, and I hope to be able to help the community.

                          Thanks to all who contribute,

                          Andrew

                          Comment

                          • ashokpatowary
                            Junior Member
                            • Sep 2008
                            • 1

                            #178
                            GANIT labs being first NGS facility

                            Originally posted by gprakhar View Post
                            Hi All,

                            I am a Bioinformatician, working in India's first Next Gen Sequencing Facility, GANIT Labs, Bangalore.
                            We have a Illumina GA IIx.
                            I am currently working on CNV detection in Cancer data and implementing Alignment algorithms on GPUs.
                            Hi,
                            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...

                            Comment

                            • JennaLWoody
                              Junior Member
                              • Dec 2010
                              • 1

                              #179
                              Hi, My name is Jenna Woody from Iowa State University. I have not posted yet but this is a great resource! I have worked on transcriptome studies in Soybean using RNASeq and am now trying to do a de novo assembly with RNASeq in Phaseolus. Thanks for all of the help everyone!

                              Comment

                              • gprakhar
                                Member
                                • Aug 2010
                                • 78

                                #180
                                Originally posted by ashokpatowary View Post
                                Hi,
                                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...
                                Thank you and sorry if I was a bit ambiguous. GANIT Labs is a Public-Private initiative of DIT and Strand Life Sciences. I didn't mean to say that we are the first lab in India to do work on NGS or to have the first Next Gen sequencer, what i meant was, we are the first institute in India which works solely on NGS technologies.
                                We started in Oct'2010, hence you might not have heard about us.
                                and thanks again for the welcome.

                                Comment

                                Latest Articles

                                Collapse

                                • SEQadmin2
                                  Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                                  by SEQadmin2



                                  CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                                  Despite this, “CRISPR helped turn genome editing from a specialized technique into
                                  ...
                                  Today, 11:01 AM
                                • SEQadmin2
                                  Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                                  by SEQadmin2


                                  Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                                  The systematic characterization of the human proteome has
                                  ...
                                  07-20-2026, 11:48 AM
                                • SEQadmin2
                                  Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
                                  by SEQadmin2



                                  Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
                                  ...
                                  07-09-2026, 11:10 AM

                                ad_right_rmr

                                Collapse

                                News

                                Collapse

                                Topics Statistics Last Post
                                Started by SEQadmin2, Today, 02:55 AM
                                0 responses
                                7 views
                                0 reactions
                                Last Post SEQadmin2  
                                Started by SEQadmin2, 07-24-2026, 12:17 PM
                                0 responses
                                12 views
                                0 reactions
                                Last Post SEQadmin2  
                                Started by SEQadmin2, 07-23-2026, 11:41 AM
                                0 responses
                                12 views
                                0 reactions
                                Last Post SEQadmin2  
                                Started by SEQadmin2, 07-20-2026, 11:10 AM
                                0 responses
                                24 views
                                0 reactions
                                Last Post SEQadmin2  
                                Working...