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  • JennaLWoody
    replied
    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!

    Leave a comment:


  • ashokpatowary
    replied
    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...

    Leave a comment:


  • aoler
    replied
    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

    Leave a comment:


  • Yepler
    replied
    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.

    Leave a comment:


  • gprakhar
    replied
    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.

    Leave a comment:


  • Rajendra
    replied
    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.

    Leave a comment:


  • yinan0310265
    replied
    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

    Leave a comment:


  • pland
    replied
    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.

    Leave a comment:


  • plabaj
    replied
    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.

    Leave a comment:


  • stoker
    replied
    Hallo!

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

    Tomasz

    Leave a comment:


  • dp05yk
    replied
    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.

    Leave a comment:


  • dmm
    replied
    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.

    Leave a comment:


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

    Leave a comment:


  • sramirez
    replied
    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

    Leave a comment:


  • ecofriendly
    replied
    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

    Leave a comment:

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