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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
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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
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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.
Peer-reviewed, open access journals for science, technology, social science and medicine. Indexed in the leading abstracting and indexing databases.
fengfeng
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Hey, all
A bioinformaticain working on microbial genomics and comparative genomics.
W
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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
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Greeting
Hi Everyone,
I'm going to work with NGS data,so excited to find this great community.
Best
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Greetings from Germany
Hi all,
I am a bioinformatician from Düsseldorf, working on 454 and solexa paired-end reads.
Cheers
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Hi all,
I am a technician in Heidelberg working on solexa single end & PE and RNA seq
gg
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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.
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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
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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.
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Hi all,
I'm a research fellow at the Baker Heart institute in Melbourne using the GAIIx to study epigenetics and transcriptomics.
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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
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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
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Hello everyone!
I am a PhD student at the Technion, Israel Institute of Technology. Usually working on metagenomics, but in the coming few months will be working on Solexa data.
Cheers,
Itai
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Technological advances have led to drastic improvements in the field of precision medicine, enabling more personalized approaches to treatment. This article explores four leading groups that are overcoming many of the challenges of genomic profiling and precision medicine through their innovative platforms and technologies.
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The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...-
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