Hello Everyone,
I'm a graduate student working on a transcriptomics-based project and will be using Illumina and/or SOLiD platforms.
Cheers!
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hello, everyone. i am a graduate student and know very little about sequencing. i will often seek help here, and i hope you can be kind enough to help me, thank you.
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Hi all!
I'm a biologist (evolutionary genetics). I work at the Sequencing and Genotyping Facility located at the University of Puerto Rico. We're in the process of buying the Junior 454 from Roche and are waiting for the new Ion Torrent. If anyone has any good or bad comments about the Ion Torrent, they would be most welcome!
Cheers,
D.
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Hello to all,
I am just starting out by getting ready to crunch my first round of RNA-seq data off a GAIIx.
I am very excited and I am becoming increasingly grateful to the creators of this forum. I have already learned a good deal.
The following is a primer on PERL for biologists from one of my professors, Dr. Korf: http://korflab.ucdavis.edu/Unix_and_Perl/index.html
I found it very useful.
See you guys around..
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Hello everybody,
I am a postdoc working on RNAseq; my data come from Illumina genome analyzer II SCS2.6. Glad to have found this forum.
Cheers
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Hi everyone,
This forum is awesome. We are just beginning to provide Illumina sequencing services as part of our Genomics Sequencing and Microarray Core at Cincinnati.
sai
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Hello~
I am a new Ph.D. student in UQ, working on deep-sequecing data.
Thanks for SeQanswers, I find our group.
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Hi
Hello All,
I am Uday Evani from Houston. i am bioinformatician who has just entered this field. Currently i am working on ways to improve a home grown indel calling pipeline. i have found seqanswers to be very useful resource and has helped me a lot in getting to know the field. very excited to be here and see you around.
Uday
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Hello, everybody
I am a graduate student on biology, and working in BGI. Glad to come here and learn from you all.
Cheers!
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Hello there,
My name is Chun-Nan and I'm based in San Jose, California, US. I'm working on exploring the "immunome" by next gen sequencing. Because of the read length consideration, I'm heavily leaning toward using 454 technology.
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Hi all,
I'm Malachi, a postdoc at the Genome Sciences Centre, BC Cancer Agency. I just completed my PhD in medical genetics. I have spent the last ~2 years analyzing RNA-Seq data in the context of alternative splicing.
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Hi folks,
This is Da. I am a postdoc in MD Anderson Cancer Center. Although I deem myself as a bioinformatician, my previous experience was limited on the microarray analysis using R. I am pretty new in NGS, nice to meet you here.
Da
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Hello
Hello Next Gen Seq community!
I'm Mikaela from Partek, we do bioinformatics software for statistical analysis of next gen seq and microarray data - with a focus on biological exploration of results.
My job is to plan data analysis trainings/seminars/webinars, helping scientists getting started with their own datasets.
We're genuinely interested in offering support and to interact and discuss about the methods available for RNA-Seq, ChIP-Seq, Methyl-Seq, DNA-Seq and Functional Genomics.
I really enjoy reading the posts on seqanswers!
You are welcome to contact me at [email protected]
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som san
dear som san
nice to hear that. I am now in fujiwara sense s lab, doing some chip as a collaborative student from india. nice to meet you here. i am returning to india in next week. will keep in touch with you. pls send a mail at [email protected].
arigato
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