So I totally slacked off today and went to lunch instead of writing the usual afternoon blog of the morning session, I hope you'll all forgive me, but to be fair those of you in the U.S. weren't even out of bed by the time lunch for me rolled around!
All of the presentations so far have been really awesome and informational so I hope you will take advantage of all the slides being posted on the website!
Today's morning session is great for PIs and students wishing to design sequencing experiments and determining to get an NGS platform.
I will be interjecting during this blog post...my interjections will be in a different color (probably green, because I like the color green).
Showing posts with label SOLiD. Show all posts
Showing posts with label SOLiD. Show all posts
Wednesday, January 9, 2013
Blog Series: WoG, Cesky Krumlov; Day 3: Genomics Study Design, a.k.a. "To seq or not to seq, that is the question!"
Labels:
454,
assembly,
ChIP-seq,
coverage,
depth,
evolution,
genomics,
Illumina,
metagenomics,
nanostring,
NGS,
PacBio,
PCR bias,
population,
quality,
reads,
RNA-seq,
Roche,
SOLiD,
Workshop on Genomics 2013
Tuesday, January 8, 2013
Blog Series: WoG, Cesky Krumlov; Day 2: So you want a NGS Sequencer eh?
Dr. Konrad Paszkiewicz
University of Exeter
Director of Wellcome Trust Biomedical Bioinformatics Hub
Topic: DNA Sequencing Technology: Past, present, future
Good morning bioinformatic campers! Well, afternoon for me, but morning for many of you back in the U.S.
So much of what was covered this morning is going to be redundant with the DNA sequencing preparation blog I wrote previously. So between this entry and that other one you will hopefully get a complete view of the 'state of the union' where sequencing is concerned and prospects for the future. The nice thing is that Konrad tossed in a lot of pro/con lists for different platforms, so those of you considering NGS in the future, this is a bare bones, get you started guide as to what's out there and whether 'it's worth it' for your own research to invest in a platform and which one to invest in. Again, I still highly recommend Dr. Elaine Mardis' talk that I linked in my DNA sequencing technology prep blog.
First and foremost, if you are familiar with what molecular biology is and what sequencing is and don't know who Fred Sanger is...then you've probably been living in a hole...
University of Exeter
Director of Wellcome Trust Biomedical Bioinformatics Hub
Topic: DNA Sequencing Technology: Past, present, future
Good morning bioinformatic campers! Well, afternoon for me, but morning for many of you back in the U.S.
So much of what was covered this morning is going to be redundant with the DNA sequencing preparation blog I wrote previously. So between this entry and that other one you will hopefully get a complete view of the 'state of the union' where sequencing is concerned and prospects for the future. The nice thing is that Konrad tossed in a lot of pro/con lists for different platforms, so those of you considering NGS in the future, this is a bare bones, get you started guide as to what's out there and whether 'it's worth it' for your own research to invest in a platform and which one to invest in. Again, I still highly recommend Dr. Elaine Mardis' talk that I linked in my DNA sequencing technology prep blog.
First and foremost, if you are familiar with what molecular biology is and what sequencing is and don't know who Fred Sanger is...then you've probably been living in a hole...
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