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Thread | Thread Starter | Forum | Replies | Last Post |
How to analyze RNA-seq data ? | bioR | RNA Sequencing | 3 | 09-12-2013 08:08 AM |
what is the best software to use to analyze illumina NGS data? | bbsinfo | Illumina/Solexa | 3 | 08-21-2013 05:48 AM |
DEXSeq - able to analyze paired (matched) data? | spabinger | RNA Sequencing | 13 | 02-08-2012 11:40 AM |
New Tools to analyze Next Gen Seq data | JMFA | Bioinformatics | 0 | 12-02-2010 09:26 AM |
any one use grape to analyze solexa data | zhidong | Bioinformatics | 11 | 05-22-2009 12:07 AM |
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#1 |
Member
Location: MI Join Date: May 2012
Posts: 11
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So imagine I have a FASTA file from my assembly run on the Miseq. As I am completely unfamiliar with anything to do with downstream analysis or the various software, I don't know what to do with the data. So...what's your favorite thing to do with it? What should I do? I assume I need to put all the reads together somehow. So please fill me with your knowledge oh wise ones!
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#2 |
Rick Westerman
Location: Purdue University, Indiana, USA Join Date: Jun 2008
Posts: 1,104
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ABySS.
But there are other genome sequencers as well. Some tuned to different branches of life; e.g., those oriented towards bacterial assembly. I suggest reading the forum. Lots of information in it. |
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#3 |
Member
Location: Raleigh, NC Join Date: Nov 2008
Posts: 51
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While redirecting it to /dev/null will save you alot of disk space and headaches, it may upset the PI.
Your question is much too vague. Define the purpose of the study then seek out tools. |
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#4 |
Senior Member
Location: Budapest Join Date: Mar 2010
Posts: 329
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Every analysis should be a goal and I choose programs that fits to it. What is your aim?
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#5 |
Super Moderator
Location: US Join Date: Nov 2009
Posts: 437
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A great suggestion especially for those that do not know why they did an experiment in the first place...
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#6 |
Member
Location: MI Join Date: May 2012
Posts: 11
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To be fair, I wasn't too sure of the goal myself. What we did was whole genome sequencing with a lot of genomes (E. coli, L. reuterii, and C. difficile). This was more of a trial thing to try out the MiSeq so there wasn't really a goal involved. Basically, I'm supposed to run it and play with the data to figure out what I can do with it.
I guess the questions are what is a good assembler for bacterial genomes? Right now I'm playing around with Velvet but I want to see what else is out there. So does anyone have any suggestions on what I could try out? Also, anyone a big fan of mapping and wanting to rave about their favorite program for it? |
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#8 |
Member
Location: Raleigh, NC Join Date: Nov 2008
Posts: 51
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Why don't you start with the MiSeq's onboard analysis tools (velvet, BWA, etc) , then move to the standalone version's of these to see what the increased ability to parameterize these tools can do for you, and then perhaps move on to other tools.
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