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__TOC__
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== Setup ==
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<div class="mw-collapsible" style="width:600px">
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''If you are already logged in, you can skip this section.''
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<div class="mw-collapsible-content">
 
{{SeqShopLogin}}
 
{{SeqShopLogin}}
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</div>
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</div>
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== Setup your terminal ==
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Resume screen:
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screen -r
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   −
== Setup ==
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<div class="mw-collapsible mw-collapsed" style="width:700px">
''If you were sequenced, set these values:''
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'''Only if your snpcalling is still running, let Mary Kate know, expand, and follow these instructions'''
  export SAMPLE=Sample*
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<div class="mw-collapsible-content">
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* Detach from screen
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Ctrl-a d
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* Start new screen
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screen
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* Reset environment variables (replace SampleXX with your sample name)
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  export SAMPLE=SampleXX
 
  source /net/seqshop-server/home/mktrost/seqshop/setupSS.txt
 
  source /net/seqshop-server/home/mktrost/seqshop/setupSS.txt
source /net/seqshop-server/home/chaolong/LASER-Tutorial/setup.txt
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* When you detach from screen and reattach, you will have multiple screen sessions
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** The ancestry one will have today's date, the snpcall one will have an earlier date.
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*** Mary Kate can explain how to reattach to a specific session when we get there.
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</div>
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</div>
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'''Instructions for everyone: Setup LASER'''
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''If you were not sequenced, set these values:''
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Source the LASER setup:
export SAMPLE=NA12878
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source /net/seqshop-server/home/mktrost/seqshop/setupSS.txt
   
  source /net/seqshop-server/home/chaolong/LASER-Tutorial/setup.txt
 
  source /net/seqshop-server/home/chaolong/LASER-Tutorial/setup.txt
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(SAMPLE & OUT were previously set in your screen session.)
    
After setting this, also do
 
After setting this, also do
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This step takes ~1 hour for a genome sequenced at 17X.
 
This step takes ~1 hour for a genome sequenced at 17X.
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While this is running, we will go look at other results, so exit screen:
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Ctrl-a d
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While that's running, let's go run the Association Analysis Practical: [[SeqShop: Genetic Association Analysis Practical, December 2014]]
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=== Checking if Pileup finished ===
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screen -r
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'''Did everyone's finish?'''
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If not, let's go to Indel: [[SeqShop:_Calling_Your_Own_Genome,_December_2014#Reviewing_Indel_Results]]
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If yes, let's continue below:
 
=== Step 2: pileup --> seq ===
 
=== Step 2: pileup --> seq ===
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== Visualizing Ancestry ==
 
== Visualizing Ancestry ==
Copy the R code to plot your ancestry
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cp -r $LASER/plot/ $OUT/ancestry/.
      
Change to that new directory:
 
Change to that new directory:
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Take a look:
 
Take a look:
 
  evince Results_on_HGDP.pdf &
 
  evince Results_on_HGDP.pdf &
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== Return to Calling your own Genome ==
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Go to [[SeqShop:_Calling_Your_Own_Genome,_December_2014#Reviewing_Indel_Results]] and pick up where we left off.

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