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, 12:43, 12 December 2014
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| View the results: | | View the results: |
| less -S $OUT/ancestry/${SAMPLE}.HGDP.SeqPC.coord | | less -S $OUT/ancestry/${SAMPLE}.HGDP.SeqPC.coord |
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− | == Looking at Calling results ==
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− | If we haven't done INDEL: [[]]
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− | If we are moving on to SNPs: [[]]
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| == Visualizing Ancestry == | | == Visualizing Ancestry == |
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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/.
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| 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 == | | == Return to Calling your own Genome == |
− | Go to [[SeqShop: Calling Your Own Genome, December 2014#Friday:_Reviewing_SNPCALL_Results|Reviewing SNPCALL Results]] and pick up where we left off. | + | Go to [[SeqShop:_Calling_Your_Own_Genome,_December_2014#Reviewing_Indel_Results]] and pick up where we left off. |