Difference between revisions of "RNA Seq on HPC"

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[[ 9. Using bwa for read mapping and SNP calling ]]
 
[[ 9. Using bwa for read mapping and SNP calling ]]
  
[[ 9.1 Genome indexing for bra ]]
+
[[ 9.1 Genome indexing for bwa ]]
  
[[ 9.2 Read mapping using bra ]]
+
[[ 9.2 Read mapping using bwa ]]
  
 
[[ 9.3 SNP calling using varscan ]]
 
[[ 9.3 SNP calling using varscan ]]
  
 
[[ 10. Useful references ]]
 
[[ 10. Useful references ]]

Latest revision as of 15:32, 20 February 2016