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#1 |
Member
Location: chicago Join Date: Nov 2012
Posts: 19
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Hi,all
I am doing RNA-seq alignment with STAR, my workstation is dual core(E5-2620v3), 12 thread in total, 64G RAM. I am running 9 mouse RNA-seq sample data(1GB/sample), parallelly, two days has gone, still no result. No error, the log just say start mapping. Can any one with similar experience tell me how can I make it faster or is there anything wrong. Below is my command: /STAR-STAR_2.4.2a/bin/Linux_x86_64/STAR --outFilterIntronMotifs RemoveNoncanonicalUnannotated --runThreadN 2 --outTmpDir /pathdir/ --outSAMtype BAM SortedByCoordinate --genomeDir /pathfordatabaseformus/ --readFilesIn XXX.clean.fq.gz --readFilesCommand zcat Thanks for all the guys who offer me help! |
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#2 | |
Senior Member
Location: NY Join Date: Feb 2009
Posts: 161
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you can check check Log.progress.out for the current mapping speed and progress. Are you trying to map all 9 samples at the same time with 2 threads for each job? If so, you need to use shared memory option, e.g. --genomeLoad LoadAndKeep. Without shared memory, the genomes for each sample have to be loaded in RAM, which requires ~9*25 GB. A simpler option would be to map one sample at a time with 12 threads. Cheers Alex |
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#3 | |
Member
Location: chicago Join Date: Nov 2012
Posts: 19
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#4 | |
Senior Member
Location: NY Join Date: Feb 2009
Posts: 161
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please post or email me the Log.out file from the failed single sample 12-thread run. Cheers Alex |
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#5 |
Member
Location: chicago Join Date: Nov 2012
Posts: 19
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Thanks for your help, but the project is in a hurry, so I have decided to change to tophat as the aligner, and have deleted all the related output file from STAR.
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Tags |
mouse, rna-seq, star aligner |
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