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Confusion in Tophat2 input files

dear all,

This might be very silly question but i hope you can help to clear my doubts

from TopHat mannual

tophat [options]* <genome_index_base> <reads1_1[,...,readsn_1]&gt; [reads1_2,...readsn_2]<="" p="">

Now, if i have a control and treated biological triplicate samples as paired-end reads what will be the right command

1) tophat [options]* <genome_index_base> control1_1 control1_2 tophat [options]* <genome_index_base> control2_1 control2_2 tophat [options]* <genome_index_base> control3_1 control3_2

tophat [options]* <genome_index_base> Treated1_1 Treated1_2
tophat [options]* <genome_index_base> Treated2_1 Treated2_2
tophat [options]* <genome_index_base> Treated3_1 Treated3_2

OR

2) tophat [options]* <genome_index_base> control1_1,control2_1,control3_1 control1_2,control2_2,control3_2 tophat [options]* <genome_index_base> Treated1_1,Treated2_1,Treated3_1 Treated1_2,Treated2_2,Treated3_2

OR

3) tophat [options]* <genome_index_base> control1_1,control2_1,control3_1,Treated1_1,Treated2_1,Treated3_1 control1_2,control2_2,control3_2,Treated1_2,Treated2_2,Treated3_2

OR

Something else

If I can use more than option than what is difference between them

Thanks in advance

rna-seq tophat alignment

I think you should run tophat for each sample separately to produce a bam file for each sample. I mean for example you should run tophat on control1-1 and control1-2 (paired-end) once then control 2-1, control 2-2, etc independently

1 answer

Alignment is performed per sample, i.e. the command is ran for each sample separately. So that would be option 1.

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