Closed Xiaofei-git closed 2 years ago
Hi @hyunhwan-jeong, I think it should work with mixture of SR and PE FASTQs. I tried to remove CTRL_1_R2.fastq in example folder and run SalmonTE.py count, and it went through. So, I believe it should work out.
But, I still can't get MAPPING_INFO.csv and condition.csv. Do you know the reason for this?
Thanks a lot!
Best,
Xiaofei
Hi @hyunhwan-jeong, I think it should work with mixture of SR and PE FASTQs. I tried to remove CTRL_1_R2.fastq in example folder and run SalmonTE.py count, and it went through. So, I believe it should work out.
But, I still can't get MAPPING_INFO.csv and condition.csv. Do you know the reason for this?
Thanks a lot!
Best,
Xiaofei
@hyunhwan-jeong Could you help me to confirm if it can take the folder of mix SR and PE?
I think I made a mistake for the test of mix SR and PE. The run did not go through and I got as below:
SalmonTE.py quant --reference=hs --outpath=quant_out_test_mix --exprtype=count example_2
2021-09-23 05:08:34,748 Starting quantification mode
2021-09-23 05:08:34,748 Collecting FASTQ files...
2021-09-23 05:08:34,781 A paired-end sample and a single-end sample are placed together.
Dear @hyunhwan-jeong ,
After running
, I am expecting get
But, I missed MAPPING_INFO.csv and got phenotype.csv instead of condition.csv?
Another question, could SalmonTE take mix PE and SR data in input folder (e.g. there are both single end and paired end fastq in example folder, is that OK for SalmonTE to get right outputs)?
Thanks a lot!
Best,
Xiaofei