Comments (6)
Instructions from the author for no replicate sample run is detailed here:
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Instructions from the author for no replicate sample run is detailed here:
Thank you for your reply. But it seems that you may misunderstand it. The manual only tells what to do when missing replicate samples but not only one condition(without control). I just want to get one sample's psi for each splicing event. Could "--Condition2_fileNum_threshold" be set to 0 when we only want to get one sample's result?
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I see. It seems then that you just want the PSI values for each condition as well, which is what I also want to calculate and have asked the author (issue above yours). Running only one sample may not be currently possible, but if you could calculate PSI values for each condition (not delta PSI), it would suit your purpose.
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I see. It seems then that you just want the PSI values for each condition as well, which is what I also want to calculate and have asked the author (issue above yours). Running only one sample may not be currently possible, but if you could calculate PSI values for each condition (not delta PSI), it would suit your purpose.
Thank you. It seems that we can only wait for author's reply.
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Hi, Sorry for the late reply. If you just want to get the gene corresponding splicing event and psi value with one sample, one way to do it is to copy your single bam file, and re-named it as it it were a different file (copy as many as you want, for both condition 1 and condition 2 reps), and feed them to JUM, run through the original pipeline, but set pvalue to 1 in the last step. In that case you will have a full atlas of splicing events profiled from the sample bam file.
from jum.
Hi, Sorry for the late reply. If you just want to get the gene corresponding splicing event and psi value with one sample, one way to do it is to copy your single bam file, and re-named it as it it were a different file (copy as many as you want, for both condition 1 and condition 2 reps), and feed them to JUM, run through the original pipeline, but set pvalue to 1 in the last step. In that case you will have a full atlas of splicing events profiled from the sample bam file.
Thank you so much. I'll try it.
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Related Issues (20)
- The length of the RNA-seq reads is inconsistent
- PSI values per condition HOT 1
- error occurred when running JUM_B.sh HOT 1
- Recommendations for sequencing depth HOT 1
- JUM output Splicing events Visualization tools HOT 1
- Correcting for batch effects while running JUM HOT 1
- JUM (v2.0.2 and up) stops and get killed at a certain step HOT 6
- Error of Rscript at write.table step HOT 1
- filtering outputs from cutoff p-value=1 HOT 3
- perl errors while running JUM_B HOT 1
- Perl Error due to a sample not having AS on one contig HOT 2
- JUM a lot of error... but finish runnnig an output empty file. HOT 1
- _trash_out file should be empty! HOT 2
- Regarding delta-PSI value, control-treatment vs treatment-control HOT 1
- Regarding Error "NONE" after running JUM_C.sh HOT 1
- JUM_A: ERROR: ... not sorted lexicographically HOT 1
- Error when running JUM_A.sh
- JUM_2-3.sh missing in JUM_3.0.0
- Error when running JUM step A HOT 21
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