Comments (8)
Here are my scripts:
sprint main -p 10 -1 $FQ1 -2 $FQ2 $REF $SPRINT_OUTPUT_FOLDER $BWA $SAMTOOLS
python getA2I.py 0 $SPRINT_OUTPUT_FOLDER $A_TO_I_PATH
"SPRINT_identified_all.res", "SPRINT_identified_hyper.res", and "SPRINT_identified_regular.res" should be in the "$SPRINT_OUTPUT_FOLDER"
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- '//' and ‘/’ have the same function in linux;
- You can directly download the executable program of SPRINT, BWA (0.7.12) and SAMTOOLS (1.2) from "https://github.com/jumphone/SPRINT/tree/master/bin/" and "https://github.com/jumphone/SPRINT/tree/master/samtools_and_bwa" . After clicking the file, there is a button for "download raw file". And please remember to make them executable “e.g. chmod 777 sprint”
- python | getA2I.py | 0 | path_to_directory_of_sprint_output | path_to_A_to_I_result
from sprint.
Hi there, I reran SPRINT using the correct versions of bwa and samtools and I definitely noticed more output files created so it fixed something but I'm not getting any .res
files outputted.
Here is my out file:
$1: INT, 1 for strand-specific sequencing data.
$2: OUTPUT_DIR of SPRINT
$3: OUTPUT_PATH of A-to-G RESs
Traceback (most recent call last):
File "/home/user/github/SPRINT/utilities/getA2I.py", line 15, in <module>
fi=open(regular)
IOError: [Errno 2] No such file or directory: 'path/SPRINT/Output/NO-01/tmp/SPRINT_identified_regular.res'
I have all sorts of output files in my designated output file from SPRINT main and I have run multiple different samples and none of them have outputted any sort of .res
file. I thought maybe that was supposed to be an output from getA2I.py
but I'm now seeing that that is part of what SPRINT main outputs. I looked into sprint main to try and figure out why the .res
noticed in sprint_main.py around line 625 that there is good amount of lines commented out that involved the .res
files so I thought maybe it had something to do with that. I could really use a bit more description as to what I could possibly be doing wrong or why I am not getting the expected output.
Here is what is contained in each of the output folders that I have "successfully" run with no error (copied from my SPRINT output directory).
all_combined.zz hyper_mskAG.snv transcript_mskAG_all.zz.dedup.genome.zz
all_combined.zz.sorted hyper_mskTC.snv transcript_mskAG_all.zz.dedup.snv
baseq.cutoff PARAMETER.txt transcript_mskAG_all.zz.dedup.snv.genome.snv
genome regular.snv transcript_mskAG_all.zz.dedup.snv.genome.snv.sort
genome_all.zz.dedup transcript transcript_mskTC
genome_all.zz.dedup.snv transcript_all.zz.dedup transcript_mskTC_all.zz.dedup
genome_mskAG transcript_all.zz.dedup.genome.zz transcript_mskTC_all.zz.dedup.genome.zz
genome_mskAG_all.zz.dedup transcript_all.zz.dedup.snv transcript_mskTC_all.zz.dedup.snv
genome_mskAG_all.zz.dedup.snv transcript_all.zz.dedup.snv.genome.snv transcript_mskTC_all.zz.dedup.snv.genome.snv
genome_mskTC transcript_all.zz.dedup.snv.genome.snv.sort transcript_mskTC_all.zz.dedup.snv.genome.snv.sort
genome_mskTC_all.zz.dedup transcript_mskAG
genome_mskTC_all.zz.dedup.snv transcript_mskAG_all.zz.dedup
from sprint.
Your input path of getA2I.py is the "tmp" folder. Please directly use the output folder "path/SPRINT/Output/NO-01/".
from sprint.
Appreciate the quick response - I reran my script with your suggested path modification and came up with the same error.
Traceback (most recent call last):
File "/path/github/SPRINT/utilities/getA2I.py", line 15, in <module>
fi=open(regular)
IOError: [Errno 2] No such file or directory: '/path/SPRINT/Output/NO-01/SPRINT_identified_regular.res'
A .res
file is supposed to be included in the output from sprint_main, correct? I was not seeing in the tmp directory but I am not seeing it in the parent directory either (the specified output dir).
from sprint.
I got it working - thanks for your help :)
from sprint.
Related Issues (20)
- # HOT 19
- How to set the parameter -ss for non-strand-specific RNA-seq? Thank you. HOT 2
- Is the trimming first 6 bases step included in your pipeline? HOT 2
- Why the rate of A-to-G deteced by SPRINT is very low ? HOT 3
- Generated binary files not working HOT 6
- zz2sam.py hard-codes strandedness HOT 5
- how to calculate the no. of editing sites present in 3' UTRs and CDS and 5'TRS??? HOT 3
- Effect of editing sites on the condon changes HOT 3
- SPRINT installation Error HOT 7
- Differential RNA Editing HOT 3
- Error during run HOT 6
- Execution problem HOT 3
- No output after execution HOT 4
- import error HOT 3
- reverse strandedness -ss 1 or -ss 2 HOT 4
- No results in final result files HOT 2
- calculation time HOT 1
- What ref .fa file to use for sprint main after prepare? HOT 1
- Some editing sites can not be identified but it has editing reads when viewing with IGV. HOT 3
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