Closed aman21392 closed 2 years ago
please check your genome file index, make shure you index with samtools index and picard CreateSequenceDictionary R=ref.fa O=ref.dict The code must use table to split, not "".
hey gaoyubang, I completed the run of nanom6A but I didn't find any document related to the final output result. which told about what is in the document and in the output file what the column denotes. So I didn't know which file and which column I looked to know the modification states. As you have given a model in your pipeline is it also good for taken those models or not. Thanks in advance for giving valuable information.
ratio.0.5.tsv file is empty in my case it means it does not detect any modification then. Can you please tell me why it is empty. This is the only file which empty. Thanks in advance
You can try to decrease the number of --support in predict_sites.py.
ok thanks
Hi I used the below command and it gives an error: (nanom6A_env) aclab@aclab:/Drive7/nanom6A$ python /home/aclab/nanom6A_2021_3_18/predict_sites.py --cpu 70 -i result -o result_final -r anno.bed -g /Drive1/new_human/Homo_sapiens.GRCh38.dna.primary_assembly.fasta --model /home/aclab/nanom6A_2021_3_18/bin/model/ --support 5
As you suggested In another issue to use print(faidx1,faidx2) in predict_sites.py 512 line; these will tell us, what is wrong:
File "/home/aclab/nanom6A_2021_3_18/predict_sites.py", line 513 sys.exit("please check your genome file, make shure it's end with fa or fasta!\n") ^ IndentationError: unexpected indent
As you saw above I used a reference fasta file and it downloaded from the ensemble. So please can you solve this issue. Thanks in advance