gsukrit

Results 8 issues of gsukrit

Hi, I would like to know if the command _nanopolish eventalign_ changes the file size/content of the sequencing_summary file we specify in the command. If so, why? Since we are...

Hi, I was trying out the nanopolish index which consistently gave me the error as follows: [readdb] indexing /DATA/BioLab/Sukriti/PF_FAS70460_IIT/ACD_pass_FAST5/barcode02/ error getting group name size I had barcoded 3 samples in...

Hi, I tried to run this tool for some DRS Nanopore reads. However, the last command (m6anet inference) didn't execute and throws the following error: ![image](https://github.com/GoekeLab/m6anet/assets/81628564/442e1b67-ff88-4e40-9c41-4d022ff78e45) If you can, please...

Hi team, I would like to have clarity on the column header _transcript_position_ in the output file of _data.site_proba.csv__ generated after the command _m6anet inference_. Does it indicate the position...

If we wish to get the read level information of the methylated transcript, can we use the second column i.e. read levele and k-mer probability of the middle A of...

Hi team, I would like to have clarity on the column header position in the output file of site_level_prediction (CHEUI solo outputs). Does it indicate the position of modified base...

Hi team, I was trying to run the command: python3 ../scripts/CHEUI_predict_model2.py -i read_level_m6A_predictions_sorted.txt -m ../CHEUI_trained_models/CHEUI_m6A_model2.h5 -o site_level_m6A_predictions.txt The command got executed, and the site-level file was made, but it also...

Hi Team, I basecalled my data using Dorado in Super accuracy mode for 5mC and 5hmC in CG and 6mA all context and aligned with the reference genome during basecalling....

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