Closed Arknights2 closed 3 months ago
Please capture the full error message. I need it for reference.
Sorry for not showing more information about this error
I added this part of the main information in the link
Log file:
2024-06-04 12:49:23, 475-data-ERROR-Command failed with exit code 255
2024-06-04 12:49:23, 476-data-ERROR -
alignment.report.tsv:
Didn't reach the end of sequence file, which might be corrupted!
Terminates in the process of generating the 01.data file
Chromap reported an error when aligning. Can you take a screenshot of the 01.data directory? I might suggest you rerun the command analysis.
Thank you for your reply
I have repeated the calculation three times with the same error
I didn't have this problem when I was dealing with other files, only this sample had a problem, which made me very confused
This is the first time I have seen this error. I want to see the information in the alignment.report.tsv file.
--fastq1 Sample1_1.fq.gz,Sample2_1.fq.gz \
--fastq2 Sample1_2.fq.gz,Sample2_2.fq.gz \
Is the datas one sample? sample1?sample2?
Thank you for your reply
I have just re-checked the files and the data are samples from the same person
For privacy purposes, I have hidden the path of some files
The alignment.report.tsv file is shown to you as a screenshot
Most of the content is repetitive, such as: "Loaded sequence batch successfully in 0.41s, number of sequences: 500000." and "Mapped 500000 read pairs in 3.99s."
https://github.com/haowenz/chromap/issues/134 refer to this, check the integrity of the input fastq files.
Thank you for your help, I will go to test as soon as possible!
Thank you very much for your help! I have found the problem and it was indeed due to incomplete fastq files.
Dear Professor
I encountered such an error when using dnbctools to process the offline data
scATAC data were analyzed, and the script followed the github prompts strictly
dnbc4tools atac run \
--fastq1 Sample1_1.fq.gz,Sample2_1.fq.gz \
--fastq2 Sample1_2.fq.gz,Sample2_2.fq.gz \
--genomeDir /human_hg38 \
--name DIPSEQT1 --threads 20
There are no problems in the other several samples for the time being. I sincerely ask how you can solve this error