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ICRA step sam2pmp error #33

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@xiangyupan

Hi,
After successfully creating the database based several MAG files, another error happened when I run the step 2 ICRA by python.
My code is
from SGVFinder2 import single_file, get_sample_map from pandas import to_pickle read1 = '/storage/public/home/2024110144/00.Project/Diet/Tan_rumenMeta/01.rmHost/clean_data/Unknown_BW368-003R0001_1_kneaddata_paired_1.fastq' read2 = '/storage/public/home/2024110144/00.Project/Diet/Tan_rumenMeta/01.rmHost/clean_data/Unknown_BW368-003R0001_1_kneaddata_paired_2.fastq' DATABASE = '/storage/public/home/2024110144/00.Project/Diet/Sheep_MAG/rename/Sheep_db' jspi_file, jsdel_file = single_file( ... fq1=read1, ... fq2=read2, ... outfol='/storage/public/home/2024110144/00.Project/Diet/Sheep_MAG/rename/output',dbpath=DATABASE)

The bam file have generated normally. And I generated the stat file of the bam file:

Image

My error is as follows. As the error may be caused by the unpaired reads according to the error, then I have checked that the reads in bam are all paired and the fastq files are also paired. I am not sure what's wrong in my files. Hope for your reply. Thanks for your time and work.

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