Comments (8)
Hi @Jarvis559,
Could you attach the full log file for debugging?
from pseudou-bidseq.
2024-01-10T125527.473221.snakemake.log
from pseudou-bidseq.
Seem that the log file is incomplete, which does not show the command that was used. What is the reference sequence you used in the data.yaml file.
from pseudou-bidseq.
Thanks for your reply! This is my first test data.yaml file:
reference:
contamination:
fa: /disk/user_18/jky_project/genome/Mesomycoplasma_hyorhinis_ATCC_17981/Mesomycoplasma_hyorhinis_ATCC_17981.fna
genes:
fa: /disk/user_18/jky_project/genome/GRCh38.p14/GRCh38.p14.sncRNA.fa
genome:
fa: /disk/user_18/jky_project/genome/GRCh38.p14/GCF_000001405.40_GRCh38.p14_genomic.fna
star: /disk/user_18/jky_project/index/star/GRCh38.p14/GRCh38.p14
samples:
HeLaWT-rep1-input:
data:
- R1: /disk/user_18/jky_project/BID_project/learning/rawdata/HeLa_input_1.fastq.gz
group: HeLaWT
treated: false
HeLaWT-rep1-treated:
data:
- R1: /disk/user_18/jky_project/BID_project/learning/rawdata/HeLa_BID_1.fastq.gz
group: HeLaWT
treated: true
HeLaWT-rep2-treated:
data:
- R1: /disk/user_18/jky_project/BID_project/learning/rawdata/HeLa_BID_2.fastq.gz
group: HeLaWT
treated: true
And now i am trying the second test without the input of contamination reference genome sequence:
# Max number of cores for all the running jobs at the same time
cores: 50
barcode: "NNNNNXXX-XXXNNNNNATCACG"
# NOTE: relative path of reference and sample data should relative to current config file, rather than workdir
reference:
genes:
fa: /disk/user_18/jky_project/genome/GRCh38.p14/GRCh38.p14.sncRNA.fa
genome:
fa: /disk/user_18/jky_project/genome/GRCh38.p14/GCF_000001405.40_GRCh38.p14_genomic.fna
star: /disk/user_18/jky_project/index/star/GRCh38.p14/GRCh38.p14
samples:
HeLaWT-rep1-input:
data:
- R1: /disk/user_18/jky_project/BID_project/learning/rawdata/HeLa_input_1.fastq.gz
group: HeLaWT
treated: false
HeLaWT-rep1-treated:
data:
- R1: /disk/user_18/jky_project/BID_project/learning/rawdata/HeLa_BID_1.fastq.gz
group: HeLaWT
treated: true
HeLaWT-rep2-treated:
data:
- R1: /disk/user_18/jky_project/BID_project/learning/rawdata/HeLa_BID_2.fastq.gz
group: HeLaWT
treated: true
from pseudou-bidseq.
This likely that the data you used did not contain reads that mapped to the "Mesomycoplasma_hyorhinis_ATCC_17981" reference which lead to zero size of bam file.
from pseudou-bidseq.
I will see if removing the step of alignment to the Mesomycoplasma_hyorhinis_ATCC_17981 genome works. Thank you very much!
from pseudou-bidseq.
Hi y9c!
Removing the step of alignment to the Mesomycoplasma_hyorhinis_ATCC_17981 genome works!
But I encountered two instances of automatic program termination. My command is nohup apptainer run docker://y9ch/bidseq &
in the terminal. And I always keep the terminal on. The attatchment is the two log files.
2024-01-11T111942.665433.snakemake.log
2024-01-12T003946.169422.snakemake.log
from pseudou-bidseq.
Great! If there are more questions, please let me know.
from pseudou-bidseq.
Related Issues (11)
- Detailed parameters of STAR HOT 5
- Low mapping ratio and lost reads after realigngap and filter HOT 3
- samFilter: /lib64/libc.so.6: version `GLIBC_2.28' not found HOT 15
- Filtering question HOT 1
- rcFastq HOT 15
- header of result HOT 1
- automatic program termination HOT 6
- barcode setting HOT 1
- Duplicated reads level is high HOT 1
- --bind error HOT 1
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