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can't finish the process #57
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Hello Maxim, I would recommend using fewer threads (try 3-5 at first), along with fewer loci. In our landscape analysis of TCGA data we used 2,530 loci (https://ascopubs.org/doi/suppl/10.1200/PO.17.00073), so 100,000 loci is overkill for MSI calling. |
Hi I used 65 threads for 10 loci. And i have problem. |
Try substantially reducing your thread count; even if you have sufficient CPU cores this many threads will probably be I/O limited. |
Hi @rbonneville , |
Hi,
I used 1 core and I solved my problem. It seems to be very strange.
Regards, Maxim
ср, 4 нояб. 2020 г. в 19:20, ghosholivia <[email protected]>:
… Hi @rbonneville <https://github.com/rbonneville> ,
I'm having the same issue. I had tried with thread 5 but it's been 4 hrs
and it is still running.
Can you guide me please?
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Yeah. It ran successfully but did it take 1 day for WGS bam |
This seems like a potential threading issue. If you notice stalling with many threads, could you please terminate the process and post a traceback? |
Yes, it ran successfully with low threads. Thanks. |
Hi,
I have some problems with MANTIS. I can't finish the process. I used WGS data (70 Gb - normal and 150 Gb - tumor) and 3 mln rows of loci bed basing on hg38 genome.
Also I used only chr16 from bam files (~2-3 Gb) and loci.bed for chr16 (100K) lines, but my process can't finish.
Though?
Microsatellite Analysis for Normal-Tumor InStability (v1.0.4)
/usr/bin/python3 /home/ubuntu/1/MANTIS/kmer_repeat_counter.py
-b /home/ubuntu/1/MANTIS/loci.bed2
-n /home/ubuntu/1/MANTIS/DNASeq_blood.sorted.chr16.bam
-t /home/ubuntu/1/MANTIS/DNASeq_cancer.sorted.chr16.bam
-o /home/ubuntu/1/MANTIS/1.kmer_counts.txt
--min-read-quality 25.0
--min-locus-quality 30.0
--min-read-length 35
--genome /home/ubuntu/1/MANTIS/hg38.fa
--threads 64
Getting repeat counts for repeat units (k-mers) ...
Regards, Maxim
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