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Hi,
I am not sure about what is happening here. I use the program on my data (which are non human) and everything seems fine until this step. Then the vcf output file at the end is empty.
Step 3: Validation...
Converting SAM to BAM file, and then Sort and index the BAM file......
[bam_sort_core] merging from 0 files and 11 in-memory blocks...
[bwa_index] Pack FASTA... 0.00 sec
[bwa_index] Construct BWT for the packed sequence...
[E::bwa_idx_load_from_disk] fail to locate the index files
[E::bwa_idx_load_from_disk] fail to locate the index files
Hi, it should be because no TEs were detected in the earlier step. We currently make the tools to run with human genome. Maybe you could check the reference coordinates, is it named "chr1-24,X,Y"?
Hi,
I am not sure about what is happening here. I use the program on my data (which are non human) and everything seems fine until this step. Then the vcf output file at the end is empty.
Step 3: Validation...
Converting SAM to BAM file, and then Sort and index the BAM file......
[bam_sort_core] merging from 0 files and 11 in-memory blocks...
[bwa_index] Pack FASTA... 0.00 sec
[bwa_index] Construct BWT for the packed sequence...
[E::bwa_idx_load_from_disk] fail to locate the index files
[E::bwa_idx_load_from_disk] fail to locate the index files
Here is my command line to launch the program
perl /home/ubuntu/ERVcaller-1.4/ERVcaller_v1.4.pl -i Dmel_chr2L_sim_100X_150 -f .fq.gz -H /home/ubuntu/genome_Del_1.fasta -T /home/ubuntu/ref_TE.fasta -t 12 -S 20 -BWA_MEM -I /home/ubuntu/ -O /home/ubuntu/Dmel_100X_sim/ -r 150
Thank you in advance for you help!
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