Comments (10)
Prof. Chen, I successfully ran the software by modifying the reference genome. For other species, chromosome number modification is a must. ERVcaller works great!!!
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nice, let me know if you have further questions.
Xun
from ervcaller.
Hi, I think you forgot to put the number of CPUs for "-t", like "-t 10". Also "-I" is for the folder containing the FASTQ files and "-O" for your output folder.
Thanks,
Xun
from ervcaller.
Prof. Chen, thank you very much for your reply. However I still have the same problem when running the code. Then how can I solve it?
from ervcaller.
Hi,
Have you run the test data yet? Btw, have you installed SEI-MEI successfully? if not, you could follow the steps in README. could you also show a list of files under the output folder?
Thanks,
Xun
from ervcaller.
yeah,SEI-MEI should be installed successfully.like this:
I tried the test data, but the same error was reported. Then ran my own data.
the output/ file is as follows:
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from ervcaller.
Hi,
I would suggest you run it with the test data first and then apply it to your datasets.
Few suggestions and tips for testing the tools:
-
please export the paths of all included tools, including SEI-MEI (see README file).
-
all references should be indexed with bwa, including the human reference genome and TE reference genome (see README file too).
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ERVcaller would support human chromosome IDs, such as "chr1", "chr2" and so on. If you are working on other species, you could try rename them.
Best,
Xun
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Okay, thanks again for your reply. I will try it again. Best wishes to you!!
from ervcaller.
yeah!Thank you!
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Related Issues (20)
- failed at step 3 HOT 3
- Problem in Step 2 HOT 5
- Error unexpected end of file HOT 1
- RNAseq data HOT 3
- [E::bwa_idx_load_from_disk] fail to locate the index files HOT 10
- Cannot remove "sort.bam.tmp.0000.bam" files HOT 2
- bwa-mem2 HOT 2
- Lack of "GQ" value in output.vcf and some question about "Merging" step HOT 10
- Some chromosomes don't harbour any variation HOT 5
- A question about the "INFOR" field HOT 4
- About using TGS data HOT 2
- Some chromosomes don't harbour any variation HOT 2
- Length of TSD HOT 2
- Assembly of the target ERV HOT 1
- Question of setting the -H parameter HOT 1
- A question of filter criteria in guide paper HOT 1
- Error in finding the input data under the provided sampleID HOT 2
- Cannot progress beyond step 2 HOT 5
- Assemble inserted virus sequence through intermediate output files HOT 8
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