Error message:
$ vechat <inut01>.fq -t 48 --platform ont -o <input01>.vechatCorrected.fq
Performing the 1 iteration for error correction...
Killed
perform variation graph based (haplotype-aware) error correction
[racon::Polisher::initialize] loaded target sequences 0.293457 s
[racon::Polisher::initialize] loaded sequences 0.275359 s
[racon::Polisher::initialize] error: empty overlap set!
Performing the 2 iteration for error correction...
perform linear sequence based error correction
[racon::Polisher::initialize] error: empty target sequences set!
Context:
I tried to error-correct a set of ONT reads using vechat v1.1.1 installed via bioconda and ended up with the error message above. I tried using vechat with two different sets of ONT input data, let's call them input01 and input19 here. In both cases I ended up with the error message above.
| input |
protocol |
mean read coverage |
file size |
| input01 |
amplicon seq |
10059 |
95 MB |
| input19 |
WGS |
4365 |
276 MB |
Hence, data is present and plenty.
Question:
Why do I end up with the error message given the vechat command above? Should I adjust some parameters?
Additional:
I don't expect the files to be corrupted. Tools like canu and mosdepth work fine on the same files. Also, I already retried using vechat with different thread numbers (-t 1, 16, 48).
Related issues:
Error message:
Context:
I tried to error-correct a set of ONT reads using
vechat v1.1.1installed via bioconda and ended up with the error message above. I tried using vechat with two different sets of ONT input data, let's call them input01 and input19 here. In both cases I ended up with the error message above.Hence, data is present and plenty.
Question:
Why do I end up with the error message given the vechat command above? Should I adjust some parameters?
Additional:
I don't expect the files to be corrupted. Tools like canu and mosdepth work fine on the same files. Also, I already retried using vechat with different thread numbers (
-t1, 16, 48).Related issues: