Closed morggen13 closed 1 year ago
Dear @morggen13,
Try adding ENV="TOLERATE_NUMERICAL_ERRORS=1"
to the command line, like
hyphy gard --alignment env_seq.fasta --rv Gamma ENV="TOLERATE_NUMERICAL_ERRORS=1;"
Errors like this indicate some soft of numerical instability, and generally can be ignored unless a fatal irrecoverable error is generated.
Best, Sergei
Thank you! I'm running this now. Is there something I could be doing to speed up the analysis? I'm working with 382 HIV-1 envelope sequences. I saw in previous versions you could limit the max number of breakpoints but it looks like that's not supported any more.
Dear @morggen13,
Couple of things.
N
= number of cores).mpirun -np N HYPHYMPI gard...
--mode Faster
flag.--max-breakpoints K
); make sure you are using the latest version of HyPhy.GARD has a sweet spot of ~20-50 sequences both in terms of speed and breakpoint resolution. The more sequences you give it, the larger the recombination event has to be for it to detect it (more nts per partition, for example).
A simple approach to do this is outlined in https://github.com/veg/hyphy/issues/1448
Best, Sergei
Stale issue message
While running this gard command
hyphy gard --alignment env_seq.fasta --rv Gamma
I got the following error: Internal error in _LikelihoodFunction::GradientLocateTheBump: in the Brent loop iteration 1. -21012391.17418955 / -21012321.85947149. I saw in a previous issue that this is likely because the sequences are too divergent. This was something I was worried about because my sequences were sampled over several decades (1990s to 2020s). Is there a way for me to figure out if this is what is causing this error? Or something I could do to remedy the issue?