Closed Imogen-D closed 2 years ago
Hi,
You cannot restart the analysis from where it crashed. But you can split your analysis into chromosomes and merge it afterward. You can find a detailed tutorial for this at https://github.com/isinaltinkaya/angsd-troubleshooting-guide/blob/main/doGLF_chr-by-chr.MD
For outputting a beagle file please see http://www.popgen.dk/angsd/index.php/Glf_files.
Hope this helps, please feel free to reopen the issue if you have more questions about this.
Best, Isin
Hey - fun challenge! I would restart from scratch but on individual chromosomes (-r chr1 for example), run all those in parallel with -doGlf 2 to export straight to beagle. Then you can concatenate the beagle files (but tbh one chromosome is probably good enough for relatedness)
On Mon, Sep 19, 2022 at 6:07 PM Imogen Dumville @.***> wrote:
Hi,
I had a run of >500 RADseq samples that crashed due to running out of CPU hours (oops). However, my mafs and glf.pos files have finished writing to different chromosome numbers. I need a glf.gz file for downstream ngsrelate. Is there any way of A) restarting a run from the current end point or B) seeing which chromosome the glf.gz file (which is binary) is finished/written up to, so I can rerun (and then concatenate) the chromosomes that have not finished?
Also, is there any way of converting from the glf binary beagle to a 'normal' beagle file?
Many thanks!
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-- cheers Misha matzlab.weebly.com
Hi,
I had a run of >500 RADseq samples that crashed due to running out of CPU hours (oops). However, my mafs and glf.pos files have finished writing to different chromosome numbers. I need a glf.gz file for downstream ngsrelate. Is there any way of A) restarting a run from the current end point or B) seeing which chromosome the glf.gz file (which is binary) is finished/written up to, so I can rerun (and then concatenate) the chromosomes that have not finished?
Also, is there any way of converting from the glf binary beagle to a 'normal' beagle file?
Many thanks!