Open jonassibbesen opened 4 years ago
I got same problem exactly.
@parkchanhee I've been waiting for Developers. please help us.
@jonassibbesen did you solve this problem? I can't wait any more.
@a00101 No, not yet.
@jonassibbesen @a00101 I also see this issue. I remember it works for me previously. But I don't know why it happens now.
Hi,
I am trying to build an index with variation from the 1000 genomes project. I first tried to build an index using all variation, but I got the following error:
exceeded integer bounds, remove adjacent SNPs, use haplotypes, or switch to a large index (--large-index)
.I am already using haplotypes so I decided to filter low frequent alleles. I tried removing all alleles with a frequency below 0.01 and 0.05 resulting in ~14M and ~8.5M variants, respectively. However, I still got the same error. Would it help if I increased
--inter-gap
and--intra-gap
inhisat2_extract_snps_haplotypes_VCF.py
? I was thinking that longer haplotypes might help to not make the number of nodes explode.Next I decided to try to switch to a large index as suggested using
--large-index
on the filtered variants. However, that resulted in a crash with the following error:Command terminated by signal 6
I am only adding variants and not splice-junctions. Hope you are able to help me solve this.
Thanks,
Jonas