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Segmentation during scanning for optimal CRF weight  #43

@kuangzhuoran

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@kuangzhuoran

Hello:

RFMIX v2.03-r0 - Local Ancestry and Admixture Inference
(c) 2016, 2017 Mark Koni Hamilton Wright
Bustamante Lab - Stanford University School of Medicine
Based on concepts developed in RFMIX v1 by Brian Keith Maples, et al.

This version is licensed for non-commercial academic research use only
For commercial licensing, please contact cdbadmin@stanford.edu

--- For use in scientific publications please cite original publication ---
Brian Maples, Simon Gravel, Eimear E. Kenny, and Carlos D. Bustamante (2013).
RFMix: A Discriminative Modeling Approach for Rapid and Robust Local-Ancestry
Inference. Am. J. Hum. Genet. 93, 278-288

Loading genetic map for chromosome Chr1 ... done
Mapping samples ... 29 samples combined
Scanning input VCFs for common SNPs on chromosome Chr1 ... 956161 SNPs
Loading haplotypes... done
Defining and initializing conditional random field...
setting up CRF points and random forest windows...
computing random forest window spacing overlay...
initializing apriori reference subpop across CRF...
setting up random forest probability estimation arrays... done
Defining and initializing conditional random field... done
9589734 (17.3%) variant alleles 0 (0.0%) missing alleles

Generating internal simulation samples...
Internally simulated 154 samples from 1 randomly selected reference parents.

Scanning for optimal CRF Weight....
/slurmState/slurmSpool/slurmd/job775448/slurm_script: line 17: 10145 Segmentation fault (core dumped) ./rfmix -f sp1.chr1.vcf -r sp2.chr1.vcf -m sp2.pop -g sp1.genetic.map -o outer --chromosome=Chr1

my command is : ./rfmix -f sp1.chr1.vcf -r sp2.chr1.vcf -m sp2.pop -g sp1.genetic.map -o outer --chromosome=Chr1
What could this be about? = =

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