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Population-scale genotyping using pangenome graphs

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Hi, I have regenotyped 9000+ samples and gotten a small set of 72 samples with all genotype (GT) results to unknown (./.) The other 9000 samples have around 2400 structural...

Hi: when i run graphtyper,it broken with the error,that means the computer node's cpu cant satisfy the graphtyper runnning? if so,when i run the script with 350 samples, what is...

Using a large library of breakpoints, a job was submitted on the GIAB HG002 sample for each chromosome using 8 threads. Most chromosomes completed in under 8 hours except chromosome...

Why is the filter a PASS for these 3 variants but the FT=FAIL1. Also what is the best software to compare these calls with the GIAB benchmark? The Ref All...

Hello, I'm trying to use Graphtyper as it seems to be fast and to scale well to many samples. Very easy to install and run so far.. but I'm unsure...

I've been running tests on various data sets, and have had a few cases where `graphtyper genotype_sv` makes VCFs with almost every site having zero depth and a genotypes of...

Graphtyper can create variants where the END position is lower than POS. This results in a warning from bcftools concat: ``` Concatenating ./chr10/010000001-011000000.vcf.gz[W::vcf_parse] INFO/END=9321046 is smaller than POS at chr10:9321047...

bug

Hi, I have 400 WGS samples and use manta+graphtyper2 to call SV. But I got an error. graphtyper genotyper_sv : No regions specified. Either use --region or --region_file option to...

Running graphtyper on GRCh38 with alt contigs, I get the following fatal error on chr6: ``` [constructor.cpp:159] FAI index has no entry for contig/chromosome 'HLA-DRB1*13' ``` Both the FASTA file...

bug

Hi Manta has three variants file:diploidSV.vcf.gz ,candidateSV.vcf.gz and candidateSmallIndels.vcf.gz so ,should i merge the corresponding which file type(candidateSV.vcf.gz ? discard diploidSV.vcf.gz andcandidateSmallIndels.vcf.gz) to the config.sh of make_graphtyper_pipeline.sh? In addition, the...