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Population-scale genotyping using pangenome graphs

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Thank you for your brilliant work on Graphtyper2. I have encountered one issue during the use of Graphtyper2. For example: SV=chr1:54719:UG, END=54720, End-Start=1, but SV size =50 SV=chr1:3212695:DG, END=3212826, End-Start=131,...

Apologies if I missed this information. I noticed that the same variant can have multiple entries in the output VCF. The ALT field seems to suggest it's because they represent...

Dear Hannes Thank you so much for developing such a nice program. I used GraphTyper on Manta and CNVnator outputs (after getting the union of SVs by svimmer) successfully. However,...

Hi @hannespetur The genotyping accuracy of structural variants has a large impact on the subsequent analysis. Currently, I usually use `graphtyper (the latest version)` and `paragraph` to realize this progress....

Dear @hannespetur I found many variants are with "PASS" for `FT` but not `FILTER`, as the following example. Should I filter out these?Thanks for your attention. ``` 1 273082885 1:273082885:FG...

Hi! I am using `graphtyper genotype` with the `--vcf` flag to genotype a specific set of input variants. However, it seems that Graphtyper does not only genotype these variants, but...

Hi, i have a query wrt to the tool and its utility in genotyping cancer samples ? what model does it assume in genotyping, is it diploid model ? Can...

Hello, thank you for making this awesome tool! I have a question about the "OLD_VARIANT_ID" field. I regenotyped a VCF of SV sites called with Manta. In the Graphtyper output,...

I'd like to include the Long-read assemblies file when identifying structural variations.How do I get Long-read assemblies SVS_VCF files?

I've started a run of graphtyper with a command for each chromosome of my reference: graphtyper genotype --threads 16 --verbose --sams=bamlist --region=H1_8_48-4_1 REF.fna graphtyper genotype --threads 16 --verbose --sams=bamlist --region=H1_8_48-4_2...