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A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data

Results 21 adVNTR issues
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When --haploid option is given, the output format should be changed accordingly.

enhancement

Hi Mehrdad, I'm trying to run advntr on some PacBio reads mapped to hg38 and I'm using the hg38 models (hg38_selected_VNTRs_Illumina.db) however I get a `sqlite3.OperationalError` when running with the...

Hi there, adVNTR will not work unless the h5py version is changed to 2.10.0. Perhaps the conda environment could be updated to reflect this?

Hi, After installing the package, I'm having difficulty getting the genotype command to run on some pacbio bam files. Running the following; advntr genotype -p -a NA07019_SC034768.bam --update -m vntr_data/hg19_VNTRs.db...

Hi, apparently I have a multiprocess error when running adVNTR ; the command : advntr genotype --alignment_file $bam --working_directory $advntrDir/$bam_name --vntr_id 25561 --pacbio --frameshift -m ../hg19_selected_VNTRs_Pacbio.db -t $Ncpu the error...

Hi, when I download vntr_data_recommended_loci.zip , there are two files ( illumina and pacbio ). If I have Nanopore data, can I choose the pacbio file or do you have...

For VNTRs on chrY, we can first check if we can call homozygous calls for VNTRs on chrY and output the haplotype only if the call is confident.

hi, i installed the latest version of adVNTR (v1.32) using miniconda: conda install -c bioconda advntr, and erverything is well but i cannot add (create) a new .db ohh! i...

- `hg19_chromosomes/CombinedHG19_Reference.fa` is hard-coded in many places (ex. `src/reference_vntr.py`) - `chr9.fasta` is hard-coded in a supplementary script - chromosome names are defined in `settings.py`, and not using a sequence dictionary...