Comments (1)
Related Issues (20)
- Can't find reference fasta file
- increase sensitivity
- Guidelines/tips for filtering VCFs after running strelka2 germline?
- Got WARNING and ERROR info when using StrelkaSomaticWorkflow HOT 2
- INFO/DP field not reported
- make process bug
- Does input fastq need process of splicing in advance?
- CONFIGURATION ERROR: Reference genome mismatch:
- Which command to use for somatic calling and RNA sequencing?
- Long error using the code below
- How to detect somatic mutations with allele frequencies nearly 0.01? HOT 1
- Only the first Genome Segment called when putting entire chromosome in .bed file
- inconsistent reproducibility of variants
- Number of AD, ADF and ADR should be "R"
- Failing to index VCF file
- Incorrect handling of non-N nucleotides with quality zero after Q-score binning
- All variants being labeled as "LowEVS" HOT 1
- Meaning of taskExitCode -9 HOT 1
- Scripts to extract variant allele frequency (VAF) HOT 1
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