Dear community, does anyone know of a nanopore variant caller which can perform multisample (not single sample) SNV calling on long reads (similar to eg …
Does anyone know if BWA Mem -M flag (mark shorter split hits as secondary) will have a detrimental effect on structural variation calling using split …
Hi, Does anyone ever used MMR or others ambiguous reads resolution tools on bam files before to do variant calling? Does it improvement results accuracy? …
I'm looking at a DELLY annotated file, I am having some difficulty visualizing the difference between PairEndReadSupport, SplitReadSupport, TumorVariantCount, TumorSplitVariantCount, TumorReadCount. Can someone familiar with …
<p>Recently, I am calling translocations from the whole genome sequencing data by using DELLY. But it reports many results, so How to validate a translocation …