Hi,
I downloaded the pre-compiled binary for sambamba (sambamba_v0.6.6_linux.tar.bz2) from https:...
Can anybody send me the tutorial for Exome-Seq? I am interested to learn the variant calling.
Hi,
I am working on variant calling on fungal genomes. I have Illumina HiSeq reads. I am new to ...
Sambamba is a high performance modern robust and fast tool (and library), written in the D pro...
I'm working on somatic variant calling from mouse exome sequencing data, and my pipeline is based...
I would like to filter VCF files with a maximum depth filter, so removing variants with a coverag...
Hi everyone,
I am new to bioinformatics field. So please apologize for my questions that I am not...
Dear all,
I have launched sambamba with this command:
sambamba markdup -r -t 8 --overflow-l...
After reading the Board Institute tutorial on [variant calling with ALT contigs][1], just wonder ...