This repo will sumarize state of art variant calling methods
https://github.com/ding-lab/somaticwrapper
https://github.com/ding-lab/TinJasmine
https://github.com/ding-lab/GermlineWrapper.workflow
https://github.com/ding-lab/TinDaisy
HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) to a population of human genomes as well as to a single reference genome. https://www.nature.com/articles/s41587-019-0201-4#code-availability https://github.com/DaehwanKimLab/hisat2 http://daehwankimlab.github.io/hisat2/ https://anaconda.org/bioconda/hisat2
https://www.clinmedjournals.org/articles/jggr/journal-of-genetics-and-genome-research-jggr-7-048.pdf