A survey of tools for variant analysis of next-generation genome sequencing data http://bib.oxfordjournals.org/content/15/2/256.short #NGS #Tools #Survey #Variant
#Mapping #sequencing #reads to a #reference #genome with #Bowtie2: a step-by-step guide https://insidedna.me/tutorials/view/how-to-use-bowtie2-read-mapping
#Contiguous and #accurate de novo #assembly of #metazoan genomes with modest long read coverage https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/gkw654