Haplotype-aware assembly of complex regions and small genomes

Scrambling paper analysis in R

Draft workflow for pairwise genome comparison. We recommend you use the new nf-core version instead: https://nf-cor.e/pairgenomealign

Repository to host tool-specific module files for the Nextflow DSL2 community!

Luslab nextflow modules

Color a sequence alignment (nucleotide or protein) to visualize haplotype/recombination blocks

Code (data preparation and analysis) for diffBase

OIST long read assembler