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Showing module(s) with keyword "longread"

Module Keywords Description
nf-core/kled genomics longread structural variants An ultra-fast and sensitive structural variant detection tool for long-read sequencing data.
nf-core/shasta nanopore de-novo assembly longread The goal of the Shasta long read assembler is to rapidly produce accurate assembled sequence using DNA reads generated by Oxford Nanopore flow cells as input. Please note Assembler is design to focus on speed, so assembly may be considered somewhat non-deterministic as final assembly may vary across executions. See https://github.com/chanzuckerberg/shasta/issues/296.