Nextflow Modules
Showing module(s) with keyword "nanopore"
| Module | Keywords | Description |
|---|---|---|
| nf-core/artic/aligntrim | artic primer trimming amplicon genomics sequencing nanopore illumina | Standalone version of fieldbioinformatics aligntrim. Soft clips amplicon scheme primer sites in BAM/SAM files. |
| nf-core/canu | Assembly pacbio hifi nanopore | Accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads. |
| nf-core/chopper | filter trimming fastq nanopore qc | Filter and trim long read data. |
| nf-core/dragonflye | bacterial assembly nanopore | Assemble bacterial isolate genomes from Nanopore reads |
| nf-core/emu/abundance | metagenomics 16S nanopore | A taxonomic profiler for metagenomic 16S data optimized for error prone long reads. |
| nf-core/filtlong | nanopore quality control QC filtering long reads short reads | Filtlong filters long reads based on quality measures or short read data. |
| nf-core/gstama/collapse | tama_collapse.py isoseq nanopore long-read transcriptome gene model TAMA | Collapse redundant transcript models in Iso-Seq data. |
| nf-core/gstama/merge | gstama gstama/merge long-read isoseq nanopore tama trancriptome annotation | Merge multiple transcriptomes while maintaining source information. |
| nf-core/hypo | assembly polishing nanopore illumina | Assembly polisher using short (and long) reads |
| nf-core/medaka | assembly polishing nanopore | A tool to create consensus sequences and variant calls from nanopore sequencing data |
| nf-core/melon | profile metagenomics melon classification long reads nanopore | Performs taxonomic profiling of long metagenomic reads against the melon database |
| nf-core/miniasm | assembly pacbio nanopore | A very fast OLC-based de novo assembler for noisy long reads |
| nf-core/myloasm | assembly metagenome long-read pacbio nanopore | Myloasm is a de novo metagenome assembler for long-read sequencing data. It takes sequencing reads and outputs polished contigs in a single command. |
| nf-core/nanocomp | bam fasta fastq qc nanopore | Compare multiple runs of long read sequencing data and alignments |
| nf-core/nanofilt | nanopore filtering QC | Filtering and trimming of Oxford Nanopore Sequencing data |
| nf-core/nanomonsv/parse | structural variants nanopore cancer genome somatic structural variations mobile element insertions long reads | Parse all the supporting reads of putative somatic SVs using nanomonsv. After successful completion, you will find supporting reads stratified by deletions, insertions, and rearrangements. A precursor to "nanomonsv get" |
| nf-core/nanoplot | quality control qc fastq sequencing summary nanopore | Run NanoPlot on nanopore-sequenced reads |
| nf-core/porechop/abi | porechop_abi adapter nanopore | Extension of Porechop whose purpose is to process adapter sequences in ONT reads. |
| nf-core/porechop/porechop | adapter nanopore demultiplexing | Adapter removal and demultiplexing of Oxford Nanopore reads |
| nf-core/pychopper |