Nextflow pipeline to assemble genomes from long reads.
-
Updated
Nov 6, 2024 - Nextflow
Nextflow pipeline to assemble genomes from long reads.
Meiotic Recombination Detection Pipeline with PacBio HiFi sequencing reads
Adapter+Barcode trimming from Pacbio HiFi reads
trimmomatic for long reads
A Nextflow pipeline for variant calling and annotation using PacBio Hi-Fi sequencing reads.
Variant calling pipeline for Pacbio Hifi reads
pacbiohifi read analyzer using recursion
profiling pacbiokmers and filtering pacbio kmers
multipattern trimmomatic for long reads
streaming visualization of pacbiohifi reads
pacbio/oxford nanopore long reads repeat coverage estimation
Scripts for de-novo genome assembly, assembly polishing, QC and post-assemble analyses of HiFi whole genome sequence data and downstream pangenomics analyses to identify structural variants
a streamlit application for graphical analyisis of pacbiohifi reads
codegetter for illumina, pacbio and oxford long read and short reads
polyATGC pacbio/oxford nanopore estimator
Add a description, image, and links to the pacbio-hifi-sequencing-reads topic page so that developers can more easily learn about it.
To associate your repository with the pacbio-hifi-sequencing-reads topic, visit your repo's landing page and select "manage topics."