Single cell Nanopore sequencing data for Genotype and Phenotype
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Updated
Sep 5, 2024 - Python
Single cell Nanopore sequencing data for Genotype and Phenotype
HIV-64148, an integration of multiple long-read genome assemblers with a pipeline for analysis of HIV-1 genomic data from Oxford Nanopore Sequencing Technology or PacBio Real-Time (SMRT) Sequencing technology.
RawHash is the first mechanism that can accurately and efficiently map raw nanopore signals to large reference genomes (e.g., a human reference genome) in real-time without using powerful computational resources (e.g., GPUs). Described by Firtina et al. (published at https://academic.oup.com/bioinformatics/article/39/Supplement_1/i297/7210440)
Haplotype aware variant calling from long read sequence
NanoASV official repo
Dorado-basecalled reads improve old bacterial genome assembly
Pipeline to assemble oxford nanopore long sequencing reads and perform variant calling with long and short reads
Species-level Taxonomic Abundance from 16S rRNA Sequencing (STARS)
A bioinformatic pipeline for aligning amplicon reads to a DNA database based on Nextflow
Analysis of sequencing error profile for long read data.
Nextflow pipeline for analysis of direct RNA Nanopore reads
A generic best practice workflow for processing human Oxford Nanopore Technologies (ONT) sequencing data.
Nanopore sequencing experimental protocols and computational pipelines
zeo++ fork of the LSMO
Comprehensive pipeline for detection of TB from ONT adaptive sequencing and amplicon data.
A pipeline for high-quality bacterial genome construction using ONT sequencing
Rapid comprehensive adaptive nanopore-sequencing of CNS tumours set-up and analysis pipeline
This is just small command line pipeline to simplify going from ONT Unbasecalled data using Guppy to Assembly using Flye, all of the tools are existing tools.
Impact of lossy compression of nanopore raw signal data on basecall and consensus accuracy
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