SVNN: an efficient PacBio-specific pipeline for structural variations calling using neural networks | BMC Bioinformatics | Full Text
Quickstart - how to polish a genome assembly — Nanopolish 0.8.4 documentation
Minimap2: versatile pairwise alignment for nucleotide sequences | Semantic Scholar
The NCBI Eukaryotic Genome Annotation Pipeline
QIAGEN Bioinformatics Manuals
Featherweight long read alignment using partitioned reference indexes | Scientific Reports
Frontiers | Benchmarking Low-Frequency Variant Calling With Long-Read Data on Mitochondrial DNA
How does using a multi part index affect the accuracy? · Issue #141 · lh3/ minimap2 · GitHub
Accurate spliced alignment of long RNA sequencing reads | bioRxiv
Genes | Free Full-Text | Exploring Semi-Quantitative Metagenomic Studies Using Oxford Nanopore Sequencing: A Computational and Experimental Protocol
Long-Read Isoform Definition with FLAIR
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing | Nature Biotechnology
Introduction to the principles and methods underlying the recovery of metagenome‐assembled genomes from metagenomic data - Goussarov - 2022 - MicrobiologyOpen - Wiley Online Library
Features | Geneious Prime
Data structures used for hash table: Minimizers extracted from the... | Download Scientific Diagram
What is the most accurate short (ish) read aligner?
Minimap2: versatile pairwise alignment for nucleotide sequences | Semantic Scholar
Abundance estimation after Minimap2 alignment · Issue #207 · gpertea/stringtie · GitHub
Accelerating Minimap2 for accurate long-read alignment on GPUs
cotton genome variations database
Microorganisms | Free Full-Text | Nanopore Sequencing Is a Credible Alternative to Recover Complete Genomes of Geminiviruses
cotton genome variations database
Minimap2 workflow depicting its three key modules: (i) seeding, (ii)... | Download Scientific Diagram
Minimap2 transcriptome mapping – Jan's Blog of Bioinformatics Bits
FLAMES
Minimap2 | Geneious
