Fundamentals of Genome Assembly - YouTube
BecA Bioinformatics
Rapid hybrid de novo assembly of a microbial genome using only short reads: Corynebacterium pseudotuberculosis I19 as a case study - ScienceDirect
De novo genome assembly – NGS Analysis
De novo genome assembly versus mapping to a reference genome
De novo assembly of prokaryotic and large eukaryotic genomes
De novo genome assembly
De Novo Sequencing | Assemble novel genomes
Assembler for de novo assembly of large genomes | PNAS
Filling in the gaps: GapPredict can complement repertoire of tools used to resolve missing DNA sequences in genome assemblies | Genome Sciences Centre
Hybrid genome assembly - Wikipedia
The effect of variant interference on de novo assembly for viral deep sequencing | BMC Genomics | Full Text
De novo genome assembly: what every biologist should know | Nature Methods
De novo genome assembly – NGS Analysis
Slide Deck: Slide Deck: Hands-on: Unicycler assembly of SARS-CoV-2 genome with preprocessing to remove human genome reads / Assembly
Sequence Mapping, Part 2: De Novo Assembly | by ShortLong-Seq Bioinformatics | Medium
Whole Genome de novo Assembly |Supporting de novo assembly training |Course |WGS sequencing | data analysis| Workshop
What is de novo assembly? - The Sequencing Center
Introduction to de novo genome assembly for Illumina reads - Bioinformatics Documentation
Comparison of reference assembly and de novo assembly. A) Reference... | Download Scientific Diagram
De novo assembly of large eukaryotic genomes with long nanopore reads, and scaffolding using Pore-C
De Novo Sequencing | Assemble novel genomes
Sequencing from scratch: reference genomes and de novo sequence assembly – HudsonAlpha Institute for Biotechnology
Reference-guided de novo assembly pipeline. Raw reads get quality... | Download Scientific Diagram
De Novo Genome Assembly
Plants | Free Full-Text | Reference-Guided De Novo Genome Assembly to Dissect a QTL Region for Submergence Tolerance Derived from Ciherang-Sub1
High-throughput pipeline for the de novo viral genome assembly and identification of minority variants from Next-Generation Sequencing of residual diagnostic samples | bioRxiv
