De novo genome assembly: what every biologist should know | Nature Methods
The effect of variant interference on de novo assembly for viral deep sequencing | bioRxiv
Genes | Free Full-Text | Reference Guided De Novo Genome Assembly of Transformation Pliable Solanum lycopersicum cv. Pusa Ruby
Applications | Biotech
Long walk to genomics: History and current approaches to genome sequencing and assembly - ScienceDirect
Tools and Strategies for Long-Read Sequencing and De Novo Assembly of Plant Genomes: Trends in Plant Science
Hypermutability of autism genes: lessons from genome sequencing | Beyond the Ion Channel
Theragen Bio | Global genome service provider and AI-based biopharmaceutical company
Introduction to de novo genome assembly for Illumina reads - Bioinformatics Documentation
An example workflow for high-throughput whole genome sequencing in bacteria.
De Novo Sequencing | Assemble novel genomes
Reference-guided de novo assembly approach improves genome reconstruction for related species | BMC Bioinformatics | Full Text
Whole genome sequencing - PacBio
Genetic variation and the de novo assembly of human genomes | Nature Reviews Genetics
Theragen Bio | Global genome service provider and AI-based biopharmaceutical company
Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation: Cell
Whole Genome de novo Assembly |Supporting de novo assembly training |Course |WGS sequencing | data analysis| Workshop
De novo genome assembly – NGS Analysis
Whole genome sequencing data and de novo draft assemblies for 66 teleost species | Scientific Data
Overview of whole genome sequencing approaches. a De novo assembly... | Download Scientific Diagram
De novo assembly of large eukaryotic genomes with long nanopore reads, and scaffolding using Pore-C
Enhanced De Novo Assembly of High Throughput Pyrosequencing Data Using Whole Genome Mapping | PLOS ONE
A field guide to whole‐genome sequencing, assembly and annotation - Ekblom - 2014 - Evolutionary Applications - Wiley Online Library
Analysis workflow to assess de novo genetic variants from human whole-exome sequencing - ScienceDirect
