Human whole genome sequencing (WGS) provides a genome-wide view of genetic variation across coding and non-coding regions. Short- and long-read options can support detection of SNPs, indels, copy number variants and structural variants for inherited disease, cancer, population genomics and complex disease research.

Whole exome sequencing (WES) focuses sequencing on protein-coding regions, where many functionally important variants are found. It offers a targeted approach for variant discovery in rare and inherited disease research, cancer genomics, complex disease studies and population genetics, with downstream variant detection and annotation.

Plant and animal whole genome sequencing profiles genome-wide variation across model and non-model species. WGS can support detection of SNPs, indels, copy number and structural variants for population genomics, breeding, GWAS, comparative genomics, trait research, adaptation and genome evolution studies.

De novo genome sequencing supports species where a suitable reference genome is limited or unavailable. Short-read, long-read and chromosome-level assembly strategies can help build new reference genomes, resolve complex or repetitive regions, and support genome annotation, comparative genomics, evolution and trait-related research.

Microbial whole genome sequencing supports bacteria, fungi, viruses and other microorganisms. Microbial WGS can support strain comparison, genetic variation analysis, comparative genomics and functional annotation across microbiology, epidemiology, agriculture and environmental research.

Microbial de novo sequencing builds genome assemblies without relying on an existing reference, making it useful for novel or less-characterised microorganisms. Short- or long-read sequencing can support draft or higher-contiguity assemblies, genome annotation, functional exploration, comparative genomics and evolutionary or ecological studies.

Shotgun metagenomics analyses total DNA from complex microbial communities without targeted amplification. It supports taxonomic profiling, functional gene and pathway analysis, metagenome assembly, antimicrobial resistance analysis and genome-resolved approaches, with short- and long-read sequencing options available depending on study goals and sample requirements.

Amplicon sequencing uses targeted marker regions such as 16S rRNA, 18S rRNA and ITS to profile microbial community composition, diversity and relative abundance. Short-read and full-length amplicon sequencing options can support high-throughput microbiome studies or higher taxonomic resolution for selected research designs.

PlasmidGo uses Oxford Nanopore long-read sequencing for primer-free whole plasmid sequencing and full-construct verification. The workflow can help confirm insert sequence and orientation, backbone integrity, repetitive or complex regions and unexpected structural changes, with streamlined online ordering for customer-provided plasmid DNA.

Human whole genome sequencing (WGS) provides a genome-wide view of genetic variation across coding and non-coding regions. Short- and long-read options can support detection of SNPs, indels, copy number variants and structural variants for inherited disease, cancer, population genomics and complex disease research.

Whole exome sequencing (WES) focuses sequencing on protein-coding regions, where many functionally important variants are found. It offers a targeted approach for variant discovery in rare and inherited disease research, cancer genomics, complex disease studies and population genetics, with downstream variant detection and annotation.

Plant and animal whole genome sequencing profiles genome-wide variation across model and non-model species. WGS can support detection of SNPs, indels, copy number and structural variants for population genomics, breeding, GWAS, comparative genomics, trait research, adaptation and genome evolution studies.

De novo genome sequencing supports species where a suitable reference genome is limited or unavailable. Short-read, long-read and chromosome-level assembly strategies can help build new reference genomes, resolve complex or repetitive regions, and support genome annotation, comparative genomics, evolution and trait-related research.

Microbial whole genome sequencing supports bacteria, fungi, viruses and other microorganisms. Microbial WGS can support strain comparison, genetic variation analysis, comparative genomics and functional annotation across microbiology, epidemiology, agriculture and environmental research.

Microbial de novo sequencing builds genome assemblies without relying on an existing reference, making it useful for novel or less-characterised microorganisms. Short- or long-read sequencing can support draft or higher-contiguity assemblies, genome annotation, functional exploration, comparative genomics and evolutionary or ecological studies.

Shotgun metagenomics analyses total DNA from complex microbial communities without targeted amplification. It supports taxonomic profiling, functional gene and pathway analysis, metagenome assembly, antimicrobial resistance analysis and genome-resolved approaches, with short- and long-read sequencing options available depending on study goals and sample requirements.

Amplicon sequencing uses targeted marker regions such as 16S rRNA, 18S rRNA and ITS to profile microbial community composition, diversity and relative abundance. Short-read and full-length amplicon sequencing options can support high-throughput microbiome studies or higher taxonomic resolution for selected research designs.

PlasmidGo uses Oxford Nanopore long-read sequencing for primer-free whole plasmid sequencing and full-construct verification. The workflow can help confirm insert sequence and orientation, backbone integrity, repetitive or complex regions and unexpected structural changes, with streamlined online ordering for customer-provided plasmid DNA.