Whole Genome Sequencing
Identify mutations and disease states
Complete genomic structure
Whole genome sequencing determines the complete DNA sequence of an organism’s genome
Identify genomic variants
Single nucleotide polymorphisms (SNP’s)
Short indels (insertions / deletions)
Copy number variations (CNV’s)
Structural variations
Duplications
Translocations
Inversions
Pseudogenes
Haplotypes
Repeat sequences
Benefits
Generate novel complete reference genomes
Perform comparative genomics – individuals, families, populations
Examine time-course variations of complete genomes
Perform genome-wide association studies (GWAS)
Whole genome sequencing applications
WGS can be applied to a variety of research fields
Drug development
Cancer research
Infectious diseases
Population genetics
Variant studies
From plasmids to people
We can sequence genomes for any organism
Microbes
Bacteria
Bacteriophage
Viruses
Plasmids
Small Genomes
Yeast
Parasites
Fungi
Small prokaryotic, eukaryotic & archaeal genomes
Large Genomes
Humans
Plant and Animal
Large eukaryotic genomes
Actionable reports
WGS reports include rich, detailed data
Sequence alignment metrics
Gene variant and mutation lists
Polymorphism types
Amino acid changes
Codon changes
Protein effects
Metadata
Metagenomic species ID (optional)
All projects include FASTQ data files
Leading research institutions trust us
“This was the fastest turnaround time ever! From cells to full genome sequence in 5 days! We will definitely work together in the future. Thank you!”
“The results look excellent. It’s been a pleasure working with you.”