Whole Genome Sequencing
Identify mutations and disease states
Whole Genome Sequencing determines the complete DNA sequence of an organism’s genome
Single nucleotide polymorphisms (SNP’s)
Short indels (insertions / deletions)
Copy number variations (CNV’s)
Structural variations
Duplications
Translocations
Inversions
Pseudogenes
Haplotypes
Repeat sequences
Generate novel complete reference genomes
Perform comparative genomics – individuals, families, populations
Examine time-course variations of complete genomes
Perform genome-wide association studies (GWAS)
WGS can be applied to many research fields
Drug development
Cancer research
Infectious diseases
Population genetics
Variant studies
Affordable sequencing for genomes under 50 Mb
Bacteria
Bacteriophage
Viruses
Plasmids
Yeast
Parasites
Fungi
Small prokaryotic, eukaryotic & archaeal genomes
We offer several sequencing options to deliver comprehensive results
Short-Read Only | Long-Read Only | Hybrid Assembly (short-read + long-read) | |
---|---|---|---|
Single nucleotide polymorphism (SNP) | Yes | Yes | Yes |
Short indels (insertions / deletions) | Yes | Yes | Yes |
Copy number variations (CNV’s) | Yes | Yes | Yes |
Q-score (Phred score) > Q30 (99.9% basecall or consensus accuracy) | Yes | Yes | Yes |
Large structural variants | No | Yes | Yes |
Long repeat sequences | No | Yes | Yes |
Translocations | No | Yes | Yes |
Inversions | No | Yes | Yes |
Duplications | No | Yes | Yes |
Long N50 length | No | Yes | Yes |
Generate a reference genome | No | No | Yes |
“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.”