Save 20% on PacBio Human Whole Genome Sequencing
Confidently identify causative pathogenic variants and novel disease-associated genes with the power of HiFi long-read sequencing. With an accuracy of 99.9% per base, uncover complete, accurate, and phased assemblies of the human genome, including regions previously inaccessible to other technologies.
Take advantage of our incredible offer and save 20%.
Unbiased coverage
Tandem repeats
Structural variant calling (fully phased)
Small variant calling with fully phased haplotypes
Segmental duplications
CNV analysis
CpG Methylation (5-methylcytosine)
Access regions of high homology (pseudogenes, dark regions)
Full analysis included - cohort analysis and variant filtering
TERMS and CONDITIONS
Orders must use Promo Code: PCBhWGS032024
Valid from 28 March, 2024 to 17 May, 2024. Quote acceptance and purchase order must be received prior to 23:59 AEST, 17 May, 2024.
Samples must be received by COB Friday, 31 May, 2024.
Discounts apply to AGRF list price only.
Deliverables
Minimum 60Gbp output
Minimum 10Kb read length
Complete variant calling analysis
All QC and library preparation is included with delivery of FASTQ files.
Additional charges apply for nucleic acid extraction or custom bioinformatics.
This promotion is not retrospective and cannot be used in conjunction with other orders, discounted pricing or current promotions.
Terms and conditions are subject to change without notice.