Long-read Human Whole Genome Resequencing
Long-read Whole Genome Sequencing Services are performed with PacBio and Oxford Nanopore platforms, long read sequencing approaches provide the opportunity to more accurately and reliably detect SNP、InDel、SV and CNV at a much higher resolution.
Features and Advantages
Better performance in genome region with repetitive sequences where SVs tend to occur
Better read coverages in GC-poor or GC-rich regions
NO genome sequencing bias introduced by PCR amplification during library construction
Higher sensitivity and accuracy of variation detection
Sequencing Standards
Guaranteed ≥100 Gb/Cell Nanopore pass data with Q>7
Guaranteed ≥90 Gb/Cell PacBio Revio HiFi data
- Standard sequencing coverage 15X/45G data
Sampling Requirements
Genomic DNA PacBio HiFi CCS : m≥15 μg，c≥80 ng/μL
Genomic DNA Normal Nanopore library : m≥9 μg，c≥90 ng/μL
- Genomic DNA Nanopore Ultra long library : m≥16 μg，c≥153 ng/μL
Service Details
Typical 30 working days from sample QC acceptance to data delivery
Superior bioinformatics anlysis team support
Expedited services are available, contact your local representative for details
- Reports and output data files are delivered in industry standard file formats: BAM, .xls, .png and FASTQ data
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