Long-read genome sequencing (ONT or PacBio Technology)
Long-read RNaseq (ONT or PacBio Technology)
Direct RNA sequencing (ONT Technology)
Amplicon sequencing (PacBio Technology)
Long-read Bioinformatics Tier 1 (Mapping of sequencing reads to reference genome. Data available in .bam/.sam/.parquet formats)
Long-read Bioinformatics Tier 2 (Error correction, variant calling, and phasing analysis of SNPs, small and large INDELs, and other SVs. Data available in .vcf/.parquet/.csv formats)
Customized long-read sample workflow (such as "small non-coding RNA sequencing from frozen brain tissue" or "Long-read targeted sequencing of a customized gene panel")
Customized long-read bioinformatics pipelines (adapted to specific application with production grade, deployed to AWS cloud)
Specialty services
Clinical Pharmacogenomics (PGx) genotyping and Copy Number Variation (CNV) assay
PGx Enhancer (built on PacBio Technology)
de novo assembly long-read sequencing (built on Ultra-long nanopore sequencing + PacBio sequencing + bioinformatics Tier 3)
Long-read biomarker discovery solution (built on Nanopore sequencing + PacBio sequencing + bioinformatics Tier 3 - Access via Sequegenics Platform)
Exome Enhancer (built on PacBio Technology)
Let’s talk about long-read!
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