Nanopore sequencing at NGI and Clinical Genomics

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Nanopore sequencing at NGI and Clinical Genomics

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Please select your primary area of interest.

Animal Genetics & Ag Research

Biomanufacturing QC

Cancer Research

Cell & Gene Therapy

Clinical Disease Testing & Screening

Clinical Oncology

Conservation, Biodiversity, Environment

Disease Mechanism – Common & Complex

Food Testing (safety, auth, prod)

Human ID & Forensics

Infectious disease

Microbial genomics

Pathogen surveillance

Plant Genetics & Ag Research

Plasmid, Cloning, AAV

Population Studies (National / MOH / T2T)

Rare and Undiagnosed Disorders (RUGD)

Please select your primary technique.

Barcoding & Sample ID

Bioinformatics

Cell Free (DNA RNA cf ct circ ec)

Chromatin Conformation

DeNovo Assembly

Direct RNA

Exome Sequencing

Fragmentomics

Gene Editing

HLA Typing

Low-Pass Sequencing & CNV

Metagenomics & Species ID

Methylation / Epigenomics

PGTA or NIPT

Pharmacogenomics

Protein Seq Apps

Single Cell & Spatial

SNVs & Phasing

Structural Variation

Targeted Sequencing

Transcriptomics

Whole-Genome Sequencing

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<100 GB

>100 GB

30 to 100 GB

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