Oxford Nanopore Technologies

Slides:



Advertisements
Similar presentations
Genome Biology for Programmers Lecture Series: Illumina Sequencing
Advertisements

High throughput sequencing Barbera van Schaik
Nanopore Membranes for Single-Molecule Detection and Characterization Anna Schibel, Ryuji Kawano and Henry S. White University of Utah October 26, 2007.
MOL8002 – Molecular mechanisms of host defence Methods of molecular biology Recognition of nucleic acids hybridization, sequencing, PCR, arrays Protein.
High-Throughput Sequencing Technologies
Next-generation sequencing
1 Genetics The Study of Biological Information. 2 Chapter Outline DNA molecules encode the biological information fundamental to all life forms DNA molecules.
1 Learning to Detect Objects in Images via a Sparse, Part-Based Representation S. Agarwal, A. Awan and D. Roth IEEE Transactions on Pattern Analysis and.
Family Resemblances Why do siblings often look alike?
Introduction to DNA.
GTL User Facilities Facility II: Whole Proteome Analysis Michelle V. Buchanan.
AP Biology: Chapter 14 DNA Technologies
explain how crime scene evidence is
1 Chapter 7 Chapter 7 DNA Fingerprinting Learning Goals: o Explain how crime scene evidence is collected and processed to obtain DNA o Describe how radioactive.
Regulatory factors 1) Gene copy number 2) Transcriptional control 2-1) Promoters 2-2) Terminators, attenuators and anti-terminators 2-3) Induction and.
Journal Meeting Jung-Yun Ko DNA Sequencing & ABI DNA Sequencer.
The Future of NVIS Display Measurement ALI Advanced Seminar, 2006Optronic Laboratories Dr. Richard Young Optronic Laboratories, Inc.
Single Molecule Mass Spectrometry Using a Single Nanopore Dr. John J. Kasianowicz Colleagues: NIST: J. Robertson, V. Stanford Brazil: O. Krasilnikov, C.
How will new sequencing technologies enable the HMP? Elaine Mardis, Ph.D. Associate Professor of Genetics Co-Director, Genome Sequencing Center Washington.
Intel Confidential – Internal Only Co-clustering of biological networks and gene expression data Hanisch et al. This paper appears in: bioinformatics 2002.
NANO Week District 205. What is Nanotechnology?  Understanding and using objects that are less than 100 nm in size  Nanotechnology can be used in (let’s.
The Polymerase Chain Reaction (DNA Amplification)
Objectives: Introduce the students to digest genomic DNA by restriction endonucleases. Observe the results of digestion on agarose gel electrophoresis.
Chromosomes Genes Where do you find DNA? All mature cells contain DNA except the red blood cells DNA is found in the nucleus Small amounts of DNA are.
Third Generation Sequencing. Today Illumina – Solexa sequencing technology 454 Life sciences – 454 sequencer Applied Biosystem – SOLiD system Tomorrow.
Forensic Science DNA Analysis 1. History of Biological Evidence in Forensics  DNA fingerprinting  Also known as DNA profiling  Used with a high degree.
Active Lecture Questions Copyright © 2011 Pearson Education Inc. Chapter 3 Biological Molecules.
Library QA & QC Day 1, Video 3
Chapter 13: DNA Quantitation.  Determining the amount of DNA is a sample is essential  A narrow concentration range is required for PCR  Must use human-specific.
Introduction to Illumina Sequencing
Explain how crime scene evidence is
Explain how crime scene evidence is
Cancer Genomics Core Lab
Single Molecule Mass Spectrometry Using a Single Nanopore
Nanopore Sequencing Technology and Tools:
Delivering a Pharmacogenomics NGS service in 5 working days
Prokaryotic and Eukaryotic Cells: What do all cells have in common?
Elena Maftei Technical University of Denmark DTU Informatics
扩增产物的毛细管电泳分离 ( Amplification of capillary electrophoresis separation )
Figure 1. Workflow of the LISH assay. Step 1
SOLEXA aka: Sequencing by Synthesis
B3- Olympic High School Bioinformatics
Nanopore Sequencing Technology and Tools:
Nanopore Sequencing Technology and Tools for Genome Assembly:
ELECTRON SPIN RESONANCE Dylan Prendergast Advanced Lab, Fall 2007
History of Biological Evidence in Forensics
Explain how crime scene evidence is
How to Build a Horse: Final Report
The characterisation of mtDNA deletions using long-read sequencing
Explain how crime scene evidence is
High-Throughput Sequencing Technologies
Genetics: From Genes to Genomes
High-Throughput Sequencing Technologies
The Study of Biological Information
Volume 96, Issue 2, Pages (January 2009)
Validation and Implementation of a Custom Next-Generation Sequencing Clinical Assay for Hematologic Malignancies  Michael J. Kluk, R. Coleman Lindsley,
Received 24th March 2010, Accepted 14th July 2010
Research Support Network (RAI)
History of DNA Fingerprinting
BF nd (Next) Generation Sequencing
Jméno: Jiří Kudr Datum :
Explain how crime scene evidence is
explain how crime scene evidence is
Explain how crime scene evidence is
Genomic DNA Sample Preparation
Chapter 3 Biological Molecules.
Chapter 3 Biological Molecules.
Genomic & RNA Profiling Core Facility
Next Generation Sequencing Market. Report Description and Highlights According to Renub Research market research report “Next Generation Sequencing (NGS)
Presentation transcript:

Oxford Nanopore Technologies Nanopore Sequencing

Introduction to nanopore sensing A nanopore: a nano-scale hole. Biological: a pore-forming protein (e.g. α-Hemolysin) in a membrane (e.g. lipid bilayer) Solid-state: in synthetic materials ( e.g. silicon nitride or graphene) Hybrid: formed by a pore-forming protein set in synthetic material

Nanopore sensing Ionic current passed through membrane by setting a voltage across the membrane. Disruption in current detected when analyte passes through the pore or near its aperture. Characteristic disruption indentifies the molecule in question.

Nanopore DNA sequencing DNA polymer or individual nucleotides pass through the nanopore. Detected by a adaptor molecule ( e.g. Cyclodextrin). Tunnelling electrodes based detectors. Capacitive detectors Graphene based nano-gap or edge state detectors.

Nanopore DNA sequencing Strand sequencing: Sequencing in real-time as the intact DNA polymer passes through the nanopore. Exonuclease sequencing: Individual nucleotides pass through the nanopore by the aid of processive exonuclease.

Strand Sequencing Snapshot from movie at http://www.nanoporetech.com

Electron-based read out Four different magnitudes of disruption which can be classified as C, G, A or T Modified base, e.g. methylated cytosine, can be directly distinguished from the four standard bases

Strand Sequencing Hairpin structure: Sense and anti-sense sequencing Advantages in Data Analysis Snapshot from movie at http://www.nanoporetech.com

Exonuclease Sequencing Snapshot from movie at http://www.nanoporetech.com

Exonuclease Sequencing Adapter molecule (cyclodextrin): Accuracy averaging 99.8% Identification of meC Snapshot from movie at http://www.nanoporetech.com

Working strategy MinION: a miniaturised sensing instrument Portable. Field-deployable. Requires minimal sample prep. Compatible with blood serum, plasma and whole blood.

Working strategy GridION system Uses single-use, self-contained cartridge. Can be used as a single instrument: Node Can be used in a cluster, connected through network. Low power and space required. Permits scheduling and multiplexing.

Workflow versatility No fixed run time Run until... sufficient data Can be run one or more nodes for minutes or days. Data analysis takes place in real time. Longer run enables collecting more data points. Run until... sufficient data The GridION system enables users to run an experiment until sufficient data has been collected to reach a predetermined experimental endpoint.

Run until... sufficient data

Oxford nanoporeDNA sequencing: applications Besides Personalised Medicine Diagnosis and treatment Pharmacogenomics Prevention Security/defence

Advantages over present sequencing technologies Real-time sequencing strategy. No strand amplification needed. No bias due to sequencing amplification. Low cost: trying to fulfil the target of $1000 per human genome. Lager read size: read size is limited only by preparation. No requirement for large amounts of high-performance disk storage. Large-scale structural variation can be detected at lower depth of coverage. Enable long-range haplotyping. No need for expensive and time-consuming mate pair library construction.

Thank you