Third Generation Sequencing. Today Illumina – Solexa sequencing technology 454 Life sciences – 454 sequencer Applied Biosystem – SOLiD system Tomorrow.

Slides:



Advertisements
Similar presentations
High throughput sequencing Barbera van Schaik
Advertisements

Schulich School of Medicine & Dentistry The University of Western Ontario London Regional Genomics Centre Next Generation Sequencing Meeting April 1, 2010.
MCB Lecture #15 Oct 23/14 De novo assemblies using PacBio.
Capillary Electrophoresis and the Human Genome
Next–generation DNA sequencing technologies – theory & practice
High-Throughput Sequencing Technologies
Current Sequencing Technologies and Data Generation
Bioinformatics Lectures at Rice
Next-generation sequencing
The past, present, and future of DNA sequencing Dan Russell.
Canadian Bioinformatics Workshops
Greg Phillips Veterinary Microbiology
Some new sequencing technologies. Molecular Inversion Probes.
CS273a Lecture 9, Aut08, Batzoglou CS273a Lecture 9, Fall 2008 Quality of assemblies—mouse N50 contig length Terminology: N50 contig length If we sort.
1 Next Generation Sequencing Itai Sharon November 11th, 2009 Introduction to Bioinformatics.
$399 Personal Genome Service $2,500 Health Compass service $985 deCODEme (November 2007) (April 2008) $350,000 Whole-genome sequencing (November 2007)
CS 6293 Advanced Topics: Current Bioinformatics
Computational Molecular Biology Biochem 218 – BioMedical Informatics Doug Brutlag Professor.
Next Generation DNA Sequencing Platforms: Evolving Tools for
GENOME SEQUENCING. I. Genome sequencing The Sanger Method (1977) Denaturation +priming Polymerization.
NGS Data Generation Dr Laura Emery. Overview The NGS data explosion Sequencing technologies An example of a sequencing workflow Bioinformatics challenges.
Update on Next-Generation Sequencing
High-Throughput Sequencing Technologies
Molecular Biology Dr. Chaim Wachtel April 4, 2013.
Sequencing Technologies and Applications at JGI
Finishing the Human Genome
Sequencing Technologies
High Throughput Sequencing Methods and Concepts
Introduction to next generation sequencing Rolf Sommer Kaas.
PERFORMANCE COMPARISON OF NEXT GENERATION SEQUENCING PLATFORMS Bekir Erguner 1,3, Duran Üstek 2, Mahmut Ş. Sağıroğlu 1 1Advanced Genomics and Bioinformatics.
Bioinformatics and Sequencing Relevant to SolCAP
High Throughput Sequencing Methods and Concepts Cedric Notredame adapted from S.M Brown.
Sequencing at the speed of life. Simple is beautiful.
A statistical base-caller for the Illumina Genome Analyzer Wally Gilks University of Leeds.
Genomics: READING genome sequences ASSEMBLY of the sequence ANNOTATION of the sequence carry out dideoxy sequencing connect seqs. to make whole chromosomes.
De Novo Genome Assembly - Introduction Henrik Lantz - BILS/SciLife/Uppsala University.
Stratton Nature 45: 719, 2009 Evolution of DNA sequencing technologies to present day DNA SEQUENCING & ASSEMBLY.
How will new sequencing technologies enable the HMP? Elaine Mardis, Ph.D. Associate Professor of Genetics Co-Director, Genome Sequencing Center Washington.
Molecular Biology Dr. Chaim Wachtel May 28, 2015.
SEQUENCING – THE BENCHTOPS. Roche 454 Junior Same technology as 454 FLX Read length: 400 bases Paired-end 100,000 reads 12 hours (instrument time) Output.
Welcome to UW-Madison, the WNPRC, and O’Connor Lab! MHC Genotyping Workshop November 7 th – 11 th, 2011 Madison, Wisconsin.
De Novo Genome Assembly - Introduction
Presented by Jonas Korlach, Ph.D. Chief Scientific Officer, Pacific Biosciences Wednesday, March 18, :-- AM – --:-- AM Location:HIR, UM SMRT Sequencing.
Sequencing technologies and Velvet assembly Lecturer : Du Shengyang September 29 , 2012.
DNA Replication “It has not escaped our notice that the specific pairing we have postulated immediately suggests a possible copying mechanism for the genetic.
DNA Sequencing Technology and its Applications in Evolution Research Julie Urban, Ph.D. Assistant Director, Genomics & Microbiology Laboratory NC Museum.
Genomics: READING genome sequences ASSEMBLY of the sequence ANNOTATION of the sequence carry out dideoxy sequencing connect seqs. to make whole chromosomes.
When the next-generation sequencing becomes the now- generation Lisa Zhang November 6th, 2012.
Introduction to Illumina Sequencing
BME 130 – Genomes Lecture 4 Sequencing technology II Next generation sequencing.
Next-generation sequencing technology
DNA Sequencing Second generation techniques
Next generation sequencing
Introduction to next generation sequencing
DNA Sequencing -sayed Mohammad Amin Nourion -A’Kia Buford
Next-generation sequencing technology
DNA is Data and DNA is a Machine
Sequencing technology and assembly
Biology is the science of reverse-engineering life
SOLEXA aka: Sequencing by Synthesis
B3- Olympic High School Bioinformatics
2nd (Next) Generation Sequencing
High-throughput sequencing techniques
The characterisation of mtDNA deletions using long-read sequencing
Technology Experimental Design Cost Estimation
High-Throughput Sequencing Technologies
High-Throughput Sequencing Technologies
Next-generation DNA sequencing
BF nd (Next) Generation Sequencing
Presentation transcript:

Third Generation Sequencing

Today Illumina – Solexa sequencing technology 454 Life sciences – 454 sequencer Applied Biosystem – SOLiD system Tomorrow Helico – Genetic Analysis Systems Pacific Bioscience – Singel Molecule Real Time System Oxford Nanopore – Nanopore sequencing Life technologies - Ion Torrent

Helico – Genetic Analysis Systems Helico – True Singel Molecule sequencer Pacific Bioscience – Singel Molecule Real Time System Oxford Nanopore – Nanopore sequencing Life technologies - Ion Torrent Helicos® Genetic Analysis System Performance Specifications SEQUENCING PERFORMANCE AS OF MARCH 1, 2010 Routine Usage Specifications 1 Strand Output 600M to 1B usable strands per run 12 to 20M usable strands per channel Sample Throughput Multiplexing capabilities up to 96 samples per channel with molecular barcoding. Up to 4,800 samples per run. Total Output 21 to 35 Gigabases per run 420 to 700 Megabases per channel Read Length 25 to 55 bases in length 35 average length Accuracy>99.995% consensus accuracy at >20X coverage Raw Error Rate Substitution 0.2% Insertion 1.5% Deletion 3.0% Template Size20 to 8,000 bases % GC Coverage<20% coverage variation for % GC (E. coli) Instrument Performance / Configuration Flow Cells 1 flow cell or 2 flow cells processed simultaneously 25 independent channels per flow cell Sequencer Throughput > 1 Gigabases per hour 2