Navigation:  Home > CGR > All Seminars

Tuesday 13 July
10:00-10:45	Caccamo, M (BBSRC)
	Sequencing Technologies – cheaper, faster and better	Meeting Room 2, CMS
10:45-11:30	Lunter, G (Wellcome trust Centre for Human Genetics)
	From calling bases to calling variants: experiences from the analysis of Illumina sequencing data	Meeting Room 2, CMS
11:40-12:25	Taylor, J (CSIRO)
	Looking under the hood; profiling genome function with sequencing	Meeting Room 2, CMS
13:30-14:10	Donnelly, P (University of Oxford)
	Whole-genome sequencing for medical and population genetics	Sem 1
14:10-14:50	Caccamo, M (BBSRC)
	Challenges behind crop resequencing	Sem 1
14:50-15:30	Clark, A (University of Cornell)
	Modeling allele-specific expression from RNA-seq data	Sem 1
16:00-16:30	Green, P (University of Washington, Seattle)
	Next-generation data analysis	Sem 1
16:30-17:00	Irizarry, R (Johns Hopkins University)
	What the 1000 genomes project tells us about systematic bias and batch effects in sec-gen data	Sem 1
17:00-17:30	Song, Y (UC Berkeley)
	Model-based base-calling and de novo error correction algorithms for short-read sequencing	Sem 1

Wednesday 14 July
09:00-09:30	Albers, C A (Cambridge)
	Calling small indels in the 1000 Genomes low-coverage and high-coverage pilots	Sem 1
09:30-10:00	Durbin, R (Wellcome Trust Sanger Institute)
	Efficient construction of overlap assemblies using suffix array based methods	Sem 1
10:00-10:30	Iqbal, Z (University of Oxford)
	Reference-free analysis of genetic variation	Sem 1
11:00-11:30	Marchini, J (University of Oxford)
	Genotype imputation with thousands of genomes	Sem 1
11:30-12:00	Abecasis, G (University of Michigan)
	Sequencing 1000s of Human Genomes	Sem 1
12:00-12:30	Kong, A (DeCode genetics)
	Phasing SNPs and sequences	Sem 1
16:00-16:30	Campbell, P (Wellcome Trust Sanger Institute)
	Analysis of whole cancer genomes	Sem 1
16:30-17:00	Shah, SP (BCCRC)
	Statistical models for inference of SNVs in cancer genomes	Sem 1
17:00-17:30	Down, T (University of Cambridge)
	Deconvolving the epigenome: analysis strategies for genome-wide studies	Sem 1

Thursday 15 July
09:00-09:30	Pickrell, J (University of Chicago)
	Understanding variation in mRNA processing with RNA sequencing	Sem 1
09:30-10:00	Jiang, H (Stanford University)
	Estimating Isoform-Specific Gene Expression Using Paired-End RNA-Seq	Sem 1
10:00-10:30	Marioni, J (University of Chicago)
	De novo assembly and evolutionary analyses of liver-expressed genes in 16 mammal species	Sem 1
11:00-11:30	Faulkner, G (University of Edinburgh)
	Transposed element RNAs detected by massively parallel sequencing	Sem 1
11:30-12:00	Coin, L (Imperial College London)
	Integration of sequence and array data in a population and haplotype-based model of SNPs and CNVs	Sem 1
12:00-12:30	McCarroll, S (Harvard University)
	Population-based analysis of genome structural variation using broad, highly parallel population sequencing	Sem 1
16:00-16:30	Parkhill, J (Wellcome Trust Sanger Institute)
	Population genomics of bacterial pathogens	Sem 1
16:30-17:00	Falush, D (University College Cork)
	Microevolutionary analysis of metagenomic data	Sem 1
17:00-17:30	Kwiatkowski, D
	Using next-gen sequencing to get at the genetic architecture and dynamics of Plasmodium falciparum populations	Sem 1

Friday 16 July
09:30-10:00	Pastinen, T (McGill University)
	Cis-regulatory SNPs (cis-rSNPs) altering transcription detected by allelic expression (AE) mapping	Sem 1
10:00-10:30	Plagnol, V (University College London)
	Allele specific expression analysis using high throughput DNA sequencing	Sem 1
10:30-11:00	Taylor, J (CSIRO)
	Genome-wide characteristics of sequence coverage by next-generation sequencing: how does this impact interpretation?	Sem 1
11:30-12:00	Gottardo, R (University of British Columbia)
	A statistical framework for the analysis of ChIP-Seq data	Sem 1
12:00-12:30	Odom, D (University of Cambridge)
	Species specific transcription in mice carrying human chromosome 21	Sem 1
12:30-13:00	Park, P (Harvard University)
	Identification of enriched regions in ChIP-seq and whole-genome sequencing data	Sem 1

Tuesday 03 August
14:00-14:40	Bentley, D (Illumina)
	Should I sequence my genome now?	Sem 1
14:40-15:20	Carter, N (Wellcome Trust Sanger Institute)
	DECIPHER and opportunities and challenges for clinical genetics of next gene sequencing	Sem 1
15:20-16:00	Nelson, M (GlaxoSmithKline)
	Prospects for pharmacogenetics in a genome-sequencing era	Sem 1
16:30-17:15	McVean, G (Oxford)
	The 1000 Genomes Project and challenges in population-scale sequencing	Sem 1
17:15-18:15
	Panel Discussion	Sem 1

Other Seminars

Seminars in the University National and International Scientific Research Meetings

© Isaac Newton Institute

Updated at 10:06 AM on 27 February 2013