'Gen sequencing' presentation slideshows

Vince Buonaccorsi Associate Professor of Biology Juniata College

NextGen sequencing for undergraduate research and curriculum. Vince Buonaccorsi Associate Professor of Biology Juniata College. NextGen Sequencing Technologies 454 Sequencing (Roche) SOLiD Sequencing (ABI). Nextgen sequencing: How it works. 454 GS FLX Titanium Series.

886 views • 76 slides

BIONF/BENG 203: Functional Genomics

BIONF/BENG 203: Functional Genomics. Lecture TI 1,2 Trey Ideker UCSD Departments of Medicine & Bioengineering. Sources of Functional Data Lectures 1 and 2. 1. Instructors. Trey Ideker Vineet Bafna Anand Patel (TA). Grading. 40% Problem Sets (best 4 of 5) 30% Midterm 30% Final Project.

604 views • 60 slides

Chem 395 Bioanalytical Chemistry Storrs, Connecticut February 8, 2011

Chem 395 Bioanalytical Chemistry Storrs, Connecticut February 8, 2011. Modern Genomic Analysis Methods Janet Hager Translational Genomics Core Department of Genetics and Developmental Biology University of Connecticut Health Center. Genomic Resources at the UCHC Translational Genomics Core.

503 views • 50 slides

A better clinical pathway for cancer monitoring

A better clinical pathway for cancer monitoring. Antonius Schuh, Ph.D. | Chief Executive Officer September 2013.

425 views • 34 slides

Final

Final. Thursday May 22, 2014 Take home No help 10% extra credit Due Monday May 26, 2013 at midnight Submit to gene210.stanford@gmail.com. Discovery of new Mendelian disorders by Next Gen sequencing. Strategy. Syndrome Full Genome Sequence Look for coding mutations.

401 views • 32 slides

Final

Final. Thursday May 22, 2014 Take home No help 10% extra credit Due Monday May 26, 2013 at midnight Submit to gene210.stanford@gmail.com. Discovery of new Mendelian disorders by Next Gen sequencing. Strategy. Syndrome Full Genome Sequence Look for coding mutations.

378 views • 32 slides

Fitness landscapes; LTEE

420 views • 29 slides

Detecting copy number variations using paired-end sequence data

Detecting copy number variations using paired-end sequence data. CS224 May 29, 2009. Nick Furlotte. SNPs are old news. SNPs have been the main way of quantifying genetic variation Attention is now switching to other harder to detect variations

342 views • 20 slides

The Genome Center Washington University School of Medicine

GBM Mutation Analysis and New Sequencing Technologies. Richard K. Wilson, Ph.D. The Genome Center Washington University School of Medicine. Targeted re-sequencing in TCGA. ~1500 genes of interest. ~200 GBM tumors (& matching normals). Sequencing Centers: BCM-HGSC, BI, WUGSC

303 views • 14 slides

222 views • 11 slides

SIGNAL PROCESSING FOR NEXT-GEN SEQUENCING DATA

Peaks. DNAse I- seq. CHIP- seq. SIGNAL PROCESSING FOR NEXT-GEN SEQUENCING DATA. Gene models. RNA- seq. Binding sites. RIP/CLIP- seq. FAIRE- seq. Transcripts. The Power of Next-Gen Sequencing. Chromosome Conformation Capture. + More Experiments. DNA Genome Sequencing

197 views • 9 slides