Switching between raltegravir resistance pathways analyzed by deep sequencing Rithun Mukherjeea, Shane T. Jensenb, Frances Malea, Kyle Bittingera, Richard L. Hodinkac,d, Michael D. Millere and Frederic D. Bushmana Object

Source URL: www-stat.wharton.upenn.edu

  Workshop Title: ​ Whole Exome Sequencing Data Analysis Workshop venue: Department of Biochemistry and Biotechnology, College of Science, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana

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Next-generation sequencing can replace Sanger sequencing in clinical diagnostics. Birgit Sikkema-Raddatz Department of Genetics, University Medical Center Groningen The Netherlands

Source URL: www.molekularediagnostik.ch

Phase 4: Variant prioritisation Even with sound experimental design and variant filtering protocols, whole exome sequencing studies often still produce many more candidates than can be verified experimentally. While pos

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Improving the Power of Rare-Variant Association Tests by a Position-Dependent Kernel Approach Ulrich Bodenhofer and Sepp Hochreiter Current high-throughput sequencing technologies have allowed for an easy and cost-effici

Source URL: www.bioinf.jku.at

Procedure & Checklist - 10 to 20 kb Template Preparation and Sequencing with Low (100 ng) Input DNA

Source URL: www.pacb.com

Postdoctoral Position in Nanobiotechnology Seeking a Ph.D to support research projects in nano-biotechnologies such as single molecule spectroscopy with either scanned probe microscopy or optical tweezers; sequencing p

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Template Preparation FIND MEANING IN COMPLEXITY © Copyright 2014 by Pacific Biosciences of California, Inc. All rights reserved. PN Specifics of SMRT® Sequencing Data

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Handling Long Targets and Errors in Sequencing by Hybridization Eran Halperin ABSTRACT   

Source URL: www.cs.tau.ac.il

Molecular Ecology, 2310–2323 doi: mecINVITED REVIEWS AND SYNTHESES

Source URL: palumbi.stanford.edu

• Biology
• Molecular biology
• Genetics
• RNA-Seq
• De novo transcriptome assembly
• Sequence assembly
• DNA sequencing
• Transcriptome
• Single-nucleotide polymorphism
• Expressed sequence tag
• Bioinformatics
• Contig