Results for "MinION. NGS"
Bookmarks
DAVI: Deep learning-based tool for alignment and single nucleotide variant identification
DAVI consists of models for both global and local alignment and for variant calling. We...ology, the models proposed in DAVI are generic and can be used across different NGS technologies as well as acros...1139 days ago
Next Generation Sequencing (NGS) Tutorials
Institute of computational biomedicin...Cornell University provide an NGS workshop tutorial at http://chagall.med.cornell.edu/NGScourse/ You can also ad...0.1093/bioinformatics/btr441 ngs_backbone: a pipeline for read...ic-phd-school/course-schedule/ngsmetagenomics/ RNASeq:http://w...3480 days ago
Orione – a web-based framework for NGS analysis in microbiology
End-to-end NGS microbiology data analysis requires a diversity of...lines to build complex, reproducible workflows for NGS microbiology data analysis. E...Fotia G. (2014) Orione, a web-based framework for NGS analysis in microbiology. Bio...3567 days ago
Next generation sequencing(NGS) books
Employing different technologies, the purpose of NGS platform is to decode the identity or modification on the nucleotides. NGS platforms evolve quickly and capture the main stream. This bookmark is created to provide NGS online books links.3621 days ago
Bioinformatics algorithms tutorials
Useful bioinformatics tutorial, such as De Bruijn Graphs for NGS AssemblyAlgorithms for PacBio ReadsSoftware and Hardware Concepts for BioinformaticsFinding us in Homolog.us (Search Algorithms)NGS Genome and RNAseq Assembly -...3596 days ago
Integrative Genomics Viewer (IGV) tutorial
The Integrative Genomics Viewer (IGV) from the Broad Center allows you to view several types of data files involved in any NGS analysis that employs a refer...3577 days ago
COSMOS, our workflow management system for NGS data
COSMOS, our Python-based management system for implementing large-scale parallel workflows focusing on, but not restricted to, large-scale short-read "NGS" sequencing data is open-acce...3567 days ago
- LASTZ is a program for aligning DNA sequences, a pairwise aligner. Originally designed...mosomes and from different species, it is also useful for sequences produced by NGS sequencing technologies such...
2932 days ago
- You are requested to please bookmark collection of bioinformatics tools, scr...nity. https://code.google.com/p/biowiki/ https://code.google.com/p/ngs-pipeline/source/browse/#svn%2Ftrunk NGSand Perl scripts https://code....
3227 days ago
GraphMap - A highly sensitive and accurate mapper for long, error-prone reads
GraphMap is a novel mapper targeted at aligning long, error-prone third-generation sequencing data.It is designed to handle Oxford Nanopore MinION 1d and 2d read...3217 days ago
