Results for "Strand 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. W...ology, the models proposed in DAVI are generic and can be used across different NGS technologies as well as acros...1130 days ago
Next Generation Sequencing (NGS) Tutorials
Institute of computational biomedici...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...3471 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...3558 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.3612 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 -...3588 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...3569 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...3558 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...
2923 days ago
- You are requested to please bookmark collection of bioinformatics tools, scr...unity. https://code.google.com/p/biowiki/ https://code.google.com/p/ngs-pipeline/source/browse/#svn%2Ftrunk NGSand Perl scripts https://code....
3218 days ago
RACA: Reference-Assisted Chromosome Assembly
Rreference-Assisted Chromosome Assembly (RACA), an algorithm to reliably order and orient sequence scaffolds generated by NGS and assemblers into longer ch...2935 days ago
