Results for "Deep Sequencing"
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Sequencing Solutions to World Health
"New technology that quickly, easily and economically reveals the genomes of viruses and pathogens transforms public health and medicine." Source: Life technologies3901 days ago
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...onstrate that while existing tools are based on data generated from a specific sequencing technology, the models propos...1145 days ago
Comparison of Short Read De Novo Alignment Algorithms
Excellent article to introduce different sequencing methods along with tools for de novo assembly of sequencing reads and their relevant references. Title: Comparison of Short Read De Novo Alignment Algorithms Author: Nikhil Gopal3909 days ago
Statistics of current Sequencing and Bioinformatics market
This survey conducted by Oxford Gene Tec...recent survey of researchers using next generation sequencing. (Source:http://www.news-medi...21/Oxford-Gene-Technology-releases-next-generation-sequencing-survey-results.aspx ) &...3909 days ago
Illuminating next generation sequencing data with Go
Another good lecture for Illumina sequencing data analysis from Dan Kortschak, Bioinformatics Group, School of Molecular and Biomedical Science ,The University of Adelaide3907 days ago
Next Generation Sequencing (NGS) Tutorials
Institute of computational biomedicine, C...Understanding the basics of genome sequencing: Tutorial by Luke Jostins....-inference.co.uk/blog/2009/04/basics-sequencing-dna-part-1/ http://www.genet...genotyping using next-generation DNA sequencing data PubMed: 21478889...3487 days ago
RNA Sequencing Helps Identify Functional Variants from GWAS
For Alzheimer’s and other complex disorders, mining the genome for disease-as...t month in Nature and its associated journals, advances in high-throughput RNA sequencing are providing new tools for u...3815 days ago
Janggu - Deep learning for Genomics
Janggu is a python package that facilitates deep learning in the context of genomics. The package is freely available under a GPL-3.0 license. Detail tutorial at https://janggu.readthedocs.io/en/latest/ USE cases https://github.com/wkopp/janggu_usecases1138 days ago
Bioinformatics software for biologists in the genomics era
The genome sequencing revolution is approaching a landmark figure of 1000 completely sequenced genomes. Coupled with fast-declining, per-base sequencing costs, this influx of DNA seq...3786 days ago
Encode sequencing data freely available to download and use for academic means
In Encode, regulatory elements investigated via DNA hypersensitivity assays, a...t with DNA, including modified histones and transcription factors, followed by sequencing (ChIP-Seq). More information...3705 days ago
