QReadSelector is a subset selection of high-depth next generation sequencing reads for de novo genome assembly using MapReduce framework.
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Updated
Aug 26, 2015 - Java
QReadSelector is a subset selection of high-depth next generation sequencing reads for de novo genome assembly using MapReduce framework.
A course on Analysing Next Generation (/High Throughput etc..) Sequencing data using Bioconductor
Genome-Wide RNA Degradation Analysis Using BRIC-Seq Data
software for processing tuberculosis whole genome data. interface to the BWA, VarScan, SamTools etc.
Resequencing project for Fusarium graminearum
Some DataStructures specialized for working with NGS data.
A buggier version of [Bio.jl](https://github.com/BioJulia/Bio.jl) with less features and worse performance.
RNA Fusion Detection Using STAR. (aka starseqr)
(Archived) This page is a record of my first formal NGS Project for Dr. Matesic of University of South Carolina (USC).
A front-end GUI to map NGS DNA sequencing data using HISAT backend tool. This software offers robust seamless queueing of the mapping operations along with parameter memory for quick and easy customization.
Small tool to simulate AdapterContamination of NGS reads and evaluate the findings afterwards.
NanoString classifier based on NGS training set
A scripts used to check the NGS (Next-generation sequencing) raw data quality of fastq formated files, similar to FastQC.
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