1. GenomeView
GenomeView is a next-generation stand-alone genome browser and editor initiated in the BSB group at VIB and currently developed at Broad Institute. It provides interactive visualization of sequences, annotation, multiple alignments, syntenic mappings, short read alignments and more. Man...
标签:Genomics, Comparative genomics, Comparative transcriptomics,Transcriptomics, Gene annotation retrieval, Quality Control, Sequencing, Sequence analysis
2. QUAST
QUAST stands for QUality ASsessment Tool. It evaluates a quality of genome assemblies by computing various metrics and providing nice reports.
标签:Quality Control, Genomic Assembly Evaluation, Sequence analysis
3. Error Correction Evaluation Toolkit
Evaluation of error correction results
标签:Sequence Quality Control
4. BBMap
BBMap is a fast splice-aware aligner for RNA and DNA. It is faster than almost all short-read aligners, yet retains unrivaled sensitivity and specificity, particularly for reads with many errors and indels.
标签:Resequencing, Alignment,Quality Control, RNA-Seq Alignment, Alternative Splicing, Whole Genome Resequencing, SNP discovery,Phylogenetics, Metagenomics,Read Binning
5. QualiMap
Qualimap is a platform-independent application written in Java and R that provides both a Graphical User Inteface (GUI) and a command-line interface to facilitate the quality control of alignment sequencing data.
标签:Sequence Quality Control,Quality Control
6. Standardized Velvet Assembly Report
A set of scripts and a Sweave report used to iterate through parameters and generate a report on Velvet-generated sequence assemblies
标签:Quality Control
7. FastQValidator
Checking that FastQ files are follows standards
标签:Quality Control
8. Flexbar
flexible barcode and adapter processing for next-generation sequencing platforms
标签:Next Generation Sequencing,Sequence Quality Control,Genomics
9. Golden Helix
Golden Helix is a bioinformatic software provider and analytic service provider. The core of its business is about empowering scientists to discover more, discover it easier, and to come away with valid and reproducible bioinformatics results. The software, SNP & Variation Suite, is a s...
标签:Epigenomics, Genomics, DNA-Seq, SNP discovery, Whole Genome Resequencing Analysis,Copy number estimation,Quality Control
10. Spiral Genetics
Spiral Genetics provides a novel aligner/variant caller, Anchored Assembly, which can detect large structural variations using short read NGS data with unmatched precision.
标签:Alignment, DNA-Seq, Exome and Whole genome variant detection, De novo Assembly,Genomic Assembly, Mapping,Quality Control, Read alignment, Reference assembly,Resequencing, SNP discovery,Sequence analysis, Whole Genome Resequencing