441. Mason
A fast, feature-rich and hackable read simulator for the simulation of NGS and Sanger data.
标签:Genomics
442. PoissonSeq
Identify differential expressed genes
标签:Differential Expression
443. CATCH
A tool for exploring patterns in ChIP profiling data.
标签:ChIP-Seq, ChIP-on-chip
444. Genomedata
Genomedata is a format for efficient storage of multiple tracks of numeric data anchored to a genome. The format allows fast random access to hundreds of gigabytes of data, while retaining a small disk space footprint.
标签:Storage
445. Vectorfriends
VectorFriends is an advanced, integrated, and user-friendly sequence analysis software for molecular biologists. It combines various types of in silico cloning, sequence analysis and data management into a single application.
标签:
446. UGENE
UGENE is a free cross-platform genome analysis suite that combines popular bioinformatics tools within a single user friendly interface.
标签:Phylogenetics, Genomics,Sequence analysis, Protein structure analysis
447. SPP
R-scripts for ChIP-seq analysis.
标签:Genomics, ChIP-Seq
448. RDP Pyrosequencing Pipeline
The Ribosomal Database Project's Pyrosequencing Pipeline aims to simplify the processing of large 16s rRNA sequence libraries obtained through pyrosequencing. This site processes and converts the data to formats suitable for common ecological and statistical packages such as SPADE, Esti...
标签:Metagenomics
449. SeqGSEA
Gene Set Enrichment Analysis (GSEA) of RNA-Seq Data: integrating differential expression and splicing
标签:Biomedical Sciences, Genomics,RNA-Seq
450. Arf
arf is a genetic analysis program for sequencing data.
标签:
451. SUDS genome browser
Compressed suffix tree implementation to browser genome sequences
标签:
452. Genomatix Mining Station (GMS)
The Genomatix Mining Station (GMS) offers mapping of NGS reads onto genomes, transcriptomes and splice-junction libraries. It is a client-server based solution and can be controlled through an intuitive GUI or via command-line. It covers different tasks such as, as genomic positioning, ...
标签:RNA-Seq, SNP discovery, ChIP-Seq
453. SpliceGrapher
SpliceGrapher is a package for creating splice graphs from RNA-Seq data, guided by gene models and EST data (when available).
标签:Alternative Splicing
454. Ngs backbone
ngs_backbone is a bioinformatic application created to work on sequence analysis by using NGS (Next Generation Sequencing) and sanger sequences. It is capable of cleaning reads, do de novo assembly or mapping against a reference and annotate SNPs, SSRs, ORFs, GO terms and sequence descr...
标签:SNP discovery, Genomics
455. Flux
FluxCapacitor s a computer program to predict splice form abundancies from reads of an RNA-seq experiment. FluxSimulator can generate simulated data for testing RNA-seq pipelines
标签:RNA-Seq
456. WebPrInSeS
WebPrInSeS encompasses two separate software applications. The first is WebPrInSeS-C which performs automated sequence verification of user-defined open-reading frame (ORF) clone libraries. The second is WebPrInSeS-E, which identifies positive hits in cDNA or ORF-based library screening...
标签:Clone verification, Yeast two-hybrid, Yeast one-hybrid
457. DNA Chromatogram Explorer
DNA Chromatogram Explorer is a Windows Explorer clone dedicated to DNA sequence analysis and manipulation.
标签:
458. Subjunc
The Subread read aligner and Subjunc junction detector employ a novel read mapping paradigm called "seed-and-vote" to achieve a fast mapping speed and a high mapping accuracy. The seed-and-vote paradigm is particularly powerful in detecting indels. Subjunc can be used to discover exon-e...
标签:Alternative Splicing, Next-generation sequencing, RNA-Seq Alignment
459. LASTZ
A tool for (1) aligning two DNA sequences, and (2) inferring appropriate scoring parameters automatically
标签:Genomics
460. Readaligner
A tool for mapping (short) DNA reads into reference sequences.
标签: