21. Epigenome
A bioinformatic pipeline that scores epigenetic alterations according to strength and significance and links them to potentially affected genes.
标签:Epigenomics
22. LAST
Short read alignment program incorporating quality scores
标签:Genomics, Comparative genomics
23. SSPACE
Stand-alone scaffolder of pre-assembled contigs using paired-read data. SSPACE standard is a stand-alone program for scaffolding pre-assembled contigs using NGS paired-read data.
标签:Genomics
24. CloudBurst
CloudBurst is a parallel read-mapping algorithm optimized for mapping next-generation sequence data to the human genome and other reference genomes.
标签:SNP discovery, Genotyping,Personal genomics
25. MoDIL
Program to detect small indels in next generation sequencing data
标签:Genomics, InDel discovery
26. MrsFAST
mrsFAST is a micro-read substitution-only Fast Alignment Search Tool. mrsFAST is a cache-oblivous short read mapper that optimizes cache usage to get higher performance.
标签:Genomics
27. Segemehl
Map short reads to known genome with tolerance for mismatches and indels using suffix arrays for high accuracy matching
标签:Genomics
28. ShoRAH
Inference of a population from a set of short reads. The package contains programs that support mapping of reads to a reference genome, correcting sequencing errors by locally clustering reads in small windows of the alignment, reconstructing a minimal set of global haplotypes that expl...
标签:Metagenomics
29. NPS
Identify nucleosome positions given histone-modification ChIP-seq or nucleosome sequencing at the nucleosome level.
标签:Epigenomics, ChIP-Seq
30. MUMmerGPU
MUMmerGPU is a low cost, ultra-fast sequence alignment program designed to handle the increasing volume of data produced by HTS.
标签:Genomics, Transcriptomics
31. SeqAn
C++ template library with many sequence analysis algorithms and datastructures.
标签:Sequence analysis, Genomics,Phylogenetics
32. BS Seeker
Mapping tool for bisulfite treated reads
标签:Epigenomics
33. Prinseq
PRINSEQ is a sequence processing tool that can be used to filter, reformat and trim genomic and metagenomic sequence data. It generates summary statistics of the input in graphical and tabular formats that can be used for quality control steps. PRINSEQ is available as both standalone an...
标签:Metagenomics, Genomics,Metatranscriptomics
34. FragGeneScan
Application for finding (fragmented) genes in short reads
标签:Metagenomics
35. Bismark
Bismark is a tool to map bisulfite treated sequencing reads and perform methylation calling in a quick and easy-to-use fashion.
标签:Epigenomics, Genomics, DNA methylation
36. Novocraft
Novoalign is a program for mapping short reads from the Illumina/SOLiD sequencing platform(s) to a reference genome. Package for aligning short reads to reference genomes
标签:Genomics, Whole Genome Resequencing, RNA-Seq Alignment, ChIP-Seq, MiRNA
37. Savant Genome Browser
Savant is a genome browser which combines visualization of HTS and other genome-based data with powerful analytic tools.
标签:Genomics
38. PerM
PerM (Periodic Seed Mapping) uses periodic spaced seeds to significantly improve mapping efficiency for large reference genomes when compared to state-of-the-art programs.
标签:Genomics, SNP discovery
39. RSAT peak-motifs
A workflow combining a series of time- and memory-efficient motif analysis tools to extract motifs from full-size collections of peaks as generated by ChIP-seq, ChIP-chip or other ChIP-X technologies.
标签:ChIP-Seq, Regulatory genomics,Epigenomics
40. Kismeth
Web-based tool for bisulfite sequencing analysis
标签:DNA methylation, Epigenomics