581. Isas
Fast aligner for color and base space short read data.
标签:
582. JBrowse
Slick, speedy genome browser with a responsive and dynamic AJAX interface for visualization of genome data. Being developed by the GMOD project as a successor to GBrowse.
标签:
583. KARMA
K-tuple Alignment with Rapid Matching Algorithm
标签:Bisulfite Sequencing
584. KBASE
"KBase provides a computational framework and tools for integrating and analyzing large, diverse datasets generated by the scientific community to advance predictive understanding, manipulation, and design of biological processes in an environmental context. The purpose of KBase is to e...
标签:Comparative genomics
585. Lab7
Data workflow management platform to streamline NGS analyses
标签:Genomics
586. MagicViewer
Large-scale short reads and sequencing depth visualization.
标签:De novo sequencing, Targeted resequencing
587. mapsembler
Mapsembler is a targeted assembly software. It takes as input a set of NGS raw reads and a set of input sequences (starters). It first determines if each starter is read-coherent, e.g. whether reads confirm the presence of each starter in the original sequence. Then for each read-cohere...
标签:Metagenomics, Transcriptomics,DNA-Seq, RNA-Seq Quantitation,Targeted assembly
588. MAXIMUS
Hybrid reference and de novo assembly pipeline
标签:Genomics
589. Meerkat
Meerkat is designed to identify structure variations (SVs) from paired end high throughput sequencing
标签:Structural variation
590. MeV
Visualization of genomic data, Differential Gene Expression based on DEGseq, DESeq and edgeR
标签:RNA-Seq
591. Microsoft Biology Foundation
C#/.NET library for biological applications.
标签:
592. Minia
De novo assembly of human genomes on a desktop computer
标签:De novo assembly
593. MIP Scaffolder
MIP Scaffolder is a program for scaffolding contigs produced by fragment assemblers using mate pair data.
标签:
594. MiRProf
Determines normalised expression levels of sRNAs matching known miRNAs in miRBase.
标签:General bioinformatics (pipeline)
595. MiRspring
missing
标签:
596. MochiView
Hybrid genome browser and motif visualization/analysis/management desktop software.
标签:Genomics, ChIP-Seq, ChIP-on-chip, RNA-Seq, Motif analysis
597. MOSAIK
Reference guided aligner/assembler.
标签:
598. MrBayes
"MrBayes is a program for Bayesian inference and model choice across a wide range of phylogenetic and evolutionary models. MrBayes uses Markov chain Monte Carlo (MCMC) methods to estimate the posterior distribution of model parameters." Program for the Bayesian estimation of phylogeny.
标签:Phylogenetics
599. MrCaNaVaR
mrCaNaVaR is a copy number caller that analyzes the next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals.
标签:Genomics, Personal genomics,Copy number estimation
600. MuSICA 2
Assembles millions of short (36-nucleotide) reads collected from a single flow cell lane of Illumina Genome Analyzer to shotgun-sequence ~800 human full-length cDNA clones.
标签:Clone verification