281. MAQGene
Complete pipeline for mutant discovery, with web front end
标签:SNP discovery
282. PICS
PICS identifies binding event locations by modeling local concentrations of directional reads, and uses DNA fragment length prior information to discriminate closely adjacent binding events via a Bayesian hierarchical t-mixture model.
标签:ChIP-Seq
283. RAPSearch
Fast protein similarity search tool for short reads that utilizes a reduced amino acid alphabet and suffix array to detect seeds of flexible length.
标签:Metagenomics
284. ConDeTri
ConDeTri is a content dependent read trimming software for Illumina/Solexa sequencing data
标签:RNA-Seq, DNA-Seq, Genomics
285. PALMA
We present a novel approach based on large margin learning that combines accurate splice site predictions with common sequence alignment techniques. By solving a convex optimization problem, our algorithm -- called PALMA -- tunes the parameters of the model such that true alignments sco...
标签:RNA-Seq Alignment
286. Sim4cc
Cross-species spliced alignment of ESTs to genomes
标签:RNA-Seq Alignment, Comparative genomics
287. FusionMap
Detects fusion events in both single- and paired-end datasets from either RNA-Seq or gDNA-Seq studies and characterize fusion junctions at base-pair resolution.
标签:Fusion genes, Fusion transcripts
288. ISSAKE
Short Sequence Assembly by K-mer search and 3' read Extension, Immunology version (iSSAKE)
标签:Metagenomics
289. GBrowse
Genome Viewer Visualisateur de génomes accessible par le web.
标签:
290. VIP
A complete package designed for next-generation diagnostics using 454 sequencing.
标签:Genomics, SNP discovery, SNP Annotation
291. Btrim
Btrim is a fast and lightweight software to trim adapters and low quality regions in reads.
标签:
292. JointSLM
Copy number estimation from read depth information
标签:Copy number estimation
293. Girafe
The R/Bioconductor package girafe facilitates the functional exploration of alignments of sequence reads from next-generation sequencing data to a genome. It allows users to investigate the genomic intervals together with the aligned reads and to work with, visualise and export these in...
标签:
294. RApiD
Tools for processing restriction site associated DNA sequencing.
标签:SNP discovery
295. SeqCons
SeqCons is an open source consensus computation program for Linux and Windows. The algorithm can be used for de novo and reference-guided sequence assembly.
标签:
296. HI
Program for haplotype reconstruction from paired-end reads.
标签:
297. EMBF
Frequency-based, de novo short-read clustering method that organizes erroneous short sequences originating in a single abundant sequence into a tree structure; in this structure, each “child” sequence is considered to be stochastically derived from its more abundant “parent” sequence wi...
标签:
298. GENE-Counter
GENE-counter is a computational pipeline for analyzing RNA-Sequencing (RNA-Seq) data for differential gene expression
标签:RNA-Seq
299. TASR
Targeted assembly of short read data to identify the presence of variants
标签:Targeted assembly
300. MethMarker
MethMarker facilitates the design of DNA methylation assays for COBRA, bisulfite SNuPE, bisulfite pyrosequencing, MethyLight and MSP. It also implements a systematic workflow for design, optimization and (computational) validation of DNA methylation biomarkers. This workflow starts from...
标签:Epigenomics, DNA methylation