321. SEAL
Read mapper and duplicate remover.
标签:
322. FusionAnalyser
FusionAnalyser is a new graphical, event-driven tool dedicated to the identification of driver fusion rearrangements in human cancer through the analysis of paired-end high-throughput transcriptome sequencing data. Tested on Illumina. Requires short, paired-end sequences.
标签:High-throughput sequencing
323. ArrayStar
ArrayStar is an easy-to-use gene expression analysis software package that offers powerful visualization and statistical tools to help you analyze your microarray data.
标签:Gene Expression Analysis
324. PileLine
PileLine is a flexible command-line toolkit for efficient handling, filtering, and comparison of genomic position (GP) files produced by next-generation sequencing experiments. PileLineGUI adds a graphical interface.
标签:
325. MAYDAY
Extensible platform for visual data exploration and interactive analysis and provides many methods for dissecting complex transcriptome datasets.
标签:RNA-Seq
326. LOCAS
LOCAS low-coverage short-read assembler
标签:
327. SlideSort
SlideSort finds all similar pairs from a string pool in terms of edit distance. Using an efficient pattern growth algorithm, SlideSort discovers chains of common k-mers to narrow down the search.
标签:
328. Bis-SNP
BisSNP is a package based on the Genome Analysis Toolkit (GATK) map-reduce framework for genotyping in bisulfite treated massively parallel sequencing (Bisulfite-seq, NOMe-seq and RRBS) on Illumina platform. It uses bayesian inference with either manually specified or automatically esti...
标签:SNP discovery, Genotyping, DNA methylation, Bisulfite Sequencing
329. PiCall
Identifies short indel polymorphisms in population sequencing data
标签:InDel discovery, Population genetics
330. SR-ASM
SR-ASM algorithm is designed for DNA assembly of the short sequences coming from 454 sequencers.
标签:De-novo assembly
331. DecGPU
Parallel and distributed error correction algorithm for high-throughput short reads.
标签:De-novo assembly
332. PALMapper
Fast and Accurate Spliced Alignments of Sequence Reads.
标签:
333. CloudAligner
Hadoop-based short read aligner
标签:
334. R453Plus1Toolbox
Facilitates analysis of data from 454 sequencer in R/Bioconductor.
标签:
335. MapNext
MapNext provides four mainly analysis: (i) unspliced alignment and clustering of reads, (ii) spliced alignment of transcriptomic reads, (iii) SNP detection and calculation of SNP frequency from population sequences, and (iv) storage of result data into database to make it available for ...
标签:SNP discovery, RNA-Seq Alignment
336. BFCounter
BFCounter is a program for counting k-mers in DNA sequence data.
标签:
337. Pybedtools
Python extension to BEDTools that allows use of all BEDTools programs directly from Python, as well as feature-by-feature manipulation, automatic handling of temporary files, and more.
标签:Genomics
338. SESAME
Gnotyping of multiplexed individuals for several markers based on NGS amplicon sequencing.
标签:Genotyping, Targeted resequencing
339. VARiD
VARiD is a variation detection framework for both color-space and letter-space platforms
标签:Genomics, SNP discovery, InDel discovery
340. RNASEQR
a streamlined and accurate RNA-seq sequence analysis program
标签:Alternative Splicing