61. SEED
Tool to cluster sequence reads prior to assembly or other operations.
标签:Metagenomics
62. ChromHMM
ChromHMM is software for learning and characterizing chromatin states.
标签:Epigenomics
63. Krona
Krona creates interactive HTML5 charts of hierarchical data (such as taxonomic abundance in a metagenome).
标签:Metagenomics
64. 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
65. ConDeTri
ConDeTri is a content dependent read trimming software for Illumina/Solexa sequencing data
标签:RNA-Seq, DNA-Seq, Genomics
66. Sim4cc
Cross-species spliced alignment of ESTs to genomes
标签:RNA-Seq Alignment, Comparative genomics
67. ISSAKE
Short Sequence Assembly by K-mer search and 3' read Extension, Immunology version (iSSAKE)
标签:Metagenomics
68. VIP
A complete package designed for next-generation diagnostics using 454 sequencing.
标签:Genomics, SNP discovery, SNP Annotation
69. 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
70. BRCA-diagnostic
Computational screening test for BRCA1/2 mutants in human genomic DNA
标签:Personal genomics
71. FACS
Rapid and accurate classification of sequences as belonging or not belonging to a reference sequence.
标签:Metagenomics
72. ABMapper
Maps RNA-Seq reads to target genome considering possible multiple mapping locations and splice junctions
标签:Genomics, Transcriptomics
73. Metaxa
Metaxa uses Hidden Markov Models to identify, extract and classify small-subunit (SSU) rRNA sequences (12S/16S/18S) of bacterial, archaeal, eukaryotic, chloroplast and mitochondrial origin in metagenomes and other large sequence sets
标签:Metagenomics, Phylogenetics,Sequence analysis, Community analysis
74. NucleR
nucleR is a R/Bioconductor package for working with tiling arrays and next generation sequencing. It uses a novel aproach in this field which comprises a deep profile cleaning using Fourier Transform and peak scoring for a quick and flexible nucleosome calling
标签:ChIP-on-chip, ChIP-Seq,Nucleosome Positioning,Epigenomics
75. GenomeView
GenomeView is a next-generation stand-alone genome browser and editor initiated in the BSB group at VIB and currently developed at Broad Institute. It provides interactive visualization of sequences, annotation, multiple alignments, syntenic mappings, short read alignments and more. Man...
标签:Genomics, Comparative genomics, Comparative transcriptomics,Transcriptomics, Gene annotation retrieval, Quality Control, Sequencing, Sequence analysis
76. CatchAll
Estimate ecological diversity with both parametric and non-parametric estimators.
标签:Population genetics,Metagenomics
77. 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
78. VARiD
VARiD is a variation detection framework for both color-space and letter-space platforms
标签:Genomics, SNP discovery, InDel discovery
79. CNANorm
A normalization method for Copy Number Aberration in cancer samples.
标签:Cancer biology, Copy number estimation, Genomics
80. GenomicTools
GenomicTools is a flexible computational platform for the analysis and manipulation of high-throughput sequencing data such as RNA-seq and ChIP-seq. A variety of mathematical operations between sets of genomic regions is implemented thereby enabling the prototyping of computational pipe...
标签:Genomics, ChIP-Seq, RNA-Seq