361. AREM
AREM: Aligning Short Reads from ChIP-Sequencing by Expectation Maximization
标签:ChIP-Seq
362. ExomeCopy
CNV detection from exome sequencing read depth
标签:Exome and Whole genome variant detection, Copy number estimation, Exome analysis
363. RiboPicker
riboPicker is a publicly available tool that is able to automatically identify and efficiently remove rRNA-like sequences from metatranscriptomic and metagenomic datasets. riboPicker is available as both standalone and web-based versions.
标签:Metagenomics, Genomics,Metatranscriptomics
364. MU2A
Genomic variant annotation tool
标签:SNP Annotation
365. PoolHap
Computational tool for inferring haplotype frequencies from pooled samples when haplotypes are known. In future version, haplotype unknown analysis will be supported.
标签:
366. QUAST
QUAST stands for QUality ASsessment Tool. It evaluates a quality of genome assemblies by computing various metrics and providing nice reports.
标签:Quality Control, Genomic Assembly Evaluation, Sequence analysis
367. Segtor
A software tool to annotate large sets of genomic coordinates, intervals, SNVs, indels and translocations with respect to known genes.
标签:SNP Annotation
368. Megraft
Megraft is a software tool to graft ribosomal small subunit (16S/18S) fragments from metagenomes onto full-length SSU sequences, enabling accurate diversity estimates from fragmentary and non-overlapping sequence data.
标签:Metagenomics, Phylogenetics,Sequence analysis, Community analysis, Rarefaction
369. FAAST
Flowspace Assisted Alignment Search Tool
标签:
370. Breakpointer
Breakpointer is a fast tool for locating sequence breakpoints from the alignment of single end reads (SE) produced by next generation sequencing (NGS). It adopts a heuristic method in searching for local mapping signatures created by insertion/deletions (indels) or more complex structur...
标签:Exome and Whole genome variant detection, InDel discovery
371. GEM
GEM is a java software tool to analyze transcription factor binding ChIP-Seq/ChIP-exo data. It predicts binding events, performs de novo motif discovery and use the motif to improve the binding event calling. It calls binding events right at (or very close to ) the motif positions, deco...
标签:ChIP-Seq
372. Seq2HLA
seq2HLA is a computational tool to determine Human Leukocyte Antigen (HLA) directly from existing and future short RNA-Seq reads. It takes standard RNA-Seq sequence reads in fastq format as input, uses a bowtie index comprising known HLA alleles and outputs the most likely HLA class I a...
标签:Transcriptomics
373. Patchwork
Patchwork is a bioinformatic tool for analyzing and visualizing allele-specific copy numbers and loss-of-heterozygosity in cancer genomes. The data input is in the format of whole-genome sequencing data which enables characterization of genomic alterations ranging in size from point mut...
标签:Structural variation
374. Bort
Bort parses Blast output and quantifies hits by contig and read counts.
标签:RNA-Seq Quantitation
375. GeeFu
Database tool for genomic assembly and feature data
标签:Genomics
376. Quip
Aggressive compression of FASTQ and SAM/BAM files.
标签:
377. BING
biomedical informatics pipeline (BING) for the analysis of NGS data that offers several novel computational approaches to 1. image alignment, 2. signal correlation, compensation, separation, and pixel-based cluster registration, 3. signal measurement and base calling, 4. quality control...
标签:
378. RECOUNT
Probabilistic tag count error correction for next generation sequencing data (Solexa/Illumina).
标签:RNA-Seq Quantitation
379. Gk arrays
Gk-arrays are a data structure to index the k-mers in a collection of reads.
标签:Genomics, Transcriptomics,Metagenomics
380. Tripal
Tripal is a collection of open-source, freely-available Drupal modules that serves as a web interface for a GMOD Chado database. It is designed to allow anyone with genomic data to quickly create an online genomic database using community supported tools. Tripal is part of the open-sour...
标签:Genomics, Genetics