GENE-counter is a complete Perl-based computational pipeline for analyzing RNA-Sequencing (RNA-Seq) data for differential gene expression. In addition to its use in studying transcriptomes of eukaryotic model organisms, GENE-counter is applicable for prokaryotes and non-model organisms without an available genome reference sequence. For alignments, GENE-counter is configured for CASHX, Bowtie, and BWA, but an end user can use any Sequence Alignment/Map (SAM)-compliant program of preference.

Cumbie JS, Kimbrel JA, Di Y, Schafer DW, Wilhelm LJ, Fox SE, Sullivan CM, Curzon AD, Carrington JC, Mockler TC, Chang JH. (2011) GENE-Counter: A Computational Pipeline for the Analysis of RNA-Seq Data for Gene Expression Differences. PLoS One 6(10), e25279. [article]

 

S-MART is a toolbox which handles mapped RNA-Seq data. S-MART is an intuitive and lightweight tool which performs many of the tasks usually required for the analysis of mapped RNA-Seq reads. S-MART does not require any computer science background and thus can be used by all of the biologist community through a graphical interface. S-MART can run on any personal computer, yielding results within an hour even for Gb of data for most queries. S-MART may perform the entire analysis of the mapped reads, without any need for other ad hoc scripts. With this tool, biologists can easily perform most of the analyses on their computer for their RNA-Seq data, from the mapped data to the discovery of important loci.

S-MART can be downloaded for free from http://urgi.versailles.inra.fr/Tools/S-MART, and can be used on any platform (Linux, Windows or Mac). S-MART has been developed under the CeCILL license, which is compatible with the GNU GPL license.

  • Zytnicki M, Quesneville H. (2011) S-MART, A Software Toolbox to Aid RNA-seq Data Analysis. PLoS One. 6(10), e25988. [article]

Incoming search terms:

  • rna sequencing data analysis software
  • rna-seq analysis tool
  • rna seq genetic network software
  • rnaseq differential analysis software
  • rna-seq expression windows pc software
  • * seq analysis software
  • rna sequencing analysis software windows
  • RNA seq soft ware
  • rna seq expression software
  • rna seq data analysis windows

Comments

Leave a Reply




  • Social Networking Pages

    Linkedin Group

  • Follow Me on Pinterest
  • RSS SEQanswers – RNA Sequencing

    • How to increase rowsize in heatmap? May 16, 2013
      Hi, I am a complete newbie to all things cummeRbund and am currently fighting with generating readable heatmaps. When I use ... […]
      Mags
    • novoalign mapping May 15, 2013
      Hi, I want to use novoalign to map reads - allowing up to 15 mismatches for 100 bp paired-end reads I am new to novoalign(went through the... […]
      abh
    • Design of expt across multiple lanes May 15, 2013
      Hi, I am performing an RNA-seq experiment to look at differential expression. The design is as follows: 2 populations x 3 biological... […]
      jbono
    • RNA kinds expected in RNA-seq results May 15, 2013
      Hi, We use RNA isolation and library preparation protocols which capture polyadenylated RNA. My question is what kinds of RNA can we expect to... […]
      Kocur
    • Discrepancy between genotype and expressed alleles May 15, 2013
      Hi all, I am working on the analysis of allele-specific expression using both genotype information and RNA-seq data from the same individuals. I... […]
      RedMary
    • Does Cufflinks Give Me Trascriptomes? May 14, 2013
      Hi Everyone, I'm a beginner in this area, please forget any silly question. My situation is that I have a raw scaffold whole genome... […]
      hchang10
  • RSS Biostar – RNA-Seq

    • How do TopHat options -g , --supress-hits, and Bowtie options interplay?
      Hi, I am currently using TopHat2 to map RNA-seq runs. I think there have been some changes pertaining the -g option. Does anyone know how it works now? I used to think that setting -g would look for n alignments for a given read, report them [if top-scoring] and discard those reads that had more than g [top scoring] alignments. Now, the description sounds mo […]
    • What happened to -k in TopHat for multiple-mapping reads?
      Selecting -g n in tophat does not discard reads mapping more than n, but instead only reports n alignments for those out all all their TOP scoring alignments. I think there used to be an option -k that would allow one to discard reads that topped x alignments -- whatever happened to that? I only see -g in the tophat 2 manual, no reporting options like before […]
    • Does tophat use the library-type information for mapping, or just for the XS flag?
      When I specify library-type to TopHat, i.e., first-strand, second-strand, unstranded, TopHat appends a value + or - to the XS:A tag, which is useful for subsequent analyses, such as annotation. However, does this information influence the "mappability" of reads, or is this unaffected? My guess is that the information will be considered for mapping […]
    • Purpose of Y-shaped adapters in Illumina Sequencing?
      Hi all, Y adapters different sequences to be annealed to the 5' and 3' ends of each molecule in a library. The arms of the Y are unique, and the middle part, connected to the DNA fragment, is complementary. What are the advantages of this? My take of this over having fully-complementary adapters (ADAPTER1 - - - - - ADAPTER1) is that: -Upon primer a […]
    • Cell Type composition in a tissue based on gene marker expression
      I am not sure if the following would even make sense.... Tissues are composed of composite cell types, and often there are studies such as microarray/NGS where we perform a collective sampling of cells from these tissues. Information about the composition (say percentage of cell type) is not taken into consideration. In some case (such as brain/cancer), ther […]
    • Which SNP caller / method to use after aligning RNA-seq with TopHat
      Which SNP caller / method can / should I use after aligning RNA-seq data with TopHat? For genomic data I use GATK, but supposedly it is not just as easy as running GATK on the TopHat RNA-seq data. The team from Broad has no information / documentation on how to use GATK for RNA-seq data. I don't have any variants yet from DNA re-sequencing. […]