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  • RNA CoMPASS v1.0 released!

    RNA CoMPASS, a web-based GUI distributed computational pipeline, provides all-in-one functionality including human transcriptome quantification and the typical endogenous RNA-Sequencing analysis along with the investigation of exogenous sequences. RNA CoMPASS is deployable on either a local cluster or a grid environment managed by PBS submission.

    The key features include,
    Discovery and visualization of exogenous sequences of non-host origin
    * Aligns short RNA sequences against human, virus and bacterial genomes
    * Searches unmapped sequences against human RNA and NT databases
    * Visualizes taxonomic distribution of reads using MEGAN
    * Assembles pools of exogenous reads into longer transcripts with ABySS
    (Currently under development)

    Performs extensive endogenous RNA-Seq analysis for the host organism
    * Calculates genomic feature abundance score at both gene and isoform level
    * Detects differentially expressed genes and isoforms with support for edgeR
    * Generates wiggle files for visualization and signal maps for peak detection
    * Generates alignment report summarizing distribution of read mappings

    The software is available for download at:

Latest Articles

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  • seqadmin
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    Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
    12-16-2024, 07:57 AM
  • seqadmin
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    Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

    Long-Read Sequencing
    Long-read sequencing has seen remarkable advancements,...
    12-02-2024, 01:49 PM

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