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  2. List of open-source bioinformatics software - Wikipedia

    en.wikipedia.org/wiki/List_of_open-source...

    Suite of packages for sequencing, searching, etc. written in C: Linux, macOS, Unix, Windows [4] GPL and LGPL: Collaborative project Galaxy: Scientific workflow and data integration system Unix-like: Academic Free: Collaborative project GenePattern: Scientific workflow system that provides access to hundreds of genomic analysis tools

  3. List of RNA-Seq bioinformatics tools - Wikipedia

    en.wikipedia.org/wiki/List_of_RNA-Seq...

    GenePattern is a freely available online platform that provides access to RNA-Seq analysis methods without the need for programming. GeneProf Freely accessible, easy to use analysis pipelines for RNA-seq and ChIP-seq experiments. GREIN is an interactive web platform for re-processing and re-analyzing GEO RNA-seq data. GREIN is powered by the ...

  4. Bowtie (sequence analysis) - Wikipedia

    en.wikipedia.org/wiki/Bowtie_(sequence_analysis)

    The Bowtie sequence aligner was originally developed by Ben Langmead et al. at the University of Maryland in 2009. [3] The aligner is typically used with short reads and a large reference genome, or for whole genome analysis. Bowtie is promoted as "an ultrafast, memory-efficient short aligner for short DNA sequences."

  5. List of sequence alignment software - Wikipedia

    en.wikipedia.org/wiki/List_of_sequence_alignment...

    REAL is an efficient, accurate, and sensitive tool for aligning short reads obtained from next-generation sequencing. The programme can handle an enormous amount of single-end reads generated by the next-generation Illumina/Solexa Genome Analyzer. cREAL is a simple extension of REAL for aligning short reads obtained from next-generation ...

  6. TopHat (bioinformatics) - Wikipedia

    en.wikipedia.org/wiki/TopHat_(bioinformatics)

    TopHat is an open-source bioinformatics tool for the throughput alignment of shotgun cDNA sequencing reads generated by transcriptomics technologies (e.g. RNA-Seq) using Bowtie first and then mapping to a reference genome to discover RNA splice sites de novo. [1] TopHat aligns RNA-Seq reads to mammalian-sized genomes. [2]

  7. ChIP sequencing - Wikipedia

    en.wikipedia.org/wiki/ChIP_sequencing

    ChIP-sequencing, also known as ChIP-seq, is a method used to analyze protein interactions with DNA. ChIP-seq combines chromatin immunoprecipitation (ChIP) with massively parallel DNA sequencing to identify the binding sites of DNA-associated proteins. It can be used to map global binding sites precisely for any protein of interest.

  8. Peak calling - Wikipedia

    en.wikipedia.org/wiki/Peak_calling

    It is also possible to do more complex analysis using such tools like combining multiple ChIP-seq signal to detect regulatory sites. [10] In the context of ChIP-exo, this process is known as 'peak-pair calling'. [11] Differential peak calling is about identifying significant differences in two ChIP-seq signals. One can distinguish between one ...

  9. Molecular Evolutionary Genetics Analysis - Wikipedia

    en.wikipedia.org/wiki/Molecular_Evolutionary...

    Alignment Editor ― Within MEGA, the Alignment Editor is a tool that may be used for editing and building multiple sequence alignments. The Alignment Editor in MEGA includes an integrated tool for both ClustalW and MUSCLE programs. All actions take place in the Analysis Explorer, which can be found in the main menu of MEGA.

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