Results for "detect"

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  • MOSS: A System for Detecting Software Similarity

    Moss (for a Measure Of Software Similarity) is an automatic system for determining the similarity of programs. To date, the main application of Moss has been in detecting plagiarism in programming classes. Since its development in 1994, Moss has been very effective in this role. The algorithm beh...

    Tags: MOSS, System, Detecting, Software, Similarity, detect, plagiarism, programming

    2324 days ago

  • Bioinformatics tools to detect horizontal gene transfer (HGT) in genomes

    Horizontal gene transfer (HGT), the “non-sexual movement of genetic material between two organisms” , is relatively common in prokaryotes and single-celled eukaryotes, but a number of factors combine to make it far rarer in multicellular eukaryotes. In order for a eukaryotic spec...

    Tags: Tools, detect, horizontal, gene, transfer, HGT, genomes

    835 days ago

  • EXCAVATOR: detecting copy number variants from whole-exome sequencing data

    EXCAVATOR, for the detection of copy number variants (CNVs) from whole-exome sequencing data. EXCAVATOR combines a three-step normalization procedure with a novel heterogeneous hidden Markov model algorithm and a calling method that classifies genomic regions into five copy number states. We vali...

    Tags: EXCAVATOR, detect, copy, number, variants, whole-exome, sequencing, data

    1933 days ago

  • CroCo: A program to detect potential cross contaminations in HTS assembled transcriptomes using expression level quantification

    CroCo is a program to detect cross contamination events in assembled transcriptomes using sequencing reads to determine the true origin of every transcripts.Such cross contaminations can be expected if several RNA-Seq experiments were prepared during the same period at the same lab, or by the sam...

    Tags: CroCo, program, detect, potential, cross, contaminations, HTS, assembled, transcriptomes, expression, quantification

    1930 days ago

  • ClipCrop: a tool for detecting structural variations with single-base resolution using soft-clipping information

    ClipCrop for detecting SVs with single-base resolution using soft-clipping information. A soft-clipped sequence is an unmatched fragment in a partially mapped read. To assess the performance of ClipCrop with other SV-detecting tools, we generated various patterns of simulation data – SV len...

    Tags: ClipCrop, tool, detect, structural, variations, single-base, resolution, soft-clipping, information

    1917 days ago

  • MAJIQ 2 is released !

      Ability to detect, quantify, and visualize complex and de-novo splicing variations from RNASeq. MAJIQ’s accuracy compares favorably to other algorithms. MAJIQ 2 is *way* faster, more memory and I/O efficient New visualization (VOILA 2.0) Ability to analyze hundreds and thousands ...

    Tags: Majiq, Voila, detect, quantify, visualize, complex, de-novo, splicing, variations, RNASeq

    1381 days ago

  • fastv - detect virus

    fastv is an ultra-fast tool for identification of SARS-CoV-2 and other microbes from sequencing data. It detects microbial sequences from FASTQ data, generates JSON reports and visualizes the result in HTML reports. This tool can be used to detect viral infectious diseases, like COVID-19. This to...

    Tags: virus, detect, fast, identification

    861 days ago

  • chromeister: An ultra fast, heuristic approach to detect conserved signals in extremely large pairwise genome comparisons.

    chromeister: An ultra fast, heuristic approach to detect conserved signals in extremely large pairwise genome comparisons. USAGE: -query: sequence A in fasta format -db: sequence B in fasta format -out: output matrix -kmer Integer: k>1 (default 32) Use 32 for chromosomes and genomes and...

    Tags: chromeister, fast, heuristic, approach, detect, conserved, signals, extremely, large, pairwise, genome, comparisons

    807 days ago

  • MUM&Co is a simple bash script that uses Whole Genome Alignment information provided by MUMmer (v4) to detect variants.

    MUM&Co is able to detect:Deletions, insertions, tandem duplications and tandem contractions (>=50bp & <=150kb)Inversions (>=1kb) and translocations (>=10kb)

    Tags: MUM&Co, simple, bash, script, Whole, Genome, Alignment, information, MUMmer, detect, variants

    724 days ago