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@Bioinformatics-pipelines

Bioinformatics-pipelines

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  1. bamToFreq bamToFreq Public

    Forked from matdoering/bamToFreq

    Converts mapped next-generation sequencing reads in BAM format to the tabular frequency file format that is used by geno2pheno[ngs-freq]

    Shell

  2. fastqToFreq fastqToFreq Public

    Forked from matdoering/fastqToFreq

    Uses MinVar and bamToFreq to transform NGS reads (FASTQ) to frequency files (CSV)

    Python

  3. MinVar MinVar Public

    Forked from medvir/MinVar

    A tool to detect minority variants in HIV-1 and HCV populations

    Python

  4. variant-calling variant-calling Public

    Forked from medvir/variant-calling

    computes all variants including indels from Illumina sequences compared to a reference sequence

    Python

  5. mutationalProfiles mutationalProfiles Public

    Forked from cclab-brca/mutationalProfiles

    R

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