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HTSeq: Analysing high-throughput sequencing data with Python

  • Overview
    • Documentation overview
    • Author
    • License
  • Prequisites and installation
    • Prequisites
    • Download
    • Installing a binary package
    • Installing a source package
  • A tour through HTSeq
    • Reading in reads
    • Genomic intervals and genomic arrays
    • Calculating coverage vectors
    • Counting reads by genes
    • Mapping structural variants to genes
    • And much more
  • A detailed use case: TSS plots
    • Using the full coverage
    • Using indexed BAM files
    • Streaming through all reads
  • Sequences and FASTA/FASTQ files
    • Sequence
    • SequenceWithQualities
    • FastaReader
    • FastqReader
  • Genomic intervals and genomic arrays
    • GenomicInterval
    • GenomicPosition
    • GenomicArray
    • GenomicArrayOfSets
  • Read alignments
    • Concepts
    • Parser classes
    • Alignment and AlignmentWithSequenceReversal
    • Format-specific Alignment classes
    • Multiple alignments
    • CIGAR strings
  • Features
    • GFF_Reader and GenomicFeature
    • VCF_Reader and VariantCall
  • Miscellaneous
    • FileOrSequence
    • Version
  • Quality Assessment with htseq-qa
    • Plot
    • Usage
  • Counting reads in features with htseq-count
    • Usage
  • Version history
    • Version 0.5.3
    • Version 0.5.2
    • Version 0.5.1
    • Version 0.5.0
    • Version 0.4.7
    • Version 0.4.6
    • Version 0.4.5
    • Version 0.4.4
    • Version 0.4.3
    • Version 0.4.2
    • Version 0.4.1
    • Version 0.4.0
    • Version 0.3.7
  • Notes for Contributers
    • Source code
    • Languages
    • Build process
    • Distributing
    • Files
  • Index

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