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HTSeq 0.5.3p9 documentation
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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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HTSeq 0.5.3p9 documentation
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