Get FastQ reads from the FastQ streamer
● Data Source:
BioConductor
● Keywords: internal
● Alias: FastQStreamer.getReads
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FastQStreamer.init
(Package: HTSeqGenie) :
Open a streaming connection to a FastQ file
Open a streaming connection to a FastQ file
● Data Source:
BioConductor
● Keywords: internal
● Alias: FastQStreamer.init
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Close the FastQStreamer
● Data Source:
BioConductor
● Keywords: internal
● Alias: FastQStreamer.release
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The HTSeqGenie package is a robust and efficient software to analyze high-throughput sequencing experiments in a reproducible manner. It supports the RNA-Seq and Exome-Seq protocols and provides: quality control reporting (using the ShortRead package), detection of adapter contamination, read alignment versus a reference genome (using the gmapR package), counting reads in genomic regions (using the GenomicRanges package), and read-depth coverage computation.
● Data Source:
BioConductor
● Keywords: package
● Alias: HTSeqGenie
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Build the genomic features of the TP53 demo region
● Data Source:
BioConductor
● Keywords:
● Alias: TP53GenomicFeatures
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alignReads
(Package: HTSeqGenie) :
Align reads against genome
Align reads against genome
● Data Source:
BioConductor
● Keywords: internal
● Alias: alignReads
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Genomic alignment using gsnap.
● Data Source:
BioConductor
● Keywords: internal
● Alias: alignReadsChunk
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Calculate and process Variants
● Data Source:
BioConductor
● Keywords:
● Alias: analyzeVariants
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Uniquely count number of reads in bam file
● Data Source:
BioConductor
● Keywords: internal
● Alias: bamCountUniqueReads
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buildConfig
(Package: HTSeqGenie) :
Build a configuration file based on a list of parameters
Build a configuration file based on a list of parameters
● Data Source:
BioConductor
● Keywords: internal
● Alias: buildConfig
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