MultiRepMacsChIPSeq - Applications
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Application documentation
Documentation for the applications included in this package.
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An application for removing duplicate alignments in a bam file. Unlike other applications, this can sub-sample and remove a random subset of alignments to reach an acceptable fraction of duplication.
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A simple application to combine the count data of replicates into single sample counts. It works with a tab-delimited text count table file.
-
An application to combine multiple metric values from Novocraft Novoalign output, bam_partial_dedup duplication statistics, bam2wig shift determination, and Macs2
predictd
shift determination. -
An application to generate a differential track (bedGraph or bigWig format) from two track files.
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An application to generate chromosomal mean coverage bedGraph from fragment coverage track file.
-
An application to properly intersect two or more peak files and generate a merged peak file along with multiple general statistics.
-
The main MultiRepMacsChIPSeq pipeline application.
-
An application to convert a
narrowPeak
file to a simplebed
file. -
An R script to generate multiple plot figures from data files generated by the MultiRepMacsChIPSeq pipeline.
-
An R script to generate a shift model plot from bam2wig shift determination files.
-
A simple application to generate a chromosome size file from an indexed track file, such as
bam
orbigWig
. -
An application for recalling peaks with different thresholds without having to re-run the entire MultiRepMacsChIPSeq pipeline.
-
An application to render a Markdown report into a self-contained HTML file using
pandoc
, providing reasonable if minimal styling. -
An application to report the fraction of a genome that is covered by unique and non-unique alignments from one or more bam alignment files.
-
A simple R script to run
DESeq2
on collected peak counts, particularly for differential peak analysis. -
An application to sort a data table by extrinsic keys, in this case by the samples that contributed to a peak call.
-
A convenience utility application to subset one or more bigWig tracks to a single chromosome, ostensibly to download to a personal computer for evaluation in a genome browser.
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An application to replace or update missing values in a
narrowPeak
format peak file using available track files.
Pertinent Bio::ToolBox Applications
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An application for generating coverage tracks from bam alignment files in nearly every possible way imaginable.
-
An application for generating
wig
,bedGraph
, andbigWig
files from a tab-delimited text file. -
An application for collecting data from track files over genomic features in a variety of methods.
-
An application for collecting data from track files in windows flanking a reference point.
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An interactive command-line application for working with tab-delimited text data files. Faster and easier than importing into Excel to do simple row- and column-based manipulations.
-
An application for performing manipulations on
wig
,bedGraph
, andbigWig
file formats.