Group: Renjin Bioconductor

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S4 generic functions needed by many Bioconductor packages.

Provides user interface and database connection code for annotation data packages using SQLite data storage.

A library of core preprocessing routines.

Provides efficient low-level and highly reusable S4 classes for storing, manipulating and aggregating over annotated ranges of integers. Implements an algebra of range operations, including efficient algorithms for finding overlaps and nearest ...

The ability to efficiently represent and manipulate genomic annotations and alignments is playing a central role when it comes to analyzing high-throughput sequencing data (a.k.a. NGS data).

A package that implements some simple graph handling capabilities.

The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions.

The SummarizedExperiment container contains one or more assays, each represented by a matrix-like object of numeric or other mode. The rows typically represent genomic ranges of interest and the columns represent samples.

Memory efficient string containers, string matching algorithms, and other utilities, for fast manipulation of large biological sequences or sets of sequences.

Define coerce methods for microarray data objects.

Using R enviroments for annotation.

Some basic functions for filtering genes

Many functions for computing the NPMLE for censored and truncated data.

This package provides modified versions and novel implementation of functions for parallel evaluation, tailored to use with Bioconductor objects.

This package provides an interface to the 'samtools', 'bcftools', and 'tabix' utilities (see 'LICENCE') for manipulating SAM (Sequence Alignment / Map), FASTA, binary variant call (BCF) and compressed indexed tab-delimited (tabix) files.

Non-parametric bootstrap and permutation resampling-based multiple testing procedures (including empirical Bayes methods) for controlling the family-wise error rate (FWER), generalized family-wise error rate (gFWER), tail probability of the ...

Genome wide annotation for Human, primarily based on mapping using Entrez Gene identifiers.

A set of annotation maps describing the entire Gene Ontology assembled using data from GO

Functions that are needed by many other packages or which replace R functions.

This package takes a list of p-values resulting from the simultaneous testing of many hypotheses and estimates their q-values and local FDR values. The q-value of a test measures the proportion of false positives incurred (called the false discovery ...