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dranew / packages

Package Name Access Summary Updated
shapeit4 public fast and accurate method for estimation of haplotypes (phasing) 2025-03-25
scicone public Single-cell copy number calling and event history reconstruction 2025-03-25
bioconductor-hmmcopy-single-cell public Corrects GC and mappability biases for readcounts (i.e. coverage) in non-overlapping windows of fixed length for single whole genome samples, yielding a rough estimate of copy number for furthur analysis. Designed for rapid correction of high coverage whole genome tumour and normal samples. 2025-03-25
destruct_utils public Bioinformatics tool for joint prediction of rearrangement breakpoints from single or multiple tumour samples 2025-03-25
cplex public CPLEX optimization studio 2025-03-25
bioconductor-aneufinder public This package implements functions for CNV calling, plotting, export and analysis from whole-genome single cell sequencing data. 2025-03-25
bioconductor-aneufinderdata public This package implements functions for CNV calling, plotting, export and analysis from whole-genome single cell sequencing data. 2025-03-25
r-cowplot public Some helpful extensions and modifications to the 'ggplot2' package. In particular, this package makes it easy to combine multiple 'ggplot2' plots into one and label them with letters, e.g. A, B, C, etc., as is often required for scientific publications. The package also provides a streamlined and clean theme that is used in the Wilke lab, hence the package name, which stands for Claus O. Wilke's plot package. 2025-03-25
r-reordercluster public Tools for performing the leaf reordering for the dendrogram that preserves the hierarchical clustering result and at the same time tries to group instances from the same class together. 2025-03-25
bioconductor-bamsignals public This package allows to efficiently obtain count vectors from indexed bam files. It counts the number of reads in given genomic ranges and it computes reads profiles and coverage profiles. It also handles paired-end data. 2025-03-25
single_cell_pipeline public Bioinformatics pipeline for single cell analysis 2025-03-25
samtools public Tools for dealing with SAM, BAM and CRAM files 2025-03-25
bcl2fastq public bcl2fastq Conversion Software both demultiplexes data and converts BCL files generated by Illumina sequencing systems to standard FASTQ file formats for downstream analysis. 2025-03-25
nuseq public No Summary 2025-03-25
perl-bio-db-hts public No Summary 2025-03-25
lichee public No Summary 2025-03-25
spruce public No Summary 2025-03-25
lemon public No Summary 2025-03-25
mapscape public No Summary 2025-03-25
phylowgs public No Summary 2025-03-25
r-ascat public No Summary 2025-03-25
pvacseq public No Summary 2025-03-25
swagger-spec-validator public No Summary 2025-03-25
strict-rfc3339 public No Summary 2025-03-25
connexion public No Summary 2025-03-25
clickclick public No Summary 2025-03-25
blossomv public Python wrapper for the Blossom V algorithm 2025-03-25
theta public Tumor Heterogeneity Analysis (THetA) is an algorithm that estimates the tumor purity and clonal/subclonal copy number aberrations directly from high-throughput DNA sequencing data. 2025-03-25
bnpy public Bayesian nonparametric machine learning for python. 2025-03-25
bicseq2-seg public No Summary 2025-03-25
bicseq2-norm public No Summary 2025-03-25
r-ada public Performs discrete, real, and gentle boost under both exponential and logistic loss on a given data set. The package ada provides a straightforward, well-documented, and broad boosting routine for classification, ideally suited for small to moderate-sized data sets. 2025-03-25
samblaster public A tool to mark duplicates and extract discordant and split reads from sam files. 2025-03-25
delly_utils public Structural variant discovery by integrated paired-end and split-read analysis 2025-03-25
remixt public ReMixT is a tool for joint inference of clone specific segment and breakpoint copy number in whole genome sequencing data 2025-03-25
biobambam2 public Tools for early stage alignment file processing 2025-03-25
libmaus2 public collection of data structures and algorithms 2025-03-25
libmaus public libmaus is a collection of data structures and algorithms 2025-03-25
boost_lib public Library for boost c++ 2025-03-25
citup public Clonality inference in multiple tumor samples using phylogeny 2025-03-25
shapeit public SHAPEIT is a fast and accurate method for estimation of haplotypes (aka phasing) from genotype or sequencing data. 2025-03-25
hmmcopy_utils public Utilities for HMMCopy 2025-03-25
gsl public No Summary 2025-03-25
clonehd public High-definition reconstruction of clonal composition from next-generation sequencing data 2025-03-25
bioconductor-titan public Corrects GC and mappability biases for readcounts (i.e. coverage) in non-overlapping windows of fixed length for single whole genome samples, yielding a rough estimate of copy number for furthur analysis. Designed for rapid correction of high coverage whole genome tumour and normal samples. 2025-03-25
r-argparse public A command line parser to be used with Rscript to write "#!" shebang scripts that gracefully accept positional and optional arguments and automatically generate usage. 2025-03-25
r-findpython public Package designed to find an acceptable python binary. 2025-03-25
bioconductor-hmmcopy public Corrects GC and mappability biases for readcounts (i.e. coverage) in non-overlapping windows of fixed length for single whole genome samples, yielding a rough estimate of copy number for furthur analysis. Designed for rapid correction of high coverage whole genome tumour and normal samples. 2025-03-25
defuse public Bioinformatics tool for gene fusion discovery using RNA-Seq data 2025-03-25
biowrappers public No Summary 2025-03-25

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