|
vcf2maf_shahcompbio
|
public |
vcf2maf conversion
|
2025-03-25 |
|
wgs_qc_html
|
public |
No Summary
|
2025-03-25 |
|
single_cell_pipeline_hmmcopy_emilia
|
public |
Bioinformatics pipeline for single cell analysis
|
2025-03-25 |
|
oncokb-annotator
|
public |
No Summary
|
2025-03-25 |
|
pypdf2
|
public |
pdf toolkit for python
|
2025-03-25 |
|
single_cell_pseudo_bulk_qc
|
public |
No Summary
|
2025-03-25 |
|
pseudo_bulk_qc_html_report
|
public |
No Summary
|
2025-03-25 |
|
cell_cycle_classifier
|
public |
Cell cycle classifier for DLP+ data.
|
2025-03-25 |
|
single_cell_pipeline_annotation
|
public |
Bioinformatics pipeline for single cell analysis
|
2025-03-25 |
|
single_cell_pipeline_hmmcopy
|
public |
Bioinformatics pipeline for single cell analysis
|
2025-03-25 |
|
destruct_utils
|
public |
Utility scripts for destruct.
|
2025-03-25 |
|
circos_utils
|
public |
Utility scripts for circos plotting.
|
2025-03-25 |
|
titan_wgs_utils
|
public |
Utility scripts for titan.
|
2025-03-25 |
|
titan_wgs
|
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 |
|
single_cell_pipeline_align
|
public |
Bioinformatics pipeline for single cell analysis
|
2025-03-25 |
|
lumpy-sv
|
public |
A general probabilistic framework for structural variant discovery
|
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 |
|
corrupt-tree
|
public |
tree for single cell dna
|
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 |
|
museqportrait
|
public |
No Summary
|
2025-03-25 |
|
biowrappers
|
public |
No Summary
|
2025-03-25 |
|
museq
|
public |
Software for somatic SNV detection using next generation sequencing (NGS) data.
|
2025-03-25 |
|
pypeliner
|
public |
Library for creating informatic workflows
|
2025-03-25 |
