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Various algorithms for analysing genomics data

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HMF Tools

This repository contains the suite of tools used in the Hartwig Medical Foundation whole genome,targeted DNA and whole transcriptome analysis pipeline.

DNA Pipeline Components

HMF_Pipeline

The table below has links for the full functional detail and configuration for each component. The versions match those used in the current HMF GCP pipeline which can be run using Platinum.

Current versions

Component Description Current Version
Amber Generate a tumor BAF file for Purple's copy number fit 3.9
Cobalt Determines the read depth ratios for Purple's copy number fit 1.13
Cuppa Tissue of origin prediction from WGS/WTS 1.6
Gripss SV filtering 2.2
Lilac HLA typing 1.2
Linx SV annotation, clustering & chaining, fusion and disruption calling 1.20
Pave Point mutation annotation and gene impact 1.3
Purple Estimates copy number, purity and ploidy, and identifies driver events 3.5
Sage Point mutation variant calling and filtering 3.1
Teal Measures telomere content and estimates telomeric length 1.0.1

The following external tools are used in the pipeline:

Component Description Current Version
GRIDSS Structural variant calling 2.13.2
Chord Homologous Recombination Deficiency detection 2.0

Demo pipeline

A example pipeline which runs each of these components in turn is detailed here.

Resource files

Resource files for each component (GRCh37 and GRCh38) are available to download from HMFTools-Resources > DNA-Resources.

Actionability and Clinical Reporting Tools

Component Description Current Version
Serve Harmonisation of evidence from clinical annotation databases 1.12
Protect Matching of molecular results to treatments and clinical trials 2.3
Rose Actionability of clinically relevant molecular findings 1.1
Virus Interpreter Filtering, annotation and interpretation of virus breakend data 1.2
Orange PDF summary report and JSON file of all WGS output 1.10
Patient-reporter PDF summary report and JSON file of all clinical relevant WGS output 7.25.1

RNA Tools

Component Description Current Version
Isofox WTS Transcript Abundance, Fusions & Novel Splice Junctions 1.5

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Various algorithms for analysing genomics data

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