wtsi-hpag

wtsi-hpag

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Software tools and pipelines developed by the High Performance Algorithms Group @ the Wellcome Sanger Institute

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wtsi-hpag's repositories

scanPAV

Pipeline to detect PAVs (presence/absence variations) in genome comparison using whole genome alignment.

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Scaff10X

Pipeline for scaffolding and breaking a genome assembly using 10x genomics linked-reads

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scaffHiC

Pipeline for genome scaffolding by modelling distributions of HiC pairs

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caus

CAUS is a pipeline for Chromosome Assignment Using Synteny

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easyChain

easyChain is a pipeline to produce a chain file from two genome assemblies.

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HiLine

HiC alignment and classification pipeline

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smis

SMIS: Single Molecular Integrative Scaffolding. A pipeline for scaffolding genome assemblies using long reads (PacBio, ONT)

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SamHaplotag

Process haplotag barcodes in SAM format

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AncesBin

Pipeline to bin 10X, HiC, PacBio and ONT reads based on ancestry assemblies

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SIMDExtensionWrapper

Generic wrapper program, detects SIMD CPU extensions and launches an appropriate sub-process.

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covidPileup

Pipeline for building SNP and GAP pileup from multiple COVID-19 whole genome sequences.

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scaffhtag

Pipeline for scaffolding genome assemblies using haplotagging reads

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chromoSPA

A Size and Positional Analysis (SPA) tool for studying chromothripsis breakages.

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ContactPointAnalysis

A statistical tool for analysing the Contact Point hypothesis for Chromothripsis

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CoverageWorkshop

A Workshop Notebook used for running a session as part of the OpenLab series.

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GenCHORD

A Bayesian method to smooth-out the noise in a coverage dataset, revealing the underlying average behaviour which is constrained to lie on `Harmonics' of a fundamental coverage value.

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HypoCoverage

Coverage Analysis Tools

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HypothesisTester

A Bayesian Statistical Inference framework for comparing hypotheses

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LinkStats

Collect and process statistics from aligned linked-reads.

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MCSampler

An MCMC Sampling framework for sampling from arbitrary probability densities.

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stepStone

A pipeline for identification of chromothripsis breakpoints and cancer rearrangements

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varibase

A pipeline to correct variation errors of SNPs/indles from genome assembly

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