nhansen

AlphaThal

Pipeline for retrieving reads from the Alpha Thalassemia region

bam2mpg

Software for calling variants from next-generation sequence data.

BardCNV

BardCNV calls copy number variants from next generation sequencing data.

mlgenofeatures

mlgenotype

Python package for training and using machine learning models to recognize structural variants using features of aligned short read data

MMBVariantCalling

Scripts and updates for running the variant pipeline described in "Variant Calling From Next Generation Sequence Data" by Nancy F. Hansen

NovoGraph

NovoGraph: building whole genome graphs from long-read-based de novo assemblies

q100bench

Software for comparing genome assemblies and read datasets to a benchmark genome like the Q100 project's HG002v1.0.1

Shimmer

Shimmer is a software package for the characterization of genetic differences between two very similar samples, e.g., a tumor sample and its matched normal tissue sample.

SVanalyzer

Tools for the analysis of structural variation in genomes

nhansen/SVanalyzer

Tools for the analysis of structural variation in genomes

nhansen/Shimmer

Shimmer is a software package for the characterization of genetic differences between two very similar samples, e.g., a tumor sample and its matched normal tissue sample.

nhansen/bam2mpg

Software for calling variants from next-generation sequence data.

nhansen/MMBVariantCalling

Scripts and updates for running the variant pipeline described in "Variant Calling From Next Generation Sequence Data" by Nancy F. Hansen

nhansen/q100bench

Software for comparing genome assemblies and read datasets to a benchmark genome like the Q100 project's HG002v1.0.1

nhansen/NovoGraph

NovoGraph: building whole genome graphs from long-read-based de novo assemblies

nhansen/BardCNV

BardCNV calls copy number variants from next generation sequencing data.

nhansen/mlgenofeatures

nhansen/mlgenotype

Python package for training and using machine learning models to recognize structural variants using features of aligned short read data

nhansen/AlphaThal

Pipeline for retrieving reads from the Alpha Thalassemia region

nhansen/bioconda-recipes

Conda recipes for the bioconda channel.

nhansen/issue-dump

Place to send issues created in error

nhansen/issue-playground

Testing repository for issue templates and trigger to google sheet

nhansen/LateStageEECs

Statistical analysis software used in Rudd et al., "KLF3 and PAX6 are candidate driver genes in late-stage, MSI-hypermutated endometrioid 2 endometrial carcinomas"

nhansen/github_issues

Python software to create and retrieve GitHub issues and write spreadsheets to Google Sheets with issue metadata

nhansen/nhansen

nhansen/nhansen.github.io

Documentation for Nancy Hansen's software tools

nhansen/NHGRI-BW2

Software to automate tasks for performing biowulf2 analyses remotely from a different server.

nhansen/RFGenotypeManuscript2023

Scripts and data files for "Random forest classifiers trained on simulated data enable accurate short read-based genotyping of structural variants in the alpha thalassemia genomic region"

nhansen/SleepInbredPanel

nhansen/T2Tvariants

Code used for Aganezov et al., A complete reference genome improves analysis of human genetic variation. bioRxiv, 2021.