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Showing 10 of 51 repositories
- parklab.github.io Public
- NanoSeq_parkLab Public Forked from cancerit/NanoSeq
Analysis software for Nanorate Sequencing (NanoSeq) experiments -- forked over from Sanger Institute
- EchoSV Public
A novel tool for accurately merging haplotype-based SV calls and comparing SVs across reference genomes
- zhou_luquette_2026_genomic_damage_in_neurodegeneration Public
Scripts to recreate analyses in Zhou, Luquette et al. Cell 2026.
- reference_genomes_decoy_analysis Public
Scripts to analyze read alignment and variant calling from simulated and empirical data based on different human reference genome versions.
- xTea Public
Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics
- Illumina-TwoColorBias Public
A repository containing code to correct T>N mutation bias in NovaSeq 6000 callsets
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