JosephLalli/gbwt
Substring index for paths in a graph
MD/PhD student at UWisc-Madison. I enjoy thinking about how ACGTs change, and what those changes do. Currently applying to Psychiatric residency programs.
Substring index for paths in a graph
xg0: a simpler xg index
Optimized sequence graph implementations for graph genomics
tools for working with genome variation graphs
BWT-based index for graphs
Versioned methods for the BrainVar GRCh38 and T2T counterfactual reproduction
Segmented HAPlotype Estimation and Imputation Tool
Repository for code to produce phased 1000 Genomes Project haplotypes called against the CHM13v2 T2T reference genome.
Tool to liftover variants between references in an indel-aware manner
Ultrafast GPU-based QTL mapper
Reproducible BrainVar2 GRCh38 whole-genome germline variant-calling workflow
Portable BrainVar and BrainVar2 QTLtools MBV sample-matching workflow and decision documentation
Python wrapper for wavefront alignment using WFA2-lib
vcfdist: Accurately benchmarking phased variant calls
Codex-native multi-agent development environment scaffold for multiSHAPE
multiSHAPE is an extension of SHAPEIT4/5 to simultaneous biallelic and multiallelic genotype phasing.
ATAC-seq peak-calling and QC analysis pipeline
A new model and algorithm for multivariate Bayesian variable selection regression.
Segmented HAPlotype Estimation and Imputation Tool
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Archived copy of old sarek fork
Tool to calculate allelic bias in aligned, variant called sequencing datasets
Pipelines to create and analyze ENCODE candidate cis-Regulatory Elements
Scripts and utilities for analyzing tandem repeats (TRs).
Tool to calculate nucleotide diversity statistics in large pooled population datasets