JosephLalli
MD/PhD Graduate Student at the University of Wisconsin-Madison. I enjoy thinking about how ACGTs change, and what those changes do.
Werling LabMadison, WI
JosephLalli's Stars
joshpxyne/gpt-migrate
Easily migrate your codebase from one framework or language to another.
mre/idiomatic-rust
🦀 A peer-reviewed collection of articles/talks/repos which teach concise, idiomatic Rust.
moshi4/pyCirclize
Circular visualization in Python (Circos Plot, Chord Diagram, Radar Chart)
owkin/PyDESeq2
A Python implementation of the DESeq2 pipeline for bulk RNA-seq DEA.
j-andrews7/awesome-bioinformatics-benchmarks
A curated and summarized list of bioinformatics bench-marking papers and resources.
jermp/data_compression_course
A Crash Course on Data Compression.
CompEpigen/figeno
Tool for plotting sequencing data along genomic coordinates.
lgmgeo/AnnotSV
Annotation and Ranking of Structural Variation
jmschrei/tangermeme
Biological sequence analysis for the modern age.
marschall-lab/panacus
Panacus is a tool for computing statistics for GFA-formatted pangenome graphs
stephenslab/mashr
An R package for multivariate adaptive shrinkage.
Illumina/PlatinumGenomes
The Platinum Genomes Truthset
TileDB-Inc/TileDB-Vector-Search
Cloud-native vector similarity search and storage with efficient, serverless scale-out
schatzlab/crossstitch
Code for phasing SVs with SNPs
lskatz/awesome-bioinformatics-jobs
Resources for bioinformatics jobs
at-cg/PanAligner
Long read aligner for cyclic and acyclic pangenome graphs
Midnighter/nextflow-gotchas
A collection of unexpected challenges and learnings with nextflow and nf-core.
asylvz/SVarp
Phased structural variant discovery in pangenomes
srbehera/DRAGEN_Analysis
piquelab/QuASAR
Quantitative Allele Specific Analysis of Reads. Joint genotyping & ASE inference for RNA-seq data
tkzeng/GeneBayes
COMBINE-lab/piscem
Rust wrapper for the next generation (still currently in C++)
fritzsedlazeck/nibSV
Kmer based genotyper for short reads.
gjun/muCNV
kcleal/SV_Benchmark_CMRG
Structural variant benchmark of challenging medically relevant genes
rwk-unil/sapphire
Smart and Accurate Polishing of Phased Haplotypes Integrating Read Enhancements (SAPPHIRE)
bw2/ExpansionHunter
A tool for estimating repeat sizes
ni-lab/CellTypeSpecificAccessibilityPrediction
courtrun/HLA_finngen
pengkenlim/LSTrAP-denovo
LSTrAP-denovo is an easy-to-use pipeline to assemble and annotate transcripts for species without genome / genomic annotations using publicly available RNA-seq data.