maegsul
Postdoctoral researcher at @SleegersLab-VIBCMN working on complex genetics of Alzheimer's. | GWAS, molecular QTLs, TWAS, splicing, long reads, rare variants.
Antwerp
maegsul's Stars
jokergoo/ComplexHeatmap
Make Complex Heatmaps
skovaka/UNCALLED
Raw nanopore signal mapper that enables real-time targeted sequencing
lgmgeo/AnnotSV
Annotation and Ranking of Structural Variation
broadinstitute/ABC-Enhancer-Gene-Prediction
Cell type specific enhancer-gene predictions using ABC model (Fulco, Nasser et al, Nature Genetics 2019)
pjedge/longshot
diploid SNV caller for error-prone reads
LooseLab/readfish
CLI tool for flexible and fast adaptive sampling on ONT sequencers
stephenturner/annotables
R data package for annotating/converting Gene IDs
odelaneau/GLIMPSE
Low Coverage Calling of Genotypes
ncbi/dbsnp
dbSNP
GoekeLab/sg-nex-data
Nanopore RNA-Seq data from the Singapore Nanopore-Expression Project
ChristopherWilks/megadepth
BigWig and BAM utilities
FinucaneLab/pops
tkzeng/Pangolin
Pangolin is a deep-learning method for predicting splice site strengths.
xqwen/fastenloc
Colocalization analysis of genetic association signals
eQTL-Catalogue/eQTL-Catalogue-resources
gagneurlab/MMSplice_MTSplice
Tissue-specific variant effect predictions on splicing
mehrdadbakhtiari/adVNTR
A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data
LappalainenLab/lorals
thewonlab/H-MAGMA
shimlab/NanoSplicer
xqwen/integrative
Software Pipeline for Integrative Genetic Association Analysis: Probabilistic Assessment of Enrichment and Colocalization
mancusolab/ma-focus
MA-FOCUS: Multi-Ancestry Fine-mapping Of CaUsal gene Sets
theodorc/Atlas-CNV
Method to detect exonic CNVs in NGS Gene Targeted Panels
collaborativebioinformatics/STRdust
bhattacharya-a-bt/MOSTWAS
Multi-Omic Strategies for TWAS
jackhump/leafviz
Just the leafviz parts of Leafcutter
hakyimlab/brainxcan
mortazavilab/swan_paper
Repository for commands used for the Swan manuscript
aneumann-science/omicsR2
aneumann-science/rare_variants_csf_biomarkers