Joseph Lalli's Projects
Bonito - A PyTorch Basecaller for Oxford Nanopore Reads
Differential transcript and gene expression, as well as helper functions for working with Salmon, alevin, and alevin-fry data
Personal diploid genome creation and coordinate conversion
Annotation-free quantification of RNA splicing. Yang I. Li, David A. Knowles, Jack Humphrey, Alvaro N. Barbeira, Scott P. Dickinson, Hae Kyung Im, Jonathan K. Pritchard
Repository to host tool-specific module files for the Nextflow DSL2 community!
A DSL for data-driven computational pipelines
Incorporating pre/post variant filtering when aligning to reference pangenomes
Repository for code to produce phased 1000 Genomes Project haplotypes called against the CHM13v2 T2T reference genome.
Tool to calculate nucleotide diversity statistics in large pooled population datasets
Portable eQTL analysis and statistical fine mapping workflow used by the eQTL Catalogue
RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control. Includes ngscheckmate.
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
add statistical annotations (pvalue significance) on an existing boxplot generated by seaborn boxplot
add statistical annotations (pvalue significance) on existing boxplot/barplot generated by seaborn
Training models for basecalling Oxford Nanopore reads
Ultrafast GPU-based QTL mapper