Stars
Efficient merging of structural variants from multiple SV callers and samples
Python tool for converting files and office documents to Markdown.
A short tandem repeat (STR) genotyping and analysis toolkit for long reads
A local-haplotagging-based small and structural variant caller
Generic targeted local assembler and genotyper for long-read data
tools for working with Bisulfite Sequencing data while preserving reads intrinsic dependencies
A tool for motif annotation and visualization in tandem repeats.
Fast and exact gap-affine partial order alignment
Tool for plotting sequencing data along genomic coordinates.
A program for the analysis of single cell nanopore long read data
SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel
A tool for somatic structural variant calling using long reads
Demultiplexing pooled scRNA-seq data with or without genotype reference
Efficient genotyping bi-allelic SNPs on single cells
Framework for sensitive DE testing (using neighbourhoods)
ClairS - a deep-learning method for long-read somatic small variant calling
Copy number caller for long read data including SNV utilization
π π π―π¨π₯π effortlessly translates differential expression datasets and RNAseq data into informative volcano plots. Highlight genes of interest with unprecedented ease. With just a single line of code,β¦