Pinned Repositories
SCEVAN
R package that automatically classifies the cells in the scRNA data by segregating non-malignant cells of tumor microenviroment from the malignant cells. It also infers the copy number profile of malignant cells, identifies subclonal structures and analyses the specific and shared alterations of each subpopulation.
figeno
Tool for plotting sequencing data along genomic coordinates.
delly
DELLY2: Structural variant discovery by integrated paired-end and split-read analysis
SURVIVOR
Toolset for SV simulation, comparison and filtering
ClusterGVis
One-step to Cluster and Visualize Gene Expression Matrix
Severus
A tool for somatic structural variant calling using long reads
minimap2
A versatile pairwise aligner for genomic and spliced nucleotide sequences
Ribbon
A genome browser designed for complex structural variants and long reads.
copykat
whatshap
Read-based phasing of genomic variants, also called haplotype assembly
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