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Annotation and Ranking of Structural Variation
Created
2019-07-09
254 commits to master branch, last one 3 months ago
🌲 An easy-to-use and scalable toolkit for genomic alteration signature (a.k.a. mutational signature) analysis and visualization in R https://shixiangwang.github.io/sigminer/reference/index.html
Created
2018-12-30
1,261 commits to master branch, last one 2 months ago
Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
Created
2021-01-26
188 commits to main branch, last one 5 months ago
cfDNApipe: A comprehensive quality control and analysis pipeline for cell-free DNA high-throughput sequencing data
Created
2021-01-11
769 commits to master branch, last one 2 years ago
ClassifyCNV: a tool for clinical annotation of copy-number variants
Created
2020-07-15
21 commits to master branch, last one about a year ago
Copy Number Variation
Created
2023-06-27
11 commits to main branch, last one about a year ago
Copy number variant caller and depth visualization utility for PacBio HiFi reads
Created
2022-04-06
21 commits to main branch, last one 2 months ago
Detection of allele-specific subclonal copy number alterations from single-cell transcriptomic data.
Created
2022-11-21
118 commits to master branch, last one 2 months ago