JiaqiLiZju / NvwaView external linksLinks
☆36Sep 25, 2022Updated 3 years ago
Alternatives and similar repositories for Nvwa
Users that are interested in Nvwa are comparing it to the libraries listed below
Sorting:
- ☆15May 22, 2025Updated 8 months ago
- Code used in article: Tracing cell-type evolution by cross-species comparison of cell atlases☆18Aug 11, 2020Updated 5 years ago
- BPNet manuscript code.☆12Dec 1, 2020Updated 5 years ago
- iFISH Probe Design: a Python3 package to build iFISH probes.☆12Mar 11, 2022Updated 3 years ago
- Learning motif contributions to cell transitions using sequence features and graphs.☆28Aug 30, 2024Updated last year
- Combine structural variation outputs from long sequencing reads into a superior call set☆18Aug 6, 2025Updated 6 months ago
- ☆48Jan 7, 2025Updated last year
- Methods and analysis for Garcia-Nieto, et al. Somatic mutations☆16Jan 5, 2020Updated 6 years ago
- ☆18Oct 21, 2024Updated last year
- Single-cell multi-omics analysis reveals regulatory programs in clear cell renal cell carcinoma☆81Oct 29, 2024Updated last year
- Code for reproducing the Sei manuscript results☆17Jan 25, 2022Updated 4 years ago
- detecting spatial patterns of allele-specific expression☆11May 22, 2024Updated last year
- ☆10Jun 13, 2020Updated 5 years ago
- PanEffect is a JavaScript framework to explore variant effects across a pangenome. The tool has two views that allows a user to (1) expl…☆13Jan 30, 2024Updated 2 years ago
- Detect key Units in mosaic Tandem Repeats from representative reads from the same locus☆11Aug 2, 2023Updated 2 years ago
- ☆12Jan 31, 2023Updated 3 years ago
- Package to design primers for MutaSeq and related methods☆11Jan 15, 2021Updated 5 years ago
- analyses of scRNAseq and spatial transcriptomics dataset of developing human pancreas at multiple gestational stages☆10Jan 30, 2023Updated 3 years ago
- Infer the age of ancestral nodes in a tree sequence.☆24Feb 3, 2026Updated 2 weeks ago
- This repository contains HCA Benchmarking codes☆26Nov 11, 2019Updated 6 years ago
- ☆10Mar 11, 2025Updated 11 months ago
- ☆10Apr 28, 2023Updated 2 years ago
- A pipeline to process m6A-seq data and down stream analysis.☆44Aug 5, 2020Updated 5 years ago
- Detecting cancer subtypes with machine learning.☆10Feb 5, 2020Updated 6 years ago
- ☆13Apr 22, 2021Updated 4 years ago
- A detailed guide to analise and integrate small-RNASeq and RNASeq samples using miARma-Seq☆11Oct 16, 2019Updated 6 years ago
- This is the repository which contains the code that was used to generate the results and figures of the “Single-cell RNA-sequencing revea…☆12Jun 21, 2024Updated last year
- Visualize genomic data using webgl and webworkers, in an effort to provide a fluid, high-performance user experience.☆11May 24, 2024Updated last year
- An end-to-end computational pipeline for large Perturb-seq screens☆15Apr 25, 2025Updated 9 months ago
- The cattle Genotype-Tissue Expression atlas v1☆28Mar 14, 2023Updated 2 years ago
- Spatial transcriptomics of heart tissue☆28Jun 16, 2022Updated 3 years ago
- A module for working with snap files in Python☆37May 5, 2020Updated 5 years ago
- This repository contains the code for our manuscript - 'The evolution, evolvability, and engineering gene regulatory DNA'☆96Jul 11, 2023Updated 2 years ago
- Process m6A/MeRIP-seq data in a single or batch job mode☆21Apr 28, 2020Updated 5 years ago
- Graph-based Decoding for In Situ Sequencing☆10Jul 2, 2020Updated 5 years ago
- Computational framework to identify promoter sequences from RNA-seq datasets☆11Sep 27, 2023Updated 2 years ago
- ☆10Jul 2, 2024Updated last year
- Analysis repository for "Droplet-based combinatorial indexing for massive scale single-cell epigenomics"☆11Sep 30, 2019Updated 6 years ago
- Program for estimating admixture proportions and doing principal component analysis of a single NGS sample☆11Aug 15, 2024Updated last year