NGS Data Analysis Textbook Version 2 (Disease Genome Analysis)
☆43May 7, 2021Updated 5 years ago
Alternatives and similar repositories for ngsdat2
Users that are interested in ngsdat2 are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Step by step tutorial for CAGE analysis☆10Sep 18, 2025Updated last year
- RNAseq pipeline centered on Salmon☆29Nov 21, 2024Updated last year
- SkewC a novel quality-assessment method to identify poor quality single-cells in scRNA-seq experiments. The method relies on the measure …☆10Aug 2, 2023Updated 3 years ago
- Localization of transcribed enhancers and quntification of their usage from the initiation sites of bidirectionally transcribed loci☆14Dec 19, 2024Updated last year
- Common Workflow Language definition files for workflows introduced in DAT2☆11May 23, 2022Updated 4 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- DBCLS RDFizing database guidelines☆16Aug 31, 2024Updated 2 years ago
- ☆125Sep 25, 2026Updated last week
- PythonによるシングルセルRNA-seq解析。☆23Dec 16, 2022Updated 3 years ago
- 生命科学者のためのDr.Bonoデータ解析実践道場☆10Sep 19, 2019Updated 7 years ago
- ☆14Dec 16, 2022Updated 3 years ago
- ☆11Mar 16, 2022Updated 4 years ago
- iDEP: integrated Differential Expression & Pathway analysis☆14Mar 1, 2019Updated 7 years ago
- Port of symphony algorithm of single-cell reference atlas mapping to Python☆34May 19, 2026Updated 4 months ago
- Porting of samtools-ruby to BioRuby. Binder of samtools for ruby, on the top of FFI -from original project-☆34Sep 20, 2019Updated 7 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- ☆16Apr 2, 2024Updated 2 years ago
- GTS: Genome Transformation Subprograms☆15Feb 25, 2023Updated 3 years ago
- Data/analysis repository for "Interrogation of human hematopoiesis..." paper☆21Jul 9, 2019Updated 7 years ago
- The Single-Cell Pathology Landscape of Breast Cancer☆28Jan 14, 2020Updated 6 years ago
- Common Workflow Language tools and workflows by Pitagora-Network☆32Nov 8, 2022Updated 3 years ago
- Web app for automated, systematic, and integrated RNA-seq differential expression analysis☆16May 1, 2026Updated 5 months ago
- A (very) fast program for getting statistics about a fastq file, the way I need them, written in Rust☆34Jul 27, 2026Updated 2 months ago
- Ruby UCSC API: An API for the UCSC Genome Database☆19Jul 21, 2022Updated 4 years ago
- ☆42Jul 3, 2025Updated last year
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- Fast and flexible tool for reading, modifying and writing biological sequences☆18Feb 4, 2026Updated 8 months ago
- Materials for tutorial at ajacs68 (Japanese)☆32Jan 17, 2018Updated 8 years ago
- Piranha is a peak-caller for CLIP- and RIP-seq data☆21Feb 7, 2018Updated 8 years ago
- Dissecting the effects of DNA copy number variations on transcriptional programs at single-cell resolution☆14Feb 13, 2026Updated 7 months ago
- Count HLA alleles in single-cell RNA-seq data☆64Nov 5, 2021Updated 4 years ago
- Scripts for the analysis of TT-seq and DRB/TT-seq data.☆12Mar 11, 2020Updated 6 years ago
- Fuji plot—a circos representation of multiple GWAS results—☆99May 29, 2025Updated last year
- Imaging Mass Cytometry (IMC) file type support for napari☆13Jul 8, 2026Updated 2 months ago
- ☆52Jun 25, 2024Updated 2 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- A RubyGem that provides common datasets☆33Sep 26, 2026Updated last week
- 「生物ネットワーク解析」の補足資料☆26Feb 20, 2025Updated last year
- ☆26Sep 17, 2026Updated 2 weeks ago
- Statistical analysis for spatial omics data☆11Jul 30, 2022Updated 4 years ago
- FINSURF is a tool designed to analyse lists of sequences variants in the human genome.☆12Oct 24, 2022Updated 3 years ago
- A docker image for single-cell analysis☆106Sep 10, 2026Updated 3 weeks ago
- Scripts used to generate the data/figures contained in "Single Cell Transcriptomics Reveals Cell Type Specific Diversification in Human H…☆15Mar 10, 2023Updated 3 years ago