☆15Jun 13, 2022Updated 4 years ago
Alternatives and similar repositories for EBI_cancer_workshop_SNV
Users that are interested in EBI_cancer_workshop_SNV are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- hands-on for NGS/SNParray CNV call trainning☆19Jun 13, 2022Updated 4 years ago
- EBI cancer workshop course materials☆21May 9, 2022Updated 4 years ago
- Materials for ShinyConf 2023 talk: Debugging With Shiny☆13May 10, 2023Updated 3 years ago
- Multifactorial modeling of response to checkpoint inhibitor immunotherapy from tumor, immune, and clinical features☆17Jun 29, 2018Updated 8 years ago
- GitHub for the SIB courses NGS - Genome variant analysis☆28Jun 22, 2026Updated 2 weeks 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.
- Nextflow hackathon 2017 projects☆10Sep 28, 2017Updated 8 years ago
- Nextflow workflows to assign Salmonella serotype based on Genome similarity using MASH, SOURMASH and KMA.☆13Jul 2, 2026Updated last week
- Tools to handle reads sequenced with unique molecular identifiers (UMIs).☆30Jun 26, 2017Updated 9 years ago
- ☆25May 22, 2026Updated last month
- Conveniently perform ASCAT copy-number analysis from Tumor-Normal or Tumor only BAM files in R☆12Dec 6, 2021Updated 4 years ago
- Fast implementation of the Neighbour-Joining method for phylogenetic inference☆20Sep 10, 2024Updated last year
- Northern Arizona SNP Pipeline☆20Oct 29, 2024Updated last year
- PuntSeq - Chasing the microbial diversity of Cambridge's freshwater☆20Nov 12, 2020Updated 5 years ago
- pipeline for dog WGS alignment☆15Jun 27, 2023Updated 3 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.
- RADIA: RNA and DNA Integrated Analysis for Somatic Mutation Detection☆29Oct 1, 2020Updated 5 years ago
- Contribution of systemic and somatic factors to clinical response and resistance in urothelial cancer: an exploratory multi-omic analysis☆24Oct 31, 2017Updated 8 years ago
- Book: Pratitioner's Guide to Data Science (https://scientistcafe.com/ids/)☆42Jul 4, 2023Updated 3 years ago
- BACTpipe: An assembly and annotation pipeline for bacterial genomics☆20Dec 3, 2024Updated last year
- Data Structures for Bioinformatics - LM Bioinformatics - University of Rome Tor Vergata☆12Feb 27, 2026Updated 4 months ago
- A deme-based, spatially explicit model of intra-tumour population genetics☆21Jan 28, 2025Updated last year
- Materials for the Training and Engagement Website☆25Jan 12, 2024Updated 2 years ago
- data repo for fusions found in human genomes and transcriptomes☆10Jan 21, 2024Updated 2 years ago
- Bayesian inference of clone-specific gene expression estimates by integrating single-cell RNA-seq and single-cell DNA-seq data☆37Dec 15, 2020Updated 5 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.
- Sample Level Analysis of Pathway Alteration Enrichments☆10Jan 21, 2019Updated 7 years ago
- Dashboard to explore my liked tweets (up to April 2023), and give links to resources.☆25Feb 5, 2026Updated 5 months ago
- Scripts and files for the annual Short Read Analysis Workshop☆14Updated this week
- Package to create MOVIE Plots☆12Oct 31, 2019Updated 6 years ago
- Parallel merging, squaring off and ensemble calling for genomic variants☆20Sep 17, 2019Updated 6 years ago
- Workshop: Using R/tidyverse to analyze & visualize gapminder/processed transcriptomics data!☆13Sep 12, 2025Updated 9 months ago
- Machine learning use cases for teaching☆13Jul 12, 2017Updated 8 years ago
- Consistent Clusters for scRNA-seq☆11Oct 6, 2021Updated 4 years ago
- Welcome to the website and github repository for the Genome Analysis Module. This website will guide the learning experience for trainees…☆26Nov 14, 2022Updated 3 years ago
- Simple, predictable pricing with DigitalOcean hosting • AdAlways know what you'll pay with monthly caps and flat pricing. Enterprise-grade infrastructure trusted by 600k+ customers.
- Single Cell Caller (SCcaller) - Identify single nucleotide variations (SNVs) from single cell sequencing data☆39Nov 27, 2024Updated last year
- ☆27Dec 29, 2020Updated 5 years ago
- Tutorial on using E-utilities☆25Mar 20, 2025Updated last year
- UZH BIO392: Bioinformatics of Sequence Variation Course Repository☆15May 29, 2026Updated last month
- a python library for working with flow cytometry data.☆14May 11, 2015Updated 11 years ago
- Documenting usage and experience with bioinformatic tools☆40Sep 11, 2015Updated 10 years ago
- Secure Cloud Object REsource: file transfer microservice☆20May 25, 2026Updated last month