☆35Feb 11, 2026Updated 4 months ago
Alternatives and similar repositories for onco_lnc
Users that are interested in onco_lnc are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆11Aug 21, 2018Updated 7 years ago
- ☆78Mar 6, 2014Updated 12 years ago
- MAGERI - Assemble, align and call variants for targeted genome re-sequencing with unique molecular identifiers☆22May 8, 2017Updated 9 years ago
- commandline manipulation of genomic variants and NGS reads☆19Sep 6, 2024Updated last year
- ☆11Jul 13, 2018Updated 7 years ago
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- Bioconductor2017 workshop - Analysis of single-cell RNA-seq data: Normalization, dimensionality reduction, clustering, and lineage infere…☆11Aug 4, 2017Updated 8 years ago
- Mutation Spectra Analysis☆10Mar 15, 2018Updated 8 years ago
- Sample Level Analysis of Pathway Alteration Enrichments☆10Jan 21, 2019Updated 7 years ago
- QC3, a quality control tool designed for DNA sequencing data for raw data, alignment, and variant calling.☆32May 31, 2016Updated 10 years ago
- ☆14Aug 30, 2025Updated 9 months ago
- R package for Enrichment Depletion Logos (EDLogos) and String Logos☆27Dec 12, 2018Updated 7 years ago
- Bioinformatic pipeline for identifying dsDNA breaks by marker based incorporation, such as breaks induced by designer nucleases like Cas9…☆22Jul 26, 2025Updated 10 months ago
- An R client for broads firehose pipeline, providing TCGA data sets☆60Jun 25, 2019Updated 6 years ago
- ☆62Aug 4, 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.
- Causal Variant Evidence Mapping with Non-parametric resampling☆12Dec 16, 2020Updated 5 years ago
- ☆11Jun 26, 2020Updated 5 years ago
- Utilities for analyzing mutations and neoepitopes in patient cohorts☆20Jun 7, 2018Updated 8 years ago
- Finding cryptic relationships to boost disease gene detection☆12May 31, 2023Updated 3 years ago
- picking up low allelic-fraction, somatic variants from tumor samples☆14Jan 4, 2018Updated 8 years ago
- An awk-like VCF parser☆55Jan 2, 2024Updated 2 years ago
- Miscellaneous documents☆13Dec 3, 2025Updated 6 months ago
- ☆13May 16, 2016Updated 10 years ago
- Analysis Framework for Biological Data from High Throughput Experiments☆34Aug 24, 2016Updated 9 years ago
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- Allele frequency filtering for Mendelian variant discovery☆18Sep 27, 2016Updated 9 years ago
- Examples of kallisto + sleuth☆11May 18, 2017Updated 9 years ago
- A novel PSSM based software for predicting class I peptide-HLA binding affinity☆16Feb 24, 2017Updated 9 years ago
- ☆14Jul 18, 2021Updated 4 years ago
- Core utilities for single-cell RNA-seq☆13Apr 6, 2026Updated 2 months ago
- Analysis tools for longevity research☆22Jul 23, 2017Updated 8 years ago
- jupyter notebook; perform differential gene expression analysis using DESeq2 on TCGA RNAseq data☆33Mar 1, 2019Updated 7 years ago
- goleft is a collection of bioinformatics tools distributed under MIT license in a single static binary☆227Sep 18, 2025Updated 8 months ago
- pipelines to process scRNA-seq data☆12Jan 11, 2021Updated 5 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.
- Library for indexing VCF files for random access searches by rsID☆17Mar 2, 2026Updated 3 months ago
- Workshop content for http://dib-training.readthedocs.org/en/pub/2016-01-13-adv-beg-shell.html☆13Feb 23, 2018Updated 8 years ago
- Telomerecat: The telomere computational analysis tool☆22Aug 4, 2021Updated 4 years ago
- Provide R access to the NCI Genomic Data Commons portal.☆90Apr 29, 2026Updated last month
- An R Interface to the ImmuneSpace database portal☆24Nov 28, 2023Updated 2 years ago
- Syllabus and materials for bioinformatics lecture + lab☆21Apr 23, 2015Updated 11 years ago
- reproduce the functional enrichment analysis presented in GTEx paper using clusterProfiler/DOSE☆33Jul 6, 2021Updated 4 years ago