collection of small scripts or how-tos that don't fall under a separate project
☆21Oct 18, 2017Updated 8 years ago
Alternatives and similar repositories for junkdrawer
Users that are interested in junkdrawer are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Polygenic score calculation from VCF in Nim.☆15Nov 22, 2020Updated 5 years ago
- Normalization and difference calling for Next Generation Sequencing (NGS) data via joint multinomial modeling.☆11May 21, 2026Updated last month
- A Swiss army knife for genome projects☆15Aug 13, 2013Updated 12 years ago
- Online material and code base for the article Coordinates and Intervals in Graph Based Reference Genomes☆11May 2, 2017Updated 9 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Jun 4, 2024Updated 2 years ago
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- Shape analysis of high-throughput data☆19Feb 24, 2016Updated 10 years ago
- Metagenomics-focused BAM file manipulation☆15Jul 8, 2019Updated 7 years ago
- python stuff I use☆20Feb 16, 2026Updated 5 months ago
- Tools for producing pseudo-cgh of next-generation sequencing data☆18Sep 5, 2016Updated 9 years ago
- An approximate sequence pattern matcher for FASTQ/FASTA files.☆32Jan 22, 2016Updated 10 years ago
- Simulation and power calculations for time-to-event trials☆18May 21, 2020Updated 6 years ago
- Demonstrating the PRoot program☆11Jul 29, 2016Updated 9 years ago
- Variant Alert!, a framework to monitor every significant alteration in variant classification and gene-disease association between two ve…☆14Jul 19, 2021Updated 4 years ago
- Spec for R coffee-script☆17Nov 26, 2013Updated 12 years ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- Peakzilla is a self-learning algorithm to identify transcription factor binding sites from ChIP-seq data. I would be very happy if you tr…☆21Aug 18, 2025Updated 10 months ago
- Rcount: simple and flexible RNA-Seq read counting☆12May 19, 2022Updated 4 years ago
- ☆15Aug 28, 2014Updated 11 years ago
- Spiritual successor to picard for sequencing qc☆55Updated this week
- IPython Notebook Theme. Base16 default colors, VIM mode by default☆45Jun 27, 2014Updated 12 years ago
- Django backend to varapp☆20Feb 9, 2017Updated 9 years ago
- RNA-Skim: a rapid method for RNA-Seq quantification at transcript level☆19Sep 3, 2017Updated 8 years ago
- Flexible genotype query among 30,000+ samples whole-genome☆95Sep 4, 2019Updated 6 years ago
- Streaming relation (overlap, distance, KNN) of (any number of) sorted genomic interval sets. #golang☆47Jun 16, 2026Updated last month
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- ☆15Aug 14, 2020Updated 5 years ago
- A demo implementation of Succinct de Bruijn Graphs.☆25Jun 30, 2013Updated 13 years ago
- ☆15Jun 29, 2021Updated 5 years ago
- A configurable de novo assembly pipeline☆30Jun 29, 2016Updated 10 years ago
- Application for hosting gene expression and ontology data with Shiny☆17Jan 8, 2018Updated 8 years ago
- ATAC_seq Workshop☆13Feb 16, 2018Updated 8 years ago
- Build and Deliver Software with Containers☆34Jun 12, 2026Updated last month
- Miniature LIMS and workflow manager for bioinformatics☆41Aug 17, 2011Updated 14 years ago
- What's The Function of these genes?☆22Mar 17, 2017Updated 9 years ago
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants☆25Mar 17, 2016Updated 10 years ago
- High-performance error correction for Illumina resequencing data☆75May 31, 2016Updated 10 years ago
- SNAPR: a bioinformatics pipeline for efficient and accurate RNA-seq alignment and analysis☆25Apr 7, 2015Updated 11 years ago
- Genomics database manager☆25Mar 3, 2014Updated 12 years ago
- Fast but inaccurate adapter trimmer for Illumina reads☆16Mar 17, 2022Updated 4 years ago
- See:☆18Jan 19, 2015Updated 11 years ago
- ☆11Jul 16, 2018Updated 8 years ago