Find bimodal, unimodal, and multimodal features in your data
☆27Oct 26, 2018Updated 7 years ago
Alternatives and similar repositories for anchor
Users that are interested in anchor are comparing it to the libraries listed below
Sorting:
- A scientific publication, describing a way to improve microscopy. This repository hosts everything you need to reproduce our results. Rea…☆13Jun 22, 2024Updated last year
- python (cython) wrapper for https://github.com/ryanlayer/giggle for fast interval searching of huge datasets.☆15Feb 13, 2018Updated 8 years ago
- A phase-aware pharmacogenomic diplotyper for PacBio datasets☆20Dec 9, 2025Updated 2 months ago
- LAAVA: Long-read AAV Analysis☆13Dec 9, 2025Updated 2 months ago
- Lab notebook for people who like the command line.☆11Jun 19, 2024Updated last year
- Introduction to Python Programming☆11Mar 31, 2020Updated 5 years ago
- Code for simulating a multi-view acquisition including attenuation, convolution, reduced sampling and poission noise☆13Jun 14, 2022Updated 3 years ago
- Peak calling tool for CLIP-seq data☆14Apr 7, 2021Updated 4 years ago
- A small, auxiliary index to massively improve parallel fastq parsing☆31Feb 12, 2026Updated 2 weeks ago
- Things we use regularly☆29Aug 5, 2025Updated 6 months ago
- edit distance sequence tags and helpers☆12Feb 4, 2021Updated 5 years ago
- Command line tools for IntSpan related bioinformatics operations☆12Apr 9, 2025Updated 10 months ago
- Sweep-line algorithm for genomic features. Detect overlaps on large files w/ minimal memory.☆10Sep 13, 2011Updated 14 years ago
- Cromwell output organizer☆13May 18, 2021Updated 4 years ago
- Explore and analyze biological sequence data☆17Aug 1, 2024Updated last year
- CLI to automate Nextflow pipeline testing☆12Dec 15, 2025Updated 2 months ago
- Python package for optical flow estimation☆15Dec 25, 2022Updated 3 years ago
- Examples of kallisto + sleuth☆11May 18, 2017Updated 8 years ago
- An R Interface to Large Language Models☆27Sep 21, 2025Updated 5 months ago
- zsh plugin to list up EC2 instances and ssh login the instances.☆11Apr 10, 2018Updated 7 years ago
- Quantitative analysis of cell motility behaviors☆13Feb 21, 2025Updated last year
- Robust individual and aggregate checksums for nucleotide sequences☆17Feb 8, 2026Updated 3 weeks ago
- ☆15Jun 3, 2025Updated 8 months ago
- robust matching of small variant datasets using flexible scoring schemes☆11Mar 26, 2020Updated 5 years ago
- ☆13Sep 5, 2017Updated 8 years ago
- Split a BAM file by haplotype support☆16Dec 13, 2017Updated 8 years ago
- Multithreaded read analysis☆23Feb 19, 2026Updated last week
- Benchmarking variant calling in polyploids☆15Nov 26, 2021Updated 4 years ago
- FUSE filesystem for the DNAnexus storage system☆13Jan 26, 2026Updated last month
- Library for visualising genomic features in Python.☆15May 12, 2017Updated 8 years ago
- ☆20Nov 15, 2025Updated 3 months ago
- a toolbox for metabolomic data analysis, visualization and ‘omic’ integration☆13Jun 21, 2018Updated 7 years ago
- ☆16Jan 15, 2025Updated last year
- Rust UMI Directional Adjacency Deduplicator☆15Nov 25, 2019Updated 6 years ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆35Jul 5, 2021Updated 4 years ago
- 🎯 Generate DNA sequences with specified amino acid, codon, and k-mer frequencies☆17Jan 23, 2023Updated 3 years ago
- Allele-Specific Quantification of Structural Variations in Cancer Genomes☆18Mar 5, 2019Updated 6 years ago
- Bedfile perturbation tool☆17Sep 29, 2025Updated 5 months ago
- A simple tool to fix PacBio fasta/q that was not properly split into subreads☆16Jun 10, 2021Updated 4 years ago