Minotour API, web and client code
☆30Feb 15, 2023Updated 3 years ago
Alternatives and similar repositories for minotourapp
Users that are interested in minotourapp are comparing it to the libraries listed below
Sorting:
- Determining tandem repeat lengths using raw nanopore signals.☆15Sep 11, 2023Updated 2 years ago
- ☆10Mar 11, 2025Updated 11 months ago
- ☆11May 6, 2021Updated 4 years ago
- Nanopore direct RNA basecaller☆11Oct 27, 2022Updated 3 years ago
- Hardware Accelerated Read Until☆17Sep 30, 2025Updated 5 months ago
- Adaptive haplotype assembly for efficiently leveraging high coverage in long reads☆13Sep 4, 2018Updated 7 years ago
- DNA methylation analysis downstream to Nanopolish for Oxford Nanopore DNA sequencing datasets☆30Jul 3, 2023Updated 2 years ago
- A place to collate notes and resources of our journey into porting nanopore sequencing over to accessible, portable technology.☆111May 10, 2024Updated last year
- Protobuf and gRPC specifications for the MinKNOW API☆68Oct 29, 2025Updated 4 months ago
- CLI tool for flexible and fast adaptive sampling on ONT sequencers☆194Updated this week
- Fast and scalable nanopore adaptive sampling☆35Jun 6, 2023Updated 2 years ago
- Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.☆37Jul 1, 2024Updated last year
- Scripts to install as a Bioconda package for making workflows☆18Sep 15, 2024Updated last year
- A tool to detect structural variant☆17Mar 27, 2023Updated 2 years ago
- WDL workflows for variant calling and assembly using ONT☆38Updated this week
- A computational algorithm and software tool for fast and accurate detection of gene fusion by long-read transcriptome sequencing☆21Sep 19, 2021Updated 4 years ago
- R wrapper for utilizing the SigProfilerMatrixGenerator framework☆20Jan 29, 2026Updated last month
- Variational Auto Encoders for learning binding signatures of transcription factors☆14Mar 14, 2024Updated last year
- ☆39Apr 25, 2023Updated 2 years ago
- Detect key Units in mosaic Tandem Repeats from representative reads from the same locus☆11Aug 2, 2023Updated 2 years ago
- Scotch pipeline for indel calling.☆10Nov 25, 2019Updated 6 years ago
- Ultra rapid nanopore whole genome sequencing pipeline, published in https://www.nature.com/articles/s41587-022-01221-5☆19Jun 28, 2024Updated last year
- IsoTools is a python module for Long Read Transcriptome Sequencing (LRTS) analysis.☆27Oct 6, 2023Updated 2 years ago
- Structural Variants Assessment Based on Haplotype-resolved Assemblies☆21Apr 28, 2023Updated 2 years ago
- HAT is a set of tools for calling de novo variants from whole-genome sequencing data.☆24Nov 18, 2025Updated 3 months ago
- A pipeline for Smooth-seq data analysis.☆10Sep 23, 2021Updated 4 years ago
- Python3 Read Until API implementation☆11Mar 11, 2020Updated 5 years ago
- A post sequencing QC tool for Oxford Nanopore sequencers☆106Feb 11, 2026Updated 2 weeks ago
- ☆11May 2, 2025Updated 10 months ago
- Scripts for identifying sites with differential error rates in mapped nanopore DRS data☆11Nov 27, 2020Updated 5 years ago
- ☆13Dec 16, 2024Updated last year
- R package for metabolic enzyme enrichment anaylsis☆13Oct 24, 2025Updated 4 months ago
- Expedite large-scale identification of CNVs within predefined genomic regions. Online app available for those with GP2 Tier 2 Access.☆12Jun 13, 2025Updated 8 months ago
- ☆12Apr 8, 2021Updated 4 years ago
- ☆13Feb 18, 2026Updated last week
- A single-cell RNAseq differential expression analysis approach in case-control study☆10Mar 6, 2022Updated 3 years ago
- Snakemake pipelines for nanopore sequencing data archiving and processing☆91Feb 2, 2022Updated 4 years ago
- Slow5tools is a toolkit for converting (FAST5 <-> SLOW5), compressing, viewing, indexing and manipulating data in SLOW5 format.