zhongzhd / ont_m6a_detectionLinks
☆10Updated 5 months ago
Alternatives and similar repositories for ont_m6a_detection
Users that are interested in ont_m6a_detection are comparing it to the libraries listed below
Sorting:
- nanoNOMe (Nucleosome Occupancy and Methylome nanopore sequencing) Analysis☆18Updated 2 years ago
- A pipeline for Smooth-seq data analysis.☆10Updated 3 years ago
- The R package "sarlacc" contains a pipeline to analyse nanopore sequencing data. It trims adapter sequences, retrieves optional UMI's, cl…☆14Updated 6 years ago
- Reconstructs complex variation using Bionano optical mapping data and breakpoint graph data☆18Updated last year
- DNAscan2 is a fast and efficient bioinformatics pipeline that allows for the analysis of DNA Next Generation sequencing data, requiring v…☆14Updated last year
- End-guided RNA assembler☆15Updated last week
- Scripts and notebooks used in Akgol Oksuz et al. paper☆11Updated 4 years ago
- single-cell analysis workflows for double phosphoramidite barcode and UMI Correction (scCOLOR-seq)☆13Updated 2 years ago
- Whole genome workflows☆12Updated 9 months ago
- Analyse RNA feature distributions.☆16Updated 8 months ago
- Scripts for identifying sites with differential error rates in mapped nanopore DRS data☆11Updated 4 years ago
- An integrated computational framework for comprehensive transcriptome analyses with Nanopore direct-RNA sequencing data☆14Updated 3 months ago
- Computational analyses of WGS, mate-pair, RNA-seq, Hi-C and Capture-C data from highly rearranged balancer chromosomes in Drosophila mela…☆10Updated 5 years ago
- Package to design primers for MutaSeq and related methods☆11Updated 4 years ago
- ☆22Updated last month
- R package specialized in HLA typing clustering and visualization based on specific similarity metrics☆13Updated 5 years ago
- Benchmarking long-read RNA-seq analysis tools☆27Updated 6 months ago
- Comprehensive and scalable differential splicing analyses☆17Updated 5 months ago
- Joint normalization of two Hi-C matrices, visualization and detection of differential chromatin interactions. See multiHiCcompare for the…☆22Updated 2 years ago
- General Use Scripts and Helper functions☆16Updated 7 years ago
- Workflow for Sequenza, cellularity and ploidy☆20Updated last week
- Ultra rapid nanopore whole genome sequencing pipeline, published in https://www.nature.com/articles/s41587-022-01221-5☆19Updated last year
- Scatterbar - data visualization for proportional data across many spatially resolved coordinates☆11Updated 5 months ago
- ☆19Updated 2 years ago
- Long read to rMATS☆32Updated 2 years ago
- isoCirc☆10Updated last year
- Two pass alignment for long reads☆22Updated 4 years ago
- R Package for phasing of single cell Strand-seq data☆10Updated 7 months ago
- HAT is a set of tools for calling de novo variants from whole-genome sequencing data.☆24Updated last year
- CircSplice☆12Updated 6 years ago