LUMC / fastqsplitterLinks
Splits fastq files evenly
☆23Updated 5 years ago
Alternatives and similar repositories for fastqsplitter
Users that are interested in fastqsplitter are comparing it to the libraries listed below
Sorting:
- Long-read Isoform Quantification and Analysis☆38Updated 9 months ago
- ☆38Updated 2 years ago
- A Python library to visualize and analyze long-read transcriptomes☆64Updated 8 months ago
- Ultra-fast 5' and 3' demultiplexer☆28Updated last year
- SingleCell Nanopore sequencing data analysis☆62Updated 7 months ago
- ☆12Updated 3 weeks ago
- Concurrent identification of m6A and m5C modifications in individual molecules from nanopore sequencing☆42Updated last year
- IsoTools is a python module for Long Read Transcriptome Sequencing (LRTS) analysis.☆27Updated 2 years ago
- Long read to rMATS☆32Updated 2 years ago
- trackplot is a tool for visualizing various next-generation sequencing (NGS) data, including DNA-seq, RNA-seq, single-cell RNA-seq and fu…☆99Updated last month
- isoCirc☆10Updated 2 years ago
- Hi-C Interaction Frequency Inference (HIFI): High-resolution estimation of DNA-DNA interaction frequency from Hi-C data☆24Updated 3 years ago
- A Library to Explore Chromatin Interaction Patterns for Topologically Associating Domains☆45Updated 3 years ago
- ☆38Updated last year
- An R package for estimating poly(A)-tail lengths in Oxford Nanopore RNA and DNA reads.☆55Updated last year
- Find and characterise transposable element insertions☆20Updated 2 years ago
- A script to make downloading of SRA/GEO data easier☆33Updated 2 years ago
- Workflow for Nanopore Sequencing of 10x single cell libraries☆19Updated 9 months ago
- ☆64Updated 3 months ago
- ☆34Updated last month
- Digenome-toolkit ver2.☆16Updated 4 years ago
- Benchmarking long-read RNA-seq analysis tools☆27Updated 10 months ago
- EasyFuse is a pipeline for accurate fusion gene detection from RNA-seq data.☆62Updated 2 months ago
- A tool for accurately detecting actively translating ORFs from Ribo-seq data☆39Updated 11 months ago
- EM based transcript abundance from nanopore reads mapped to a transcriptome with minimap2☆64Updated last year
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆41Updated 4 months ago
- IDR☆31Updated 2 years ago
- A Perl/R pipeline for plotting metagenes☆37Updated 4 years ago
- Comprehensive analysis of small RNA sequencing data☆34Updated 7 months ago
- RepEnrich2 is an updated method to estimate repetitive element enrichment using high-throughput sequencing data.☆41Updated 3 years ago