crazyhottommy / awesome-long-reads
tools and notes for long reads analysis
☆19Updated 8 months ago
Related projects ⓘ
Alternatives and complementary repositories for awesome-long-reads
- This package provides a function to reformat lists of genome coverage files, such as bigWig of bam files, into the directory structure of…☆28Updated 6 months ago
- Scripts to import your FeatureCounts output into DEXSeq☆31Updated 6 years ago
- SingleCell Nanopore sequencing data analysis☆52Updated 3 weeks ago
- Differential ATAC-seq toolkit☆27Updated 11 months ago
- Differential expression and allelic analysis, nonparametric statistics☆27Updated last year
- Detecting intron retention from RNA-Seq experiments☆53Updated 4 months ago
- Bioinformatics one-liner for 100 days☆43Updated 7 months ago
- ☆9Updated 4 years ago
- OUTRIDER: OUTlier in RNA-seq fInDER is an R-based framework to find aberrantly expressed genes in RNA-seq data☆50Updated 3 months ago
- RNA-seq data comprehensive data analysis toolbox☆19Updated 2 years ago
- workshop website on readthedocs☆19Updated last week
- Flexible and efficient parsing, interpreting and editing of sequencing reads☆41Updated last month
- Snakemake pipeline for running MAJIQ☆19Updated 11 months ago
- Pairtree is a method for reconstructing cancer evolutionary history in individual patients, and analyzing intratumor genetic heterogeneit…☆37Updated 7 months ago
- A collection of code snippets for different tasks☆9Updated last year
- Flexible Bayesian inference of mutational signatures☆33Updated last year
- GREAT Analysis - Functional Enrichment on Genomic Regions☆85Updated 3 months ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆32Updated 3 years ago
- A template repository for Snakemake pipepline(s) and a python command-line toolkit.☆27Updated last month
- processes GoT amplicon data and generates a table of metrics☆26Updated 2 years ago
- A Python library to visualize and analyze long-read transcriptomes☆57Updated 8 months ago
- Genomic coordinates of problematic genomic regions as GRanges☆28Updated 11 months ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆41Updated 2 years ago
- An R interface to the MEME Suite☆46Updated last month
- ☆20Updated 2 months ago
- RepEnrich2 is an updated method to estimate repetitive element enrichment using high-throughput sequencing data.☆36Updated 2 years ago
- Benchmarking long-read RNA-seq analysis tools☆25Updated 9 months ago
- ☆21Updated 2 weeks ago
- Sigflow: Streamline Analysis Workflows for Mutational Signatures, https://github.com/ShixiangWang/sigflow/pkgs/container/sigflow☆26Updated last month
- Compendium to "A Systematic Evaluation of Single Cell RNA-Seq Analysis Pipelines"☆53Updated 3 years ago