vanheeringen-lab / seq2science
Automated and customizable preprocessing of Next-Generation Sequencing data, including full (sc)ATAC-seq, ChIP-seq, and (sc)RNA-seq workflows. Works equally easy with public as local data.
☆156Updated last year
Alternatives and similar repositories for seq2science:
Users that are interested in seq2science are comparing it to the libraries listed below
- A collection of scripts and notes related to genomics and bioinformatics☆210Updated 3 weeks ago
- Tool for the Quality Control of Long-Read Defined Transcriptomes☆223Updated this week
- Download FASTQ files from SRA or ENA repositories.☆323Updated last month
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆101Updated 5 months ago
- A package for including transposable elements in differential enrichment analysis of sequencing datasets.☆248Updated 3 months ago
- classify, merge, tracking and annotation of GFF files by comparing to a reference annotation GFF☆216Updated 10 months ago
- SUPPA: Fast quantification of splicing and differential splicing☆274Updated 10 months ago
- Tool for plotting sequencing data along genomic coordinates.☆289Updated 3 months ago
- Detecting sites of genomic enrichment☆190Updated 2 years ago
- Package for fetching metadata and downloading data from SRA/ENA/GEO☆326Updated 2 months ago
- Fast, efficient RNA-Seq metrics for quality control and process optimization☆163Updated 6 months ago
- Methylation (Bisulfite-Sequencing) analysis pipeline using Bismark or bwa-meth + MethylDackel☆165Updated last week
- Web application to explore the Sequence Read Archive.☆216Updated last month
- RNA-seq workflow using STAR and DESeq2☆339Updated 9 months ago
- parallel fastq-dump wrapper☆292Updated 2 years ago
- ☆150Updated 2 years ago
- Check strandedness of RNA-Seq fastq files☆123Updated 2 years ago
- SEACR: Sparse Enrichment Analysis for CUT&RUN☆109Updated 2 years ago
- RNA-Seq analysis workflow☆104Updated 3 years ago
- zUMIs: A fast and flexible pipeline to process RNA sequencing data with UMIs☆279Updated 9 months ago
- Generate IGV style locus tracks from bigWig files in R☆159Updated 6 months ago
- Annotation-free quantification of RNA splicing. Yang I. Li, David A. Knowles, Jack Humphrey, Alvaro N. Barbeira, Scott P. Dickinson, Hae …☆214Updated 11 months ago
- Reference-guided transcript discovery and quantification for long read RNA-Seq data☆208Updated this week
- Application for making ENCODE Blacklists☆303Updated 4 years ago
- Iso-Seq - Scalable De Novo Isoform Discovery from Single-Molecule PacBio Reads☆212Updated 3 weeks ago
- Transcription factor Occupancy prediction By Investigation of ATAC-seq Signal☆210Updated 3 months ago
- HiCExplorer is a powerful and easy to use set of tools to process, normalize and visualize Hi-C data.☆246Updated 5 months ago
- A short tutorial on how to use RSEM☆136Updated 5 years ago
- Discovering known and novel miRNAs from small RNA sequencing data☆147Updated 8 months ago
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆124Updated 5 years ago