vanheeringen-lab / seq2scienceLinks
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.
☆165Updated 4 months ago
Alternatives and similar repositories for seq2science
Users that are interested in seq2science are comparing it to the libraries listed below
Sorting:
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆106Updated 4 months ago
- A collection of scripts and notes related to genomics and bioinformatics☆219Updated this week
- Detecting sites of genomic enrichment☆194Updated 2 years ago
- Tool for the Quality Control of Long-Read Defined Transcriptomes☆239Updated last week
- Reference-guided transcript discovery and quantification for long read RNA-Seq data☆219Updated last month
- SUPPA: Fast quantification of splicing and differential splicing☆281Updated last year
- Fast, efficient RNA-Seq metrics for quality control and process optimization☆175Updated 11 months ago
- ☆155Updated 2 years ago
- dN/dS methods to quantify selection in cancer and somatic evolution☆225Updated 4 months ago
- Check strandedness of RNA-Seq fastq files☆125Updated 3 years ago
- Discovering known and novel miRNAs from small RNA sequencing data☆154Updated last year
- Download FASTQ files from SRA or ENA repositories.☆344Updated 3 months ago
- Tool for plotting sequencing data along genomic coordinates.☆319Updated 3 months ago
- A short tutorial on how to use RSEM☆138Updated 5 years ago
- A package for including transposable elements in differential enrichment analysis of sequencing datasets.☆263Updated 3 weeks ago
- Pipeline to fetch metadata and raw FastQ files from public databases☆181Updated 2 months ago
- tools for working with Bisulfite Sequencing data while preserving reads intrinsic dependencies☆168Updated 4 months ago
- Suite of motif tools, including a motif prediction pipeline for ChIP-seq experiments. See full GimmeMotifs documentation for detailed in…☆120Updated this week
- Generate IGV style locus tracks from bigWig files in R☆171Updated 11 months ago
- Analyze your RNA sequencing data without writing a single line of code☆139Updated 4 months ago
- Web application to explore the Sequence Read Archive.☆217Updated 2 months ago
- Fast alignment and preprocessing of chromatin profiles☆204Updated 2 weeks ago
- An R package to Identify, Annoatate and Visialize Isoform Switches with Functional Consequences (from RNA-seq data)☆117Updated 8 months ago
- Pipeline to find aberrant events in RNA-Seq data, useful for diagnosis of rare disorders☆155Updated 3 weeks ago
- RNA-Seq analysis workflow☆105Updated 4 years ago
- Download sequencing data and metadata from GSA, SRA, ENA, and DDBJ databases.☆214Updated last month
- SEACR: Sparse Enrichment Analysis for CUT&RUN☆114Updated 2 years ago
- minimal example implementations for bioinformatics workflow managers☆279Updated 3 years ago
- Annotation-free quantification of RNA splicing. Yang I. Li, David A. Knowles, Jack Humphrey, Alvaro N. Barbeira, Scott P. Dickinson, Hae …☆224Updated last year
- Nanopore RNA-Seq data from the Singapore Nanopore-Expression Project☆138Updated last month