friedue / course_RNA-seq2017Links
β12Updated 7 years ago
Alternatives and similar repositories for course_RNA-seq2017
Users that are interested in course_RNA-seq2017 are comparing it to the libraries listed below
Sorting:
- DRAGEN Tumor/Normal workflow post-processingβ22Updated last year
- π An R package of RNA-seq workflowβ16Updated 3 years ago
- DriverPowerβ26Updated 5 months ago
- A multi-method comparative bioinformatics pipeline to detect and study circRNAs from RNA-seq dataβ15Updated 5 years ago
- A small R package to make sequencing read coverage plots in R.β38Updated 2 years ago
- Filter and prioritize fusion callsβ20Updated 8 months ago
- Relative Abundance of Transcripts: An R package for the detection of Differential Transcript isoform Usage.β34Updated 3 years ago
- Make rapid visualizations of RNA-seq data in Rβ19Updated 5 years ago
- CNV analysis workflow code for the manuscriptβ13Updated 5 years ago
- A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites.β29Updated 10 months ago
- A tidy interface for coverage analysisβ29Updated 5 years ago
- β9Updated 5 years ago
- Differential ATAC-seq toolkitβ27Updated last year
- RNA-seq quantifications: gene expression responses to human rhinovirus infection for 6 asthmatic and 6 non-asthmatic donors (SRP046226)β19Updated 7 years ago
- Tool for parsing outputs from fusion detection tools. Part of a nf-core/rnafusion pipeline. Checkout a live demo at https://matq007.githuβ¦β26Updated last week
- Provides Quality Control of sequencing samples by deducing if there is batch effect and adjusts for it.β35Updated last year
- HOT regions paperβ11Updated 6 years ago
- Merge fastq files split over lanesβ20Updated 7 years ago
- β23Updated 4 years ago
- Create a cromphensive report of DEG list coming from any analysis of RNAseq dataβ26Updated last year
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer driversβ15Updated 6 years ago
- A set of tools to annotate VCF files with expression and readcount dataβ29Updated 3 months ago
- Interactive R package to quantify, analyse and visualise alternative splicingβ37Updated this week
- AnaLysis routines for ePigenomicS data - π« Bioconductor projectβ16Updated last year
- Isoform co-usage networks from single-cell RNA-seq dataβ16Updated last year
- The official repository of the Bioconductor 2019 Conference Workshopsβ25Updated 2 years ago
- R package for DNA methylation analysisβ18Updated 10 months ago
- Analysis and Interpretation of Bulk RNA-Seq Data using Bioconductorβ22Updated this week
- Bulk RNA-seq Data Processing, Quality Control, and Downstream Analysis Pipelineβ21Updated 5 months ago
- Scripts and software supplement for "Gene-level differential analysis at transcript-level resolution" by Yi, Pimentel, Bray and Pachterβ19Updated 7 years ago