BioAnalyticResource / eFP-Seq_BrowserLinks
An RNA-Seq data exploration tool that shows read map coverage of a gene of interest along with a coloured "electronic fluorescent pictographic" (eFP) based on its RPKM expression level.
☆13Updated last month
Alternatives and similar repositories for eFP-Seq_Browser
Users that are interested in eFP-Seq_Browser are comparing it to the libraries listed below
Sorting:
- Pipeline for eukaryotic genome annotation based on external evidences☆13Updated 2 years ago
- Scripts for bioinformatics data processing and analysis☆12Updated last year
- ☆14Updated 2 years ago
- Direct RNA publication scripts☆11Updated 8 years ago
- All kinds of NGS analysis pipeline☆12Updated 6 years ago
- a bucket of bioinformatics scripts☆13Updated last week
- toolkit to process gtf files☆17Updated 3 years ago
- A software suite for accurate identification, annotation, translation, and feature characterization of annotate transcripts.☆19Updated 4 years ago
- GCEN: an easy-to-use toolkit for Gene Co-Expression Network analysis and lncRNAs annotation☆21Updated 3 years ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 6 months ago
- Scripts for Hill et al. (2022) doi:10.1093/molbev/msac085 🟣☆11Updated 2 years ago
- Readme☆10Updated 5 years ago
- RNA-seq analysis scripts☆15Updated 2 months ago
- RNAseq analysis with Hisat2, stringtie, and ballgown☆17Updated 6 years ago
- ☆10Updated 4 years ago
- GWAS analysis process based on EMMAX software☆13Updated last year
- Design gene specific KASP and CAPS/dCAPS primers for any species☆16Updated 3 years ago
- Automated Rice Variant calling workflow for HPC, Cloud and Desktop systems.☆13Updated last year
- Scripts for NGS processing☆17Updated 8 years ago
- Some useful bioinformatics pipelines for genomics analysis☆14Updated 4 years ago
- Repository for pipeline code☆26Updated last year
- Code associated with the manuscript "A complete reference genome improves analysis of human genetic variation".☆17Updated 2 years ago
- ☆15Updated last year
- crussmap is a faster tool to convert genome coordinates between difference reference assemblies.☆20Updated 2 years ago
- Software to assemble contigs/scaffolds into chromosomes using Hi-C data☆28Updated last year
- Guide through code for a Minimmap2 genome alignment and a seq-seq-pan pan-genome alignment with visualizations in R. The tutorial present…☆18Updated 4 months ago
- Repository☆10Updated 11 months ago
- Plot allele frequencies in VCF files☆11Updated 6 years ago
- Accurate haplotype construction and detection of selection signatures enabled by 889 high quality pig genome sequences☆13Updated 2 years ago
- Pipeline to filter whole exome vcf files and generate a report document for clinical diagnostics.☆14Updated 5 years ago