JEFworks-Lab / scatterbarLinks
Scatterbar - data visualization for proportional data across many spatially resolved coordinates
☆11Updated 10 months ago
Alternatives and similar repositories for scatterbar
Users that are interested in scatterbar are comparing it to the libraries listed below
Sorting:
- A Nextflow pipeline to align, merge, and organize large PhIP-Seq datasets☆12Updated 11 months ago
- FunctionaL Omics Processing platform☆13Updated last year
- Smooth-quantile Normalization Adaptation for Inference of co-expression Links☆16Updated 2 years ago
- ☆17Updated 6 months ago
- A Quality Control filter and parser for NCBI BLAST XML results.☆17Updated 5 years ago
- A p-value-free method for controlling false discovery rates in high-throughput biological data with two conditions☆41Updated 3 years ago
- ☆20Updated 8 months ago
- rnalib: a python-based transcriptomics library☆11Updated this week
- ☆19Updated 2 years ago
- ☆10Updated 10 months ago
- tspex: tissue-specificity calculator☆36Updated 2 years ago
- ☆13Updated 2 years ago
- ORF Quantification pipeline for Alternative Splicing☆16Updated 4 years ago
- ☆18Updated last year
- Predicting TF sequence-specificity similarity with weighted alignments☆13Updated 6 years ago
- Nanopore Real-Time Analysis Tool☆16Updated last year
- Benchmarking long-read RNA-seq analysis tools☆27Updated 11 months ago
- Efficient retrieval, download, and unification of genomic data from leading biodiversity databases☆17Updated last week
- pathway based data integration and visualization☆43Updated 9 months ago
- Importing and manipulating Hi-C data in R☆11Updated 6 months ago
- ExTraMapper is a tool to find Exon and Transcript-level Mappings of a given pair of orthologous genes between two organisms using sequenc…☆11Updated 3 years ago
- The R package "sarlacc" contains a pipeline to analyse nanopore sequencing data. It trims adapter sequences, retrieves optional UMI's, cl…☆15Updated 6 years ago
- NeoFuse is a user-friendly pipeline for the prediction of fusion neoantigens from tumor RNA-seq data.☆20Updated 3 years ago
- Analyze antibody repertoires and discover new V genes from high-throughput sequencing reads☆16Updated 2 years ago
- Analyse RNA feature distributions.☆18Updated last year
- Scripts used in the analysis of C elegans dRNAseq data☆14Updated last year
- FREE Divergence Error-Correcting DNA Barcodes☆10Updated 7 years ago
- Rapid and accurate ancestry inference using SNVs.☆28Updated 5 months ago
- Whole genome workflows☆12Updated last year
- End-guided RNA assembler☆15Updated last month