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  • Umeå University
  • Umeå
  • 17:46 (UTC +02:00)

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Software Release and Tutorials

6 Updated Apr 7, 2026

A fully-equipped, fast, memory-efficient pre-processor for ONT transcriptomic data

Python 2 2 Updated Feb 24, 2026

Cell type specific isoform estimator from bulk RNA-seq

R 4 Updated May 22, 2025

Improving gene isoform quantification with miniQuant

C++ 42 4 Updated Jan 13, 2026

Using long read RNAseq to catch the alternative Polyadenylation sites and monitor the lengthening or shortening trend of 3'UTRs

R 11 Updated May 15, 2026

A pipeline for differential expression and differential alternative splicing analysis

69 29 Updated Apr 26, 2024

PoGo is a proteogenomic tool which allows mapping of peptides identified through mass spectrometry to a reference genome through provided gene annotation.

C++ 12 9 Updated Jul 8, 2021

TX2P - Transcript to protein

R 5 Updated Nov 25, 2024

Assembler for multiple RNA-seq samples

C++ 9 1 Updated Apr 4, 2025
Python 9 Updated Oct 7, 2024
Python 2 1 Updated Apr 22, 2026

Refinement tool for transcript isoform identification using long reads.

Python 6 2 Updated Jul 18, 2025

FusionInspector code

Perl 61 23 Updated May 21, 2026

ChimPipe: Accurate detection of fusion genes and transcription-induced chimeras from RNA-seq data

Awk 15 11 Updated Jan 22, 2026

nextNEOpi: a comprehensive pipeline for computational neoantigen prediction

Nextflow 93 30 Updated Jun 6, 2025

"Dimensionality-increasing" data visualization tool and interactive WebGL Jupyter widget built for single-cell data.

HTML 120 20 Updated Dec 30, 2022

A tool for processing Split-seq reads to extract, correct, and tag barcodes, with statistical reports and visualizations.

Python 3 1 Updated Feb 24, 2026

tools for working with genome variation graphs

C++ 1,321 216 Updated Jun 19, 2026

Differential quantification of alternative splicing events on spliced pangenome graphs

Python 16 2 Updated Jan 30, 2026

GFHunter is a long read sequence transcriptome alignment-based fusion genes detection tool

Python 4 Updated Jun 8, 2026

Inclusive model of expression dynamics with conventional or metabolic labeling based scRNA-seq / multiomics, vector field reconstruction and differential geometry analyses

Python 502 60 Updated Apr 23, 2026

Single-Cell Omics for Transcriptome CHaracterization (SCOTCH): isoform-level characterization of gene expression through long-read single-cell RNA sequencing

Python 25 3 Updated Jun 1, 2026

DeepSAP repository for documentation and supplemental data

HTML 10 4 Updated Jun 10, 2026
Python 112 52 Updated Jan 23, 2026

Tool for IDentification and Enumeration of Spliced and Unspliced Read Fragments

Python 18 1 Updated Jun 14, 2026

single cell Cross- Annotation and Multimodal Estimation on Lineage trajectory

Jupyter Notebook 1 1 Updated Jun 10, 2026

trackplot is a tool for visualizing various next-generation sequencing (NGS) data, including DNA-seq, RNA-seq, single-cell RNA-seq and full-length sequencing datasets.

Python 104 12 Updated Jun 17, 2026

Comprehensive and scalable differential splicing analyses

C 18 4 Updated Dec 19, 2025

Nextflow pipeline for performing parallel alternative splicing analysis using rMATS and Whippet and then overlapping the results.

Nextflow 9 5 Updated Dec 5, 2022

splicekit: an integrative toolkit for splicing analysis from short-read RNA-seq

Python 23 4 Updated Nov 28, 2025
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