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Jupyter Notebook 1 Updated May 18, 2025

A quickstart tool for AmpliconArchitect. Performs all preliminary steps (alignment, CNV calling, seed interval detection) required prior to running AmpliconArchitect. Previously called PrepareAA.

Python 65 28 Updated May 15, 2025
Python 8 3 Updated Nov 22, 2024
Python 1 Updated Aug 18, 2022

Reconstruction of focal amplifications with long reads

Python 21 4 Updated May 16, 2025

Computing statistics for overlapping sets of intervals

C++ 6 2 Updated Aug 30, 2022

AWS for Bioinformatics Researchers

Jupyter Notebook 148 35 Updated Aug 22, 2024

SRA Tools

C 1,212 260 Updated May 20, 2025

GenePattern Python Library

Python 11 4 Updated Jan 26, 2024

A curated and opinionated list of resources for Chief Technology Officers, with the emphasis on startups

30,666 1,876 Updated May 13, 2025

fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

Nim 745 100 Updated Jan 17, 2025

Introduction to Computational Biology and Bioinformatics Course at Caltech, 2023

Jupyter Notebook 484 77 Updated Jan 5, 2024

Genomic coordinates of problematic genomic regions as GRanges

R 38 3 Updated Dec 9, 2024

Website to host AmpliconSuite outputs, including AA outputs and resulting focal amplification classifications, such as ecDNA.

JavaScript 4 5 Updated May 20, 2025

Aggregates the results from AmpliconSuite for upload to AmpliconRepository.org

Python 2 4 Updated Dec 5, 2024

Structural variation caller using third generation sequencing

Python 590 96 Updated Apr 14, 2025

Pull current and historical baseball statistics using Python (Statcast, Baseball Reference, FanGraphs)

Python 1,413 369 Updated Sep 24, 2024

Streamlit — A faster way to build and share data apps.

Python 39,421 3,454 Updated May 20, 2025

State-of-the-Art Deep Learning scripts organized by models - easy to train and deploy with reproducible accuracy and performance on enterprise-grade infrastructure.

Jupyter Notebook 14,265 3,334 Updated Aug 12, 2024

Wraps the AmpliconSuite-pipeline workflow to identify one or more connected genomic regions which have copy number amplifications.

Python 1 Updated May 9, 2025

Snakemake-based workflow for detecting structural variants in genomic data

Python 80 35 Updated Feb 14, 2025

Graphical Fragment Assembly (GFA) Format Specification

Makefile 207 44 Updated Aug 21, 2024

A flexible framework for nucleosome profiling of cell-free DNA

Python 8 5 Updated May 12, 2025

🧬 gget enables efficient querying of genomic reference databases

Python 1,024 77 Updated May 19, 2025
JavaScript 20 14 Updated Feb 21, 2025

Pipeline for the identification of extrachromosomal circular DNA (ecDNA) from Circle-seq, WGS, and ATAC-seq data that were generated from cancer and other eukaryotic cells.

Python 29 14 Updated Apr 30, 2025

Application for making ENCODE Blacklists

C++ 306 40 Updated Apr 23, 2021

Performant Pythonic GenomicRanges

Python 468 49 Updated Mar 14, 2025

Various algorithms for analysing genomics data

Java 224 59 Updated May 20, 2025

Toolset for SV simulation, comparison and filtering

C++ 377 48 Updated Dec 1, 2023
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