jluebeck
Bioinformatics post-doc at UC San Diego working in the Vineet Bafna lab. Lead developer of @AmpliconSuite.
UC San DiegoSan Diego
jluebeck's Stars
chrislgarry/Apollo-11
Original Apollo 11 Guidance Computer (AGC) source code for the command and lunar modules.
streamlit/streamlit
Streamlit — A faster way to build and share data apps.
NVIDIA/DeepLearningExamples
State-of-the-Art Deep Learning scripts organized by models - easy to train and deploy with reproducible accuracy and performance on enterprise-grade infrastructure.
academicpages/academicpages.github.io
Github Pages template for academic personal websites, forked from mmistakes/minimal-mistakes
jldbc/pybaseball
Pull current and historical baseball statistics using Python (Statcast, Baseball Reference, FanGraphs)
pachterlab/gget
🧬 gget enables efficient querying of genomic reference databases
marbl/CHM13
The complete sequence of a human genome
mikelove/awesome-multi-omics
List of software packages for multi-omics analysis
fritzsedlazeck/Sniffles
Structural variation caller using third generation sequencing
etal/cnvkit
Copy number variant detection from targeted DNA sequencing
pyranges/pyranges
Performant Pythonic GenomicRanges
pachterlab/BI-BE-CS-183-2023
Introduction to Computational Biology and Bioinformatics Course at Caltech, 2023
fritzsedlazeck/SURVIVOR
Toolset for SV simulation, comparison and filtering
Boyle-Lab/Blacklist
Application for making ENCODE Blacklists
GFA-spec/GFA-spec
Graphical Fragment Assembly (GFA) Format Specification
hartwigmedical/hmftools
Various algorithms for analysing genomics data
lh3/cgranges
A C/C++ library for fast interval overlap queries (with a "bedtools coverage" example)
virajbdeshpande/AmpliconArchitect
AmpliconArchitect (AA) is a tool to identify one or more connected genomic regions which have simultaneous copy number amplification and elucidates the architecture of the amplicon. In the current version, AA takes as input next generation sequencing reads (paired-end Illumina reads) mapped to the hg19/GRCh37 reference sequence and one or more regions of interest. Please "watch" this repository for improvements in runtime, accuracy and annotations for GRCh38 human reference genome coming up soon.
GooglingTheCancerGenome/sv-callers
Snakemake-based workflow for detecting structural variants in genomic data
namphuon/ViFi
Pipeline for identifying viral integration and fusion mRNA reads from NGS data. Manuscript is currently in preparation.
nf-core/circdna
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.
dozmorovlab/excluderanges
Genomic coordinates of problematic genomic regions as GRanges
FadyMohareb/mapoptics
MapOptics is a lightweight cross-platform tool that enables the user to visualise and interact with the alignment of Bionano optical mapping data and can be used for in depth exploration of hybrid scaffolding alignments.
chezbob/chezbob
sara-javadzadeh/FastViFi
Detect viral infection and integration sites on NGS input. Manuscript is in preparation.
GavinHaLab/Griffin
A flexible framework for nucleosome profiling of cell-free DNA
AmpliconSuite/AmpliconSuiteAggregator
Aggregates the results from AmpliconSuite for upload to AmpliconRepository.org
AmpliconSuite/AmpliconRepository
Website to host AmpliconSuite outputs, including AA outputs and resulting focal amplification classifications, such as ecDNA.
genepattern/AmpliconSuite
Wraps the AmpliconSuite-pipeline workflow to identify one or more connected genomic regions which have copy number amplifications.