VictorGoitea's Stars
prokischlab/omicsDiagnostics
This repository contains different scripts to automate and visualize analysis performed for the "Integration of proteomics with genomics and transcriptomics increases the diagnosis rate of Mendelian disorders"
ENCODE-DCC/kentUtils
UCSC command line bioinformatic utilities
liguowang/CrossMap
CrossMap is a python program to lift over genome coordinates from one genome version to another.
jernst98/ChromHMM
samtools/bcftools
This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html
mikelove/awesome-multi-omics
List of software packages for multi-omics analysis
broadinstitute/AwesomeGenomics
Cancer Data Science's go to place for excellent genomics tools and packages
broadinstitute/2019_scWorkshop
Repo for Physalia course Analysis of Single Cell RNA-Seq data
broadinstitute/gtex-pipeline
GTEx & TOPMed data production and analysis pipelines
broadinstitute/pilon
Pilon is an automated genome assembly improvement and variant detection tool
broadinstitute/infercnv
Inferring CNV from Single-Cell RNA-Seq
broadinstitute/picard
A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
broadinstitute/TAG-public
Official workflows published by the Broad Institute's Genomics Platform Translation Analysis Group (TAG)
broadinstitute/depmap_omics
What you need to process the Quarterly DepMap-Omics releases from Terra
broadinstitute/gatk
Official code repository for GATK versions 4 and up
broadinstitute/str-analysis
Scripts and utilities related to analyzing short tandem repeats (STRs).
dougspeed/LDAK
fizwit/easy_update
Update EasyBuild package configuration files for R and Python bundles
hds-sandbox/NGS_summer_course_Aarhus
Repository for the NGS summer course at Aarhus university
kundajelab/phantompeakqualtools
This package computes informative enrichment and quality measures for ChIP-seq/DNase-seq/FAIRE-seq/MNase-seq data. It can also be used to obtain robust estimates of the predominant fragment length or characteristic tag shift values in these assays.
jokergoo/simplifyEnrichment
Simplify functional enrichment results
YuLab-SMU/clusterProfiler
:bar_chart: A universal enrichment tool for interpreting omics data
YuLab-SMU/DOSE
:mask: Disease Ontology Semantic and Enrichment analysis
YuLab-SMU/ReactomePA
Reactome Pathway Analysis
YuLab-SMU/GOSemSim
:golf: GO-terms Semantic Similarity Measures
YuLab-SMU/meshes
:stethoscope: MeSH Enrichment and Semantic analyses
YuLab-SMU/ChIPseeker
:dart: ChIP peak Annotation, Comparison and Visualization
jokergoo/rGREAT
GREAT Analysis - Functional Enrichment on Genomic Regions
igvteam/igv
Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations
readthedocs-examples/awesome-read-the-docs
A curated list of awesome Read the Docs projects