meissnert

meissnert's Stars

• nvbn/thefuck

  Magnificent app which corrects your previous console command.

  Language:Python89.1k8357403.6k

• DataTalksClub/data-engineering-zoomcamp

  Free Data Engineering course!

  Language:Jupyter Notebook27.3k4981295.7k

• ossu/data-science

  📊 Path to a free self-taught education in Data Science!

  19.3k972583.5k

• overleaf/overleaf

  A web-based collaborative LaTeX editor

  Language:JavaScript14.6k2111.1k1.5k

• DataTalksClub/machine-learning-zoomcamp

  Learn ML engineering for free in 4 months!

  Language:Jupyter Notebook9.8k1641572.3k

• pditommaso/awesome-pipeline

  A curated list of awesome pipeline toolkits inspired by Awesome Sysadmin

  6.2k23027628

• alexdobin/STAR

  RNA-seq aligner

  Language:C1.9k792.1k513

• ramnathv/rCharts

  Interactive JS Charts from R

  Language:JavaScript1.2k133683654

• aws/aws-parallelcluster

  AWS ParallelCluster is an AWS supported Open Source cluster management tool to deploy and manage HPC clusters in the AWS cloud.

  Language:Python851871.2k312

• jtriley/StarCluster

  StarCluster is an open source cluster-computing toolkit for Amazon's Elastic Compute Cloud (EC2).

  Language:Python58165447308

• dellytools/delly

  DELLY2: Structural variant discovery by integrated paired-end and split-read analysis

  Language:C++45434367138

• rasmusab/bayesian_first_aid

  Inside every classical test there is a Bayesian model trying to get out.

  Language:R326562340

• seandavi/awesome-cancer-variant-databases

  A community-maintained repository of cancer clinical knowledge bases and databases focused on cancer variants.

  30033269

• ExaScience/elprep

  elPrep: a high-performance tool for analyzing sequence alignment/map files in sequencing pipelines.

  Language:Go288196440

• jimhester/knitrBootstrap

  A framework to create bootstrap styled HTML reports from knitr Rmarkdown.

  Language:HTML274288861

• sigven/pcgr

  Personal Cancer Genome Reporter (PCGR)

  Language:R2562415048

• WGLab/InterVar

  A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline

  Language:Python190319893

• genome/sciclone

  An R package for inferring the subclonal architecture of tumors

  Language:R117485155

• biothings/myvariant.info

  MyVariant.info: A BioThings API for human variant annotations

  Language:Python883013532

• tiagoboldt/sharelatex-docker

  Sharelatex instalation via Dockerfile

  Language:CoffeeScript748031

• PhanstielLab/Sushi

  Tools for visualizing genomics data

  Language:R67122020

• srp33/TCGA_RNASeq_Clinical

  Language:HTML6013140

• wrathematics/Rfiglet

  R bindings for figlet

  Language:C15204

• carlandt/ngs-slider

  My homebrew pipelines for taking next-gen sequencing data and finding decent variants!

  Language:Shell6241

• JaegyoonAhn/RASER

  630

• cband/MOJO

  Language:C++5321