novapyth's Stars
anergictcell/pyhpo
A Python library to work with, analyze, filter and inspect the Human Phenotype Ontology
IARCbioinfo/IARC-nf
List of IARC bioinformatics nextflow pipelines
ANGSD/NgsRelate
basir/next-amazona
AstraZeneca-NGS/VarDict
VarDict
J35P312/SVDB
structural variant database software
labsquare/cutevariant
A standalone and free application to explore genetics variations from VCF file
Steven-N-Hart/vcf-miner
VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files
babelomics/bierapp
This interactive tool allows finding genes affected by deleterious variants that segregate along family pedigrees , case-controls or sporadic samples
freeCodeCamp/freeCodeCamp
freeCodeCamp.org's open-source codebase and curriculum. Learn to code for free.
novapyth/readme
satijalab/seurat
R toolkit for single cell genomics
gersteinlab/aloft
ALOFT, the Annotation Of Loss-of-Function Transcripts, provides extensive functional annotations to loss-of-function variants in the human genome.
novapyth/Nucleocapsid-N-Protein-of-SARS-CoV-2
luksa/kubernetes-in-action-2nd-edition
Code from the Kubernetes in Action 2nd Edition book
novapyth/Publications-year-wise
Publication
rstudio/rmarkdown-book
R Markdown: The Definitive Guide (published by Chapman & Hall/CRC in July 2018)
datacarpentry/R-genomics
Lesson on data analysis and visualization in R for genomics
hail-is/hail
Cloud-native genomic dataframes and batch computing
novapyth/ICDSB2020
ICDSB2020 - International Conference on Data Science in Biology 2020
novapyth/Scopulariopsis_brevicaulis
novapyth/MARINEFUNGI
novapyth/Learn_R_and_Use_R
Learn R and Use R
novapyth/International_Webinar_COVID19
International Webinar on COVID-19 pandemic at Institute of Bioinformatics, Bangalore, India