WillJackson94's Stars
deepfakes/faceswap
Deepfakes Software For All
dmlc/xgboost
Scalable, Portable and Distributed Gradient Boosting (GBDT, GBRT or GBM) Library, for Python, R, Java, Scala, C++ and more. Runs on single machine, Hadoop, Spark, Dask, Flink and DataFlow
mnielsen/neural-networks-and-deep-learning
Code samples for my book "Neural Networks and Deep Learning"
google/deepvariant
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
PyTables/PyTables
A Python package to manage extremely large amounts of data
arq5x/bedtools2
bedtools - the swiss army knife for genome arithmetic
YuLab-SMU/ggtree
:christmas_tree:Visualization and annotation of phylogenetic trees
cBioPortal/cbioportal
cBioPortal for Cancer Genomics
KlugerLab/FIt-SNE
Fast Fourier Transform-accelerated Interpolation-based t-SNE (FIt-SNE)
Ensembl/ensembl-vep
The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants
seqan/seqan3
The modern C++ library for sequence analysis. Contains version 3 of the library and API docs.
Illumina/manta
Structural variant and indel caller for mapped sequencing data
jmzeng1314/tcga_example
kharchenkolab/pagoda2
R package for analyzing and interactively exploring large-scale single-cell RNA-seq datasets
Irrationone/cellassign
Automated, probabilistic assignment of cell types in scRNA-seq data
bioinform/neusomatic
NeuSomatic: Deep convolutional neural networks for accurate somatic mutation detection
griffithlab/pVACtools
broadinstitute/wot
A software package for analyzing snapshots of developmental processes
opencb/cellbase
High-Performance NoSQL database and RESTful web services to access to most relevant biological data. Found a bug or have an idea for a new feature? Let us know at https://zettagenomics.com/academic/
gatk-workflows/gatk4-somatic-snvs-indels
This repo has been archived, these workflows are still available in the GATK repository under the scripts directory. The workflows are also organized in Dockstore in the GATK Best Practices Workflows collection.
mskcc/mutation-signatures
Create mutation signatures from MAF's, and decompose them into Stratton signatures
whuJackie/ghelper
谷歌上网助手手动安装包
TRON-Bioinformatics/seq2HLA
In-silico method written in Python and R to determine HLA genotypes of a sample. seq2HLA takes standard RNA-Seq sequence reads in fastq format as input, uses a bowtie index comprising all HLA alleles and outputs the most likely HLA class I and class II genotypes (in 4 digit resolution), a p-value for each call, and the expression of each class.
felixfan/PyHLA
Python for HLA analysis: summary, association analysis, zygosity test and interaction test
jason-weirather/CIBERSORT
A shell to facilitate loading / running CIBERSORT software in structured environments
BaderLab/singleLiverCells
Scripts for processing single liver cells RNA-Seq 10X Genomics Data
mnielLab/netTCR
predicting peptide and TCR interaction
liyangbit/awesome-python-sources
include awesome python sources
linnarsson-lab/DG_paper_public
Matlab code
XuegongLab/HCA-reproducibility
A case study on the detailed reproducibility of a human cell atlas project