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Dec 7, 2020 - Python
#
cancer
Here are 417 public repositories matching this topic...
Code for the Nature Scientific Reports paper "Pathologist-level classification of histologic patterns on resected lung adenocarcinoma slides with deep neural networks." A sliding window framework for classification of high resolution whole-slide images, often microscopy or histopathology images.
cancer
resnet
microscopy
sliding-windows
lung
wsi
medical-image-analysis
pathology-image
histopathology-images
Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
bioinformatics
snps
medicine
genomics
genome
cancer
biology
vcf
ensembl
medical
cancer-genomics
genome-annotation
proteomics
gtf
bed
cancer-genomes
genome-sequencing
genome-browser
genomes
csv-parser
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Sep 21, 2020 - Python
A community-maintained repository of cancer clinical knowledge bases and databases focused on cancer variants.
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Mar 13, 2019
Personal Cancer Genome Reporter (PCGR)
interpreter
cancer
clinical
tumor
vcf
cancer-genomics
reporting-engine
copy-number-variation
annotation-tool
somatic
cancer-variants
annotation-framework
snvs
oncology-data
precision-oncology
variant-interpretation
therapeutic-targets
precision-cancer-medicine
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Jan 25, 2021 - R
Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
docker
workflow
bioinformatics
pipeline
genomics
nextflow
cancer
somatic-variants
reproducible-research
containers
next-generation-sequencing
singularity
badge
reproducible-science
travis-link
somatic
germline
scilifelab
gitter-badge
germline-variants
gitter-link
scilifelab-link
nextflow-link
nbis-link
ngi-link
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Jan 27, 2020 - Nextflow
Training and evaluating a variational autoencoder for pan-cancer gene expression data
deep-learning
analysis
script
tool
cancer
gene-expression
cancer-genomics
autoencoder
unsupervised-learning
variational-autoencoder
variational-autoencoders
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Jan 31, 2019 - HTML
Detect and visualize target mutations by scanning FastQ files directly
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Jan 21, 2020 - C
Cancer Imaging Phenomics Toolkit (CaPTk) is a software platform to perform image analysis and predictive modeling tasks. Documentation: https://cbica.github.io/CaPTk/
machine-learning
analytics
cpp
cancer
cpp11
medical-imaging
cancer-imaging-research
image-analysis
medical-image-computing
cwl
itcr
radiomics
medical-image-processing
nih
nci
nci-itcr
radiomics-features
cwltool
u24
cbica
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Jan 30, 2021 - C++
Putting machine learning in the hands of cancer biologists
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Oct 27, 2017 - Jupyter Notebook
Fast and accurate gene fusion detection from RNA-Seq data
rna-seq
cancer
gene-fusion
star
variant-calling
virus-integration
structural-variation
fusion-genes
gene-fusions
fusion-gene
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Mar 2, 2021 - C++
Building classifiers using cancer transcriptomes across 33 different cancer-types
classifier
machine-learning
analysis
tool
cancer
tcga
gene-expression
methodology
transcriptome
pancancer
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Apr 30, 2019 - Jupyter Notebook
A collection of small-sample, high-dimensional microarray data sets to assess machine-learning algorithms and models.
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Jan 10, 2016 - R
A Slicer extension to provide a GUI around pyradiomics
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Nov 9, 2020 - Python
Provide R access to the NCI Genomic Data Commons portal.
data-science
bioinformatics
r
genomics
cancer
tcga
api-client
core-services
bioconductor
vignette
nci
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Oct 27, 2020 - R
Web client for CIViC: Clinical Interpretations of Variants in Cancer
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Mar 9, 2021 - JavaScript
This project is all about a Machine Learning based Medical Test web app which makes predictions about various diseases using the concept of machine learning.
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Nov 13, 2020 - HTML
Classifies genes as an oncogene, tumor suppressor gene, or as a non-driver gene by using Random Forests
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Sep 7, 2020 - Python
A list of web-based interactive biological data visualizations.
visualization
awesome
medicine
genomics
cancer
biology
data-visualization
awesome-list
transcriptomics
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Feb 26, 2021
An interactive web portal for exploring immuno-oncology data
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Feb 26, 2021 - R
Python package to annotate and visualize gene fusions.
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Nov 9, 2019 - Python
Backend Server for CIViC Project
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Mar 11, 2021 - HTML
3D hotspot mutation proximity analysis tool
analysis
cancer
clustering
perl
protein-structure
ensembl
mutations
pymol
hgnc
disease
drug
drugbank
hotspot
uniprot
blat
3d-proximity
proximity-search
genomic
drugport
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Aug 22, 2019 - Perl
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Aug 25, 2020 - HTML
Text-mined knowledgebase for drivers, oncogenes and tumor suppressors in cancer
text-mining
cancer
precision-medicine
bionlp
oncogenes
tumor-suppressors
cancer-driver-genes
cancer-types
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Dec 2, 2020 - R
1
noobkid2411
commented
Mar 11, 2021
This seems to be a relevant sub project for this project. I would like to work on it.
Here is the source of the dataset I will use:
https://www.sciencedirect.com/science/article/pii/S2352340920300081?via%3Dihub
I am a GSSOC'21 Participant.
MATLAB implementation to segment breast lesions in ultrasound images (ICIAR 2016)
computer-vision
cancer
paper
matlab
image-processing
medical-imaging
segmentation
ultrasound
normalized-cuts
segementation
quickshift
ultrasound-images
segment-breast-lesions
bus-segmentation
automatic-nonlinear-filtering
gerard-pons
mohamed
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Oct 12, 2019 - MATLAB
A Python-Tensorflow neural network for classifying cancer data
python
deep-learning
cancer
tensorflow
recurrent-neural-networks
convolutional-neural-networks
neural-nets
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Jun 27, 2017 - Python
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It would be nice to add a params to choose the VEP genome assembly.
In most cases it is the
--genomeparams, but I'm assuming it'll be easier to control if we have that as a separate params.For example, it's currently not working with the
--genome customsetting.