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  • License
    Apache License 2.0
  • Created 5 months ago
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Repository Details

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1

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4

awesome-drug-discovery-knowledge-graphs

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Readings for "A Unified View of Relational Deep Learning for Drug Pair Scoring." (IJCAI 2022)
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11

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12

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13

kallisto

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14

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15

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16

kgem-in-drug-discovery

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17

StarGazer

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18

Omicsfold

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19

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20

peptide-tools

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21

data-science-python-course

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22

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A plugin to read whole slide images within napari.
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23

biomedical-kg-topological-imbalance

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24

ibd-interpret

We trained high performing open source models on image scans of tissue biopsies to predict endoscopic categories in inflammatory bowel disease. These predictive models can help us better understand the disease pathology and represent a step towards automated clinical recruitment strategies.
Python
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25

roo

A package and environment manager for R
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26

NESS

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27

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28

skywalkR-graph-features

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29

multimodal-python-course

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30

UnlockingHeart

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31

Tendril

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32

CTELC-Patient-Attrition-Model

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33

MVDA_exploration_tools

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34

Siamese-Regression-Pairing

Siamese Neural Networks for Regression: Similarity-Based Pairing and Uncertainty Quantification
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35

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36

hsqc_structure_elucidation

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Multimodal_NSCLC

multi-omics data integration helps improving patient survival prediction. We provide a pipeline allowing for early integration of multiple omics plus clinical modalities in order to predict patient survival for NSCLC. The pipeline utilizes autoencoders, and helps identify main driving factor in survival prediction
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38

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Extensions packages for magnus
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39

fragler

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40

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41

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43

MCPL

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44

qscheck

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45

molecular-complexity

Python implementation of the molecular complexity metric described by Proudfoot 2017 (http://dx.doi.org/10.1016/j.bmcl.2017.03.008).
Python
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46

Machine-Learning-for-Predicting-Targeted-Protein-Degradation

The code was developed for training diverse ML and DL models to predict PROTACs degradation. Data cleaning for two public datasets, PROTAC-DB and PROTACpedia, are also included. PROTACs are of high interest for all disease areas of AZ and thus predicting their degradation is of general interest.
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47

OSPred

The OSPred tool offers interactive visualization of clinical trial end point correlations with reference to a large pool of historical NSCLC studies. Its focused capability has the potential to digitally transform and accelerate data-driven decision making as part of the drug development process. OSPred enables data scientists to rapidly visualize, analyze and validate the endpoint (PFS, ORR, OS) correlation hypothesis and to predict HR OS, which potentially could lead to faster and cost-effective NSCLC clinical trials. OSPred - A Digital Health Aid for Rapid Analysis of Early Endpoints (PFS, ORR) In clinical trials that assess novel therapeutic agents in patients with non-small-cell lung cancer (NSCLC), early endpoints (e.g. progression-free survival [PFS] and objective response rate) are often evaluated as indicators of biological drug activity, and are used as surrogate endpoints for overall survival (OS). A data set was compiled to investigate ascertain correlation trends between early endpoints (e.g. odds ratio [OR] for PFS at 6 months) and late endpoints (e.g. hazard ratio [HR] OS). The dataset was curated from multiple source databases, including ClinicalTrials.gov, PubMed and Citeline(TrialTrove). We applied a random-effects method for meta-analysis of prior RCT data to correlate a variety of estimates with the hazard ratio (HR) for OS and PFS. We performed meta-regression analyses across different data-strata, stratified by the mechanism of action as PD1/PDL1, EGFR, VEGFR, DNA and evaluated the correlation of trial-level, treatment effects between early (e.g. PFS) and late (e.g. OS) endpoints in NSCLC oncology trials.
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48

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49

survextrap-excesshazards

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50

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51

trim21-bioprotac

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52

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53

multitask_impute

Supplementary code for 'Deep Learning Imputation for Multi Task Learning'
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