On the public citation graph

Machine learning models to predict in vivo drug response via optimal dimensionality reduction of tumour molecular profiles

0 signed · 66 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-3-319-55825-7_9openalex-snapshot
Using PDX for Biomarker Development
inferredcites →https://doi.org/10.1016/0005-2795(75)90109-9openalex-snapshot
Comparison of the predicted and observed secondary structure of T4 phage lysozyme
inferredcites →https://doi.org/10.1016/j.cell.2016.08.041openalex-snapshot
A Biobank of Breast Cancer Explants with Preserved Intra-tumor Heterogeneity to Screen Anticancer Compounds
inferredcites →https://doi.org/10.1016/j.celrep.2017.10.021openalex-snapshot
A Comprehensive Patient-Derived Xenograft Collection Representing the Heterogeneity of Melanoma
inferredcites →https://doi.org/10.1016/j.drudis.2012.12.011openalex-snapshot
Challenges and opportunities for oncology biomarker discovery
inferredcites →https://doi.org/10.1016/j.tips.2013.11.004openalex-snapshot
Molecularly targeted cancer therapy: some lessons from the past decade
inferredcites →https://doi.org/10.1016/j.ygeno.2012.04.003openalex-snapshot
Random forests for genomic data analysis
inferredcites →https://doi.org/10.1016/s1471-4914(01)01986-4openalex-snapshot
Clinical application of pharmacogenetics
inferredcites →https://doi.org/10.1021/ci034160gopenalex-snapshot
Random Forest: A Classification and Regression Tool for Compound Classification and QSAR Modeling
inferredcites →https://doi.org/10.1021/ci400573copenalex-snapshot
Choosing Feature Selection and Learning Algorithms in QSAR
inferredcites →https://doi.org/10.1023/a:1010933404324openalex-snapshot
Random Forests
inferredcites →https://doi.org/10.1023/a:1012487302797openalex-snapshot
Gene Selection for Cancer Classification using Support Vector Machines
inferredcites →https://doi.org/10.1038/537s63aopenalex-snapshot
Perspective: The precision-oncology illusion
inferredcites →https://doi.org/10.1038/nature10868openalex-snapshot
Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR
inferredcites →https://doi.org/10.1038/nature11003openalex-snapshot
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
inferredcites →https://doi.org/10.1038/nature11005openalex-snapshot
Systematic identification of genomic markers of drug sensitivity in cancer cells
inferredcites →https://doi.org/10.1038/nature23647openalex-snapshot
Orthotopic patient-derived xenografts of paediatric solid tumours
inferredcites →https://doi.org/10.1038/nbt.2877openalex-snapshot
A community effort to assess and improve drug sensitivity prediction algorithms
inferredcites →https://doi.org/10.1038/nchembio.1986openalex-snapshot
Correlating chemical sensitivity and basal gene expression reveals mechanism of action
inferredcites →https://doi.org/10.1038/ncomms3126openalex-snapshot
Evaluating cell lines as tumour models by comparison of genomic profiles
inferredcites →https://doi.org/10.1038/nm.3954openalex-snapshot
High-throughput screening using patient-derived tumor xenografts to predict clinical trial drug response
inferredcites →https://doi.org/10.1038/nrc2294openalex-snapshot
The properties of high-dimensional data spaces: implications for exploring gene and protein expression data
inferredcites →https://doi.org/10.1038/nrg3920openalex-snapshot
Machine learning applications in genetics and genomics
inferredcites →https://doi.org/10.1056/nejmoa050736openalex-snapshot
Erlotinib in Lung Cancer — Molecular and Clinical Predictors of Outcome
inferredcites →https://doi.org/10.1056/nejmoa1112302openalex-snapshot
Survival in BRAF V600–Mutant Advanced Melanoma Treated with Vemurafenib
inferredcites →https://doi.org/10.1093/annonc/mds309openalex-snapshot
Can sensitivity to cytotoxic chemotherapy be predicted by biomarkers?
inferredcites →https://doi.org/10.1093/annonc/mdx416openalex-snapshot
Patient-derived xenografts effectively capture responses to oncology therapy in a heterogeneous cohort of patients with solid tumors
inferredcites →https://doi.org/10.1093/bioinformatics/btm344openalex-snapshot
A review of feature selection techniques in bioinformatics
inferredcites →https://doi.org/10.1093/bioinformatics/btq112openalex-snapshot
A machine learning approach to predicting protein–ligand binding affinity with applications to molecular docking
inferredcites →https://doi.org/10.1093/bioinformatics/btv529openalex-snapshot
Improved large-scale prediction of growth inhibition patterns using the NCI60 cancer cell line panel
inferredcites →https://doi.org/10.1093/bioinformatics/btx266openalex-snapshot
Systematic identification of feature combinations for predicting drug response with Bayesian multi-view multi-task linear regression
inferredcites →https://doi.org/10.1093/jnci/djv247openalex-snapshot
Predicting Response to Histone Deacetylase Inhibitors Using High-Throughput Genomics
inferredcites →https://doi.org/10.1093/nar/gks1111openalex-snapshot
Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells
inferredcites →https://doi.org/10.1109/tcbb.2014.2321138openalex-snapshot
An Integrated Approach to Anti-Cancer Drug Sensitivity Prediction
inferredcites →https://doi.org/10.1111/joim.12321openalex-snapshot
Pharmacogenomic biomarkers for personalized cancer treatment
inferredcites →https://doi.org/10.1155/2015/198363openalex-snapshot
A Review of Feature Selection and Feature Extraction Methods Applied on Microarray Data
inferredcites →https://doi.org/10.1158/1078-0432.ccr-12-2408openalex-snapshot
The Promise of Patient-Derived Xenografts: The Best Laid Plans of Mice and Men
inferredcites →https://doi.org/10.1158/1078-0432.ccr-15-2401openalex-snapshot
Comparing Patient-Derived Xenograft and Computational Response Prediction for Targeted Therapy in Patients of Early-Stage Large Cell Lung Cancer
inferredcites →https://doi.org/10.1158/1541-7786.mcr-15-0189openalex-snapshot
Tumor-Derived Cell Lines as Molecular Models of Cancer Pharmacogenomics
inferredcites →https://doi.org/10.1158/1541-7786.mcr-17-0378openalex-snapshot
Precision Oncology beyond Targeted Therapy: Combining Omics Data with Machine Learning Matches the Majority of Cancer Cells to Effective Therapeutics
inferredcites →https://doi.org/10.1158/2159-8290.cd-14-0001openalex-snapshot
Patient-Derived Xenograft Models: An Emerging Platform for Translational Cancer Research
inferredcites →https://doi.org/10.1158/2159-8290.cd-17-0151openalex-snapshot
AACR Project GENIE: Powering Precision Medicine through an International Consortium
inferredcites →https://doi.org/10.1186/1471-2105-7-91openalex-snapshot
Bias in error estimation when using cross-validation for model selection
inferredcites →https://doi.org/10.1186/gb-2014-15-3-r47openalex-snapshot
Clinical drug response can be predicted using baseline gene expression levels and in vitro drug sensitivity in cell lines
inferredcites →https://doi.org/10.1186/s12885-015-1237-6openalex-snapshot
Predicting response to multidrug regimens in cancer patients using cell line experiments and regularised regression models
inferredcites →https://doi.org/10.1186/s12920-018-0336-zopenalex-snapshot
Unearthing new genomic markers of drug response by improved measurement of discriminative power
inferredcites →https://doi.org/10.1186/s13058-015-0613-0openalex-snapshot
Assessing breast cancer cell lines as tumour models by comparison of mRNA expression profiles
inferredcites →https://doi.org/10.1200/jco.2013.49.8691openalex-snapshot
Phase II Trial (BREAK-2) of the BRAF Inhibitor Dabrafenib (GSK2118436) in Patients With Metastatic Melanoma
inferredcites →https://doi.org/10.12688/f1000research.10529.1openalex-snapshot
Systematic assessment of multi-gene predictors of pan-cancer cell line sensitivity to drugs exploiting gene expression data
inferredcites →https://doi.org/10.12688/f1000research.10529.2openalex-snapshot
Systematic assessment of multi-gene predictors of pan-cancer cell line sensitivity to drugs exploiting gene expression data
inferredcites →https://doi.org/10.1371/journal.pone.0028210openalex-snapshot
The Influence of Feature Selection Methods on Accuracy, Stability and Interpretability of Molecular Signatures
inferredcites →https://doi.org/10.1371/journal.pone.0061318openalex-snapshot
Machine Learning Prediction of Cancer Cell Sensitivity to Drugs Based on Genomic and Chemical Properties
inferredcites →https://doi.org/10.1371/journal.pone.0120408openalex-snapshot
DISIS: Prediction of Drug Response through an Iterative Sure Independence Screening
inferredcites →https://doi.org/10.1371/journal.pone.0127433openalex-snapshot
Data Mining Approaches for Genomic Biomarker Development: Applications Using Drug Screening Data from the Cancer Genome Project and the Cancer Cell Line Encyclopedia
inferredcites →https://doi.org/10.14348/molcells.2016.2350openalex-snapshot
An Integrative Approach to Precision Cancer Medicine Using Patient-Derived Xenografts
inferredcites →https://doi.org/10.18632/oncotarget.20923openalex-snapshot
Precision and recall oncology: combining multiple gene mutations for improved identification of drug-sensitive tumours
inferredcites →https://doi.org/10.18632/oncotarget.7012openalex-snapshot
Identifying anti-cancer drug response related genes using an integrative analysis of transcriptomic and genomic variations with cell line-based drug perturbations
inferredcites →https://doi.org/10.3390/ijms16010747openalex-snapshot
Gene Mutation Analysis in EGFR Wild Type NSCLC Responsive to Erlotinib: Are There Features to Guide Patient Selection?
inferredcites →https://doi.org/10.5555/1756006.1859921openalex-snapshot
On Over-fitting in Model Selection and Subsequent Selection Bias in Performance Evaluation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1038/s41598-019-50720-0openalex-snapshot
Modeling cancer drug response through drug-specific informative genes
inferred← citeshttps://doi.org/10.1093/bib/bbab312openalex-snapshot
A gentle introduction to understanding preclinical data for cancer pharmaco-omic modeling
inferred← citeshttps://doi.org/10.1186/s12885-024-12575-1openalex-snapshot
Investigating the effects of artificial intelligence on the personalization of breast cancer management: a systematic study
inferred← citeshttps://doi.org/10.1186/s13321-020-00444-5openalex-snapshot
QSAR-derived affinity fingerprints (part 2): modeling performance for potency prediction
inferred← citeshttps://doi.org/10.3389/fgene.2019.01041openalex-snapshot
Paclitaxel Response Can Be Predicted With Interpretable Multi-Variate Classifiers Exploiting DNA-Methylation and miRNA Data
inferred← citeshttps://doi.org/10.3390/biom10060963openalex-snapshot
Concise Polygenic Models for Cancer-Specific Identification of Drug-Sensitive Tumors from Their Multi-Omics Profiles
inferred← citeshttps://doi.org/10.70675/df2ce30ez1a6bz4ba3z9798z284f80a7fa8dopenalex-snapshot
Prediction of tumour in vivo response to treatments using its molecular profiles via machine learning
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.