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Author Details
Full Name
Suleyman Cenk Sahinalp
Affiliation
National Cancer Institute, National Institutes of Health
ORCID
Career Start Year
2001
Papers
105
H Index
39
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36657977
An efficient genotyper and star-allele caller for pharmacogenomics.
Genome Res
2023
37316351
Single-cell methylation sequencing data reveal succinct metastatic migration histories and tumor progression models.
Genome Res
2023
37469403
Computational pharmacogenotype extraction from clinical next-generation sequencing.
Front Oncol
2023
37333132
Melanoma clonal subline analysis uncovers heterogeneity-driven immunotherapy resistance mechanisms.
bioRxiv
2023
35134542
CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project.
J Mol Diagn
2022
35452844
Analytical Validation of a Computational Method for Pharmacogenetic Genotyping from Clinical Whole Exome Sequencing.
J Mol Diagn
2022
36307411
Strain level microbial detection and quantification with applications to single cell metagenomics.
Nat Commun
2022
36064595
Big data in basic and translational cancer research.
Nat Rev Cancer
2022
36265467
ImmunoTyper-SR: A computational approach for genotyping immunoglobulin heavy chain variable genes using short-read data.
Cell Syst
2022
35132409
ImmunoTyper-SR: A Novel Computational Approach for Genotyping Immunoglobulin Heavy Chain Variable Genes using Short Read Data.
bioRxiv
2022
34297621
Studying the History of Tumor Evolution from Single-Cell Sequencing Data by Exploring the Space of Binary Matrices.
J Comput Biol
2021
34859247
Privacy-Preserving Genotype Imputation in a Trusted Execution Environment.
Res Comput Mol Biol
2021
34391887
Proteogenomic Analysis Unveils the HLA Class I-Presented Immunopeptidome in Melanoma and EGFR-Mutant Lung Adenocarcinoma.
Mol Cell Proteomics
2021
34450045
Privacy-preserving genotype imputation in a trusted execution environment.
Cell Syst
2021
32160033
PyGTED: Python Application for Computing Graph Traversal Edit Distance.
J Comput Biol
2020
32058803
Graph Traversal Edit Distance and Extensions.
J Comput Biol
2020
32657374
Identification of conserved evolutionary trajectories in tumors.
Bioinformatics
2020
32896768
Erratum: Genotyping and Copy Number Analysis of Immunoglobulin Heavy Chain Variable Genes Using Long Reads.
iScience
2020
32132732
Sketching algorithms for genomic data analysis and querying in a secure enclave.
Nat Methods
2020
32483558
Clonal Evolution and Heterogeneity of Osimertinib Acquired Resistance Mechanisms in EGFR Mutant Lung Cancer.
Cell Rep Med
2020
30561550
lordFAST: sensitive and Fast Alignment Search Tool for LOng noisy Read sequencing Data.
Bioinformatics
2019
31372179
A multi-labeled tree dissimilarity measure for comparing "clonal trees" of tumor progression.
Algorithms Mol Biol
2019
30735634
Widespread and Functional RNA Circularization in Localized Prostate Cancer.
Cell
2019
30889379
The Proteogenomic Landscape of Curable Prostate Cancer.
Cancer Cell
2019
30963078
Protecting Genomic Data Privacy with Probabilistic Modeling.
Pac Symp Biocomput
2019
29267878
Computational identification of micro-structural variations and their proteogenomic consequences in cancer.
Bioinformatics
2018
29808028
Analysis of the androgen receptor-regulated lncRNA landscape identifies a role for ARLNC1 in prostate cancer progression.
Nat Genet
2018
30011248
Preface: Selected Articles from RECOMB 2017.
J Comput Biol
2018
28330676
Stromal Gene Expression is Predictive for Metastatic Primary Prostate Cancer.
Eur Urol
2018
29617966
MechRNA: prediction of lncRNA mechanisms from RNA-RNA and RNA-protein interactions.
Bioinformatics
2018
29422526
Optimal compressed representation of high throughput sequence data via light assembly.
Nat Commun
2018
29700301
Publisher Correction: Optimal compressed representation of high throughput sequence data via light assembly.
Nat Commun
2018
29483503
Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes.
Nat Commun
2018
29757368
The long noncoding RNA landscape of neuroendocrine prostate cancer and its clinical implications.
Gigascience
2018
27180064
SRRM4 Drives Neuroendocrine Transdifferentiation of Prostate Adenocarcinoma Under Androgen Receptor Pathway Inhibition.
Eur Urol
2017
28985744
Correction to: ReMixT: clone-specific genomic structure estimation in cancer.
Genome Biol
2017
28954787
Mutational Analysis of Gene Fusions Predicts Novel MHC Class I-Restricted T-Cell Epitopes and Immune Signatures in a Subset of Prostate Cancer.
Clin Cancer Res
2017
28750660
ReMixT: clone-specific genomic structure estimation in cancer.
Genome Biol
2017
28768687
HIT'nDRIVE: patient-specific multidriver gene prioritization for precision oncology.
Genome Res
2017
28786365
PRESAGE: PRivacy-preserving gEnetic testing via SoftwAre Guard Extension.
BMC Med Genomics
2017
28056180
Clonality Inference from Single Tumor Samples Using Low-Coverage Sequence Data.
J Comput Biol
2017
28068672
Genomic hallmarks of localized, non-indolent prostate cancer.
Nature
2017
28065902
PRINCESS: Privacy-protecting Rare disease International Network Collaboration via Encryption through Software guard extensionS.
Bioinformatics
2017
27531099
SiNVICT: ultra-sensitive detection of single nucleotide variants and indels in circulating tumour DNA.
Bioinformatics
2017
27453444
Enabling Privacy-Preserving GWASs in Heterogeneous Human Populations.
Cell Syst
2016
27587673
CoLoRMap: Correcting Long Reads by Mapping short reads.
Bioinformatics
2016
27666543
The lncRNA landscape of breast cancer reveals a role for DSCAM-AS1 in breast cancer progression.
Nat Commun
2016
27776113
Comparison of high-throughput sequencing data compression tools.
Nat Methods
2016
25568283
Clonality inference in multiple tumor samples using phylogeny.
Bioinformatics
2015
26382624
Robustness of Massively Parallel Sequencing Platforms.
PLoS One
2015
1 - 50 of 105
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