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Author Details

Serghei Mangul
School of Pharmacy, University of Southern California
2011
59
19
PMIDPaper TitleJournal TitlePublished Year
36999049RNA-seq data science: From raw data to effective interpretation.Front Genet2023
37761360The Genomic Landscape of Colorectal Cancer in the Saudi Arabian Population Using a Comprehensive Genomic Panel.Diagnostics (Basel)2023
37824736Response to 'comment on rigorous benchmarking of T cell receptor repertoire profiling methods for cancer RNA sequencing' by Davydov A.N.; Bolotin D.A.; Poslavsky S. V. and Chudakov D.M.Brief Bioinform2023
37693502Whole Blood Transcriptomics Identifies Subclasses of Pediatric Septic Shock.Res Sq2023
37609176Analytical code sharing practices in biomedical research.bioRxiv2023
37198712Meta-analysis of (single-cell method) benchmarks reveals the need for extensibility and interoperability.Genome Biol2023
36999049RNA-seq data science: From raw data to effective interpretation.Front Genet2023
37291798Rigorous benchmarking of T-cell receptor repertoire profiling methods for cancer RNA sequencing.Brief Bioinform2023
37693502Whole Blood Transcriptomics Identifies Subclasses of Pediatric Septic Shock.Res Sq2023
37609176Analytical code sharing practices in biomedical research.bioRxiv2023
37824736Response to 'comment on rigorous benchmarking of T cell receptor repertoire profiling methods for cancer RNA sequencing' by Davydov A.N.; Bolotin D.A.; Poslavsky S. V. and Chudakov D.M.Brief Bioinform2023
37761360The Genomic Landscape of Colorectal Cancer in the Saudi Arabian Population Using a Comprehensive Genomic Panel.Diagnostics (Basel)2023
37291798Rigorous benchmarking of T-cell receptor repertoire profiling methods for cancer RNA sequencing.Brief Bioinform2023
37198712Meta-analysis of (single-cell method) benchmarks reveals the need for extensibility and interoperability.Genome Biol2023
34966181Virtual meetings promise to eliminate geographical and administrative barriers and increase accessibility, diversity and inclusivity.Nat Biotechnol2022
35396471Unlocking capacities of genomics for the COVID-19 response and future pandemics.Nat Methods2022
36085557The Pioneer Advantage: Filling the blank spots on the map of genome diversity in Europe.Gigascience2022
35753701A comprehensive benchmarking of WGS-based deletion structural variant callers.Brief Bioinform2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
36548425Remote opportunities for scholars in Ukraine.Science2022
36852763TAMPA: interpretable analysis and visualization of metagenomics-based taxon abundance profiles.Gigascience2022
37496156Scientists without borders: lessons from Ukraine.Gigascience2022
34966181Virtual meetings promise to eliminate geographical and administrative barriers and increase accessibility, diversity and inclusivity.Nat Biotechnol2022
35076276Correction for Rando et al., "Pathogenesis, Symptomatology, and Transmission of SARS-CoV-2 through Analysis of Viral Genomics and Structure".mSystems2022
37496156Scientists without borders: lessons from Ukraine.Gigascience2022
35396471Unlocking capacities of genomics for the COVID-19 response and future pandemics.Nat Methods2022
35753701A comprehensive benchmarking of WGS-based deletion structural variant callers.Brief Bioinform2022
36548425Remote opportunities for scholars in Ukraine.Science2022
36852763TAMPA: interpretable analysis and visualization of metagenomics-based taxon abundance profiles.Gigascience2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
36085557The Pioneer Advantage: Filling the blank spots on the map of genome diversity in Europe.Gigascience2022
35076276Correction for Rando et al., "Pathogenesis, Symptomatology, and Transmission of SARS-CoV-2 through Analysis of Viral Genomics and Structure".mSystems2022
33948451Unlocking capacities of viral genomics for the COVID-19 pandemic response.ArXiv2021
33858487Improving the completeness of public metadata accompanying omics studies.Genome Biol2021
34002093Diversity in immunogenomics: the value and the challenge.Nat Methods2021
33948451Unlocking capacities of viral genomics for the COVID-19 pandemic response.ArXiv2021
34214168Accurate assembly of minority viral haplotypes from next-generation sequencing through efficient noise reduction.Nucleic Acids Res2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
34036652Detection of viral gene expression in risk-stratified biopsies reveals no active HPV in cutaneous squamous cell carcinoma.Exp Dermatol2021
34346485Systematic evaluation of transcriptomics-based deconvolution methods and references using thousands of clinical samples.Brief Bioinform2021
34446078Technology dictates algorithms: recent developments in read alignment.Genome Biol2021
34644550Ancestral diversity is limited in published T cell receptor sequencing studies.Immunity2021
33858487Improving the completeness of public metadata accompanying omics studies.Genome Biol2021
34644550Ancestral diversity is limited in published T cell receptor sequencing studies.Immunity2021
34446078Technology dictates algorithms: recent developments in read alignment.Genome Biol2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
34346485Systematic evaluation of transcriptomics-based deconvolution methods and references using thousands of clinical samples.Brief Bioinform2021
34214168Accurate assembly of minority viral haplotypes from next-generation sequencing through efficient noise reduction.Nucleic Acids Res2021
34036652Detection of viral gene expression in risk-stratified biopsies reveals no active HPV in cutaneous squamous cell carcinoma.Exp Dermatol2021
34002093Diversity in immunogenomics: the value and the challenge.Nat Methods2021
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Collaborators

Co-authored papers 21
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University of California Los Angeles
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Columbia University
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Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
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King Saud bin Abdulaziz Medical City for Science and Technology
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Vrije Universiteit
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Lady Davis Institute for Medical Research, Jewish General Hospital
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David Geffen School of Medicine at University of California los angeles
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National Centre for Genomic Technologies
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