Serghei Mangul

Orcid: 0000-0003-4770-3443

According to our database1, Serghei Mangul authored at least 35 papers between 2011 and 2024.

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Bibliography

2024
Perceptual and technical barriers in sharing and formatting metadata accompanying omics studies.
CoRR, 2024

2023
Response 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.
Briefings Bioinform., September, 2023

Rigorous benchmarking of T-cell receptor repertoire profiling methods for cancer RNA sequencing.
Briefings Bioinform., July, 2023

MetaFast: Enabling Fast Metagenomic Classification via Seed Counting and Edit Distance Approximation.
CoRR, 2023

SequenceLab: A Comprehensive Benchmark of Computational Methods for Comparing Genomic Sequences.
CoRR, 2023

2022
Packaging, containerization, and virtualization of computational omics methods: Advances, challenges, and opportunities.
CoRR, 2022

A comprehensive benchmarking of WGS-based deletion structural variant callers.
Briefings Bioinform., 2022

TAMPA: interpretable analysis and visualization of metagenomics-based taxon abundance profiles.
Proceedings of the IEEE International Parallel and Distributed Processing Symposium, 2022

Reproducibility of Bioinformatics Tools.
Proceedings of the IEEE International Parallel and Distributed Processing Symposium, 2022

2021
Systematic evaluation of transcriptomics-based deconvolution methods and references using thousands of clinical samples.
Briefings Bioinform., 2021

A Novel Network Representation of SARS-CoV-2 Sequencing Data.
Proceedings of the Bioinformatics Research and Applications - 17th International Symposium, 2021

2020

2019
Telescope: an interactive tool for managing large scale analysis from mobile devices.
CoRR, 2019

2018
ROP: Dumpster Diving in RNA-sequencing to Find the Source of 1 Trillion Reads Across Diverse Adult Human Tissues.
Proceedings of the 2018 ACM International Conference on Bioinformatics, 2018

2017
The impact of rare variation on gene expression across tissues.
Nat., 2017

Long Single-Molecule Reads Can Resolve the Complexity of the Influenza Virus Composed of Rare, Closely Related Mutant Variants.
J. Comput. Biol., 2017

2016
HapIso: An Accurate Method for the Haplotype-Specific Isoforms Reconstruction from Long Single-Molecule Reads.
Proceedings of the Bioinformatics Research and Applications - 12th International Symposium, 2016

Reference-free comparison of microbial communities via de Bruijn graphs.
Proceedings of the 7th ACM International Conference on Bioinformatics, 2016

2015
2SNV: Quasispecies reconstruction from PacBio reads.
Proceedings of the 5th IEEE International Conference on Computational Advances in Bio and Medical Sciences, 2015

2014
Accurate viral population assembly from ultra-deep sequencing data.
Bioinform., 2014

VGA: A method for viral quasispecies assembly from ultra-deep sequencing data.
Proceedings of the IEEE 4th International Conference on Computational Advances in Bio and Medical Sciences, 2014

Deterministic regression algorithm for transcriptome frequency estimation.
Proceedings of the IEEE 4th International Conference on Computational Advances in Bio and Medical Sciences, 2014

Reconstruction of influenza a virus variants from PacBio reads.
Proceedings of the IEEE 4th International Conference on Computational Advances in Bio and Medical Sciences, 2014

2013
Transcriptome assembly and quantification from Ion Torrent RNA-Seq data.
Proceedings of the IEEE 3rd International Conference on Computational Advances in Bio and Medical Sciences, 2013

Monte-Carlo Regression algorithm for isoform frequency estimation from RNA-Seq data.
Proceedings of the IEEE 3rd International Conference on Computational Advances in Bio and Medical Sciences, 2013

2012
Improved transcriptome quantification and reconstruction from RNA-Seq reads using partial annotations.
Silico Biol., 2012

TRIP: a method for novel transcript reconstruction from paired-end RNA-seq reads.
BMC Bioinform., 2012

Workshop: Novel transcript reconstruction from paired-end RNA-Seq reads using fragment length distribution.
Proceedings of the IEEE 2nd International Conference on Computational Advances in Bio and Medical Sciences, 2012

An integer programming approach to novel transcript reconstruction from paired-end RNA-Seq reads.
Proceedings of the ACM International Conference on Bioinformatics, 2012

2011
Inferring viral quasispecies spectra from 454 pyrosequencing reads.
BMC Bioinform., 2011

Estimation of alternative splicing isoform frequencies from RNA-Seq data.
Algorithms Mol. Biol., 2011

Maximum Likelihood Estimation of Incomplete Genomic Spectrum from HTS Data.
Proceedings of the Algorithms in Bioinformatics - 11th International Workshop, 2011

Poster: Haplotype discovery from high-throughput sequencing data.
Proceedings of the IEEE 1st International Conference on Computational Advances in Bio and Medical Sciences, 2011

Poster: ViSpA: Viral spectrum assembling method.
Proceedings of the IEEE 1st International Conference on Computational Advances in Bio and Medical Sciences, 2011

RNA-Seq based discovery and reconstruction of unannotated transcripts in partially annotated genomes.
Proceedings of the 2011 IEEE International Conference on Bioinformatics and Biomedicine Workshops, 2011


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