Bernhard Y. Renard

Orcid: 0000-0003-4589-9809

According to our database1, Bernhard Y. Renard authored at least 41 papers between 2008 and 2023.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

Online presence:

On csauthors.net:

Bibliography

2023
MpoxRadar: a worldwide MPXV genomic surveillance dashboard.
Nucleic Acids Res., July, 2023

Comprehensive evaluation of peptide <i>de novo</i> sequencing tools for monoclonal antibody assembly.
Briefings Bioinform., January, 2023

LazyFox: fast and parallelized overlapping community detection in large graphs.
PeerJ Comput. Sci., 2023

HiClass: a Python Library for Local Hierarchical Classification Compatible with Scikit-learn.
J. Mach. Learn. Res., 2023

Identifying Drivers of Predictive Uncertainty using Variance Feature Attribution.
CoRR, 2023

SimbaML: Connecting Mechanistic Models and Machine Learning with Augmented Data.
Proceedings of the First Tiny Papers Track at ICLR 2023, 2023

2022
Ad hoc learning of peptide fragmentation from mass spectra enables an interpretable detection of phosphorylated and cross-linked peptides.
Nat. Mach. Intell., 2022

CovRadar: continuously tracking and filtering SARS-CoV-2 mutations for genomic surveillance.
Bioinform., 2022

2021
Deep learning-based real-time detection of novel pathogens during sequencing.
Briefings Bioinform., 2021

2020
An environment for sustainable research software in Germany and beyond: current state, open challenges, and call for action.
F1000Research, 2020

An Environment for Sustainable Research Software in Germany and Beyond: Current State, Open Challenges, and Call for Action.
CoRR, 2020

ganon: precise metagenomics classification against large and up-to-date sets of reference sequences.
Bioinform., 2020

DeePaC: predicting pathogenic potential of novel DNA with reverse-complement neural networks.
Bioinform., 2020

Predicting bacterial virulence factors - evaluation of machine learning and negative data strategies.
Briefings Bioinform., 2020

2019
Where did you come from, where did you go: Refining metagenomic analysis tools for horizontal gene transfer characterisation.
PLoS Comput. Biol., 2019

Computational pan-genome mapping and pairwise SNP-distance improve detection of Mycobacterium tuberculosis transmission clusters.
PLoS Comput. Biol., 2019

2018
LiveKraken--real-time metagenomic classification of illumina data.
Bioinform., 2018

PriLive: privacy-preserving real-time filtering for next-generation sequencing.
Bioinform., 2018

DREAM-Yara: an exact read mapper for very large databases with short update time.
Bioinform., 2018

PAIPline: pathogen identification in metagenomic and clinical next generation sequencing samples.
Bioinform., 2018

Evaluating de novo sequencing in proteomics: already an accurate alternative to database-driven peptide identification?
Briefings Bioinform., 2018

2017
HiLive: real-time mapping of illumina reads while sequencing.
Bioinform., 2017

Abundance estimation and differential testing on strain level in metagenomics data.
Bioinform., 2017

2016
Detecting horizontal gene transfer by mapping sequencing reads across species boundaries.
Bioinform., 2016

DUDes: a top-down taxonomic profiler for metagenomics.
Bioinform., 2016

iPQF: a new peptide-to-protein summarization method using peptide spectra characteristics to improve protein quantification.
Bioinform., 2016

2015
SuRankCo: supervised ranking of contigs in de novo assemblies.
BMC Bioinform., 2015

MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms.
Bioinform., 2015

Docking small peptides remains a great challenge: an assessment using AutoDock Vina.
Briefings Bioinform., 2015

2014
GIIRA - RNA-Seq driven gene finding incorporating ambiguous reads.
Bioinform., 2014

Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics.
Bioinform., 2014

Specificity control for read alignments using an artificial reference genome-guided false discovery rate.
Bioinform., 2014

RNA-seq driven gene identification.
Proceedings of the German conference on bioinformatics 2014, September 28, 2014

2013
Analyzing genome coverage profiles with applications to quality control in metagenomics.
Bioinform., 2013

2012
Confidence-based Somatic Mutation Evaluation and Prioritization.
PLoS Comput. Biol., 2012

2011
rapmad: Robust Analysis of Peptide Microarray Data.
BMC Bioinform., 2011

SIMA: Simultaneous Multiple Alignment of LC/MS Peak Lists.
Bioinform., 2011

2010
Deuteration distribution estimation with improved sequence coverage for HX/MS experiments.
Bioinform., 2010

Computational protein profile similarity screening for quantitative mass spectrometry experiments.
Bioinform., 2010

2009
Multivariate Watershed Segmentation of Compositional Data.
Proceedings of the Discrete Geometry for Computer Imagery, 2009

2008
NITPICK: peak identification for mass spectrometry data.
BMC Bioinform., 2008


  Loading...