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Melania Nowicka

dblp:248/8428 · DBLP profile ↗
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2ranked-venue papers
0as first author
2since 2021 · last 2022
0000-0002-2403-1042ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 100%

Topics — the 7 heaviest of 7, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
genomics
0.612022
CovRadar: continuously tracking and filtering SARS-CoV-2 mutations for genomic surveillance · Bioinform. 2022
Bioinformatics and computational biology › genomics › viral genomics
genomic surveillance
0.612022
CovRadar: continuously tracking and filtering SARS-CoV-2 mutations for genomic surveillance · Bioinform. 2022
Bioinformatics and computational biology
multiple sequence alignment
0.612022
CovRadar: continuously tracking and filtering SARS-CoV-2 mutations for genomic surveillance · Bioinform. 2022
Bioinformatics and computational biology › metagenomics
pathogen detection
0.612022
Detecting DNA of novel fungal pathogens using ResNets and a curated fungi-hosts data collection · Bioinform. 2022
Bioinformatics and computational biology
sequence analysis
0.612022
CovRadar: continuously tracking and filtering SARS-CoV-2 mutations for genomic surveillance · Bioinform. 2022
Bioinformatics and computational biology › genomics
variant calling
0.612022
CovRadar: continuously tracking and filtering SARS-CoV-2 mutations for genomic surveillance · Bioinform. 2022
Bioinformatics and computational biology › genomics › machine learning for genomics
genome representation learning
0.212022
Detecting DNA of novel fungal pathogens using ResNets and a curated fungi-hosts data collection · Bioinform. 2022

Methods — techniques the papers use, named apart from their topics

variant inference · 0.6sequence homology · 0.6resnet · 0.6multiple sequence alignment · 0.6local alignment · 0.6deep learning · 0.6
YearPublicationVenuePosition
2022 Detecting DNA of novel fungal pathogens using ResNets and a curated fungi-hosts data collection
abstract
BACKGROUND: Emerging pathogens are a growing threat, but large data collections and approaches for predicting the risk associated with novel agents are limited to bacteria and viruses. Pathogenic fungi, which also pose a constant threat to public health, remain understudied. Relevant data remain comparatively scarce and scattered among many different sources, hindering the development of sequencing-based detection workflows for novel fungal pathogens. No prediction method working for agents across all three groups is available, even though the cause of an infection is often difficult to identify from symptoms alone. RESULTS: We present a curated collection of fungal host range data, comprising records on human, animal and plant pathogens, as well as other plant-associated fungi, linked to publicly available genomes. We show that it can be used to predict the pathogenic potential of novel fungal species directly from DNA sequences with either sequence homology or deep learning. We develop learned, numerical representations of the collected genomes and visualize the landscape of fungal pathogenicity. Finally, we train multi-class models predicting if next-generation sequencing reads originate from novel fungal, bacterial or viral threats. CONCLUSIONS: The neural networks trained using our data collection enable accurate detection of novel fungal pathogens. A curated set of over 1400 genomes with host and pathogenicity metadata supports training of machine-learning models and sequence comparison, not limited to the pathogen detection task. AVAILABILITY AND IMPLEMENTATION: The data, models and code are hosted at https://zenodo.org/record/5846345, https://zenodo.org/record/5711877 and https://gitlab.com/dacs-hpi/deepac. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Jakub M. Bartoszewicz, Ferdous Nasri, Melania Nowicka, Bernhard Y. Renard
Bioinform.3
2022 CovRadar: continuously tracking and filtering SARS-CoV-2 mutations for genomic surveillance
abstract
SUMMARY: The ongoing pandemic caused by SARS-CoV-2 emphasizes the importance of genomic surveillance to understand the evolution of the virus, to monitor the viral population, and plan epidemiological responses. Detailed analysis, easy visualization and intuitive filtering of the latest viral sequences are powerful for this purpose. We present CovRadar, a tool for genomic surveillance of the SARS-CoV-2 Spike protein. CovRadar consists of an analytical pipeline and a web application that enable the analysis and visualization of hundreds of thousand sequences. First, CovRadar extracts the regions of interest using local alignment, then builds a multiple sequence alignment, infers variants and consensus and finally presents the results in an interactive app, making accessing and reporting simple, flexible and fast. AVAILABILITY AND IMPLEMENTATION: CovRadar is freely accessible at https://covradar.net, its open-source code is available at https://gitlab.com/dacs-hpi/covradar. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Alice Wittig, Fábio Miranda 0002, Martin Hölzer, Tom Altenburg, Jakub M. Bartoszewicz, Sebastian Beyvers, Marius A. Dieckmann, Ulrich Genske, Sven H. Giese, Melania Nowicka, Hugues Richard, Henning Schiebenhoefer, Anna-Juliane Schmachtenberg, Paul Sieben, Ming Tang 0008, Julius Tembrockhaus, Bernhard Y. Renard, Stephan Fuchs
Bioinform.10