Demo Data from EDBT 2026 / reviewers in the wild / expert
Sjoerd van den Belt
dblp:394/4345
· DBLP profile ↗
1ranked-venue papers
1as first author
1since 2021 · last 2024
0009-0005-8812-9929ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 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
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
population genetics |
0.8 | 1 | 2024 | Scalable CNN-based classification of selective sweeps using derived allele frequencies · Bioinform. 2024 |
Bioinformatics and computational biology › population genetics › selection detection
selective sweep detection |
0.8 | 1 | 2024 | Scalable CNN-based classification of selective sweeps using derived allele frequencies · Bioinform. 2024 |
Bioinformatics and computational biology › genomics › genomic data analysis
genomic classification |
0.2 | 1 | 2024 | Scalable CNN-based classification of selective sweeps using derived allele frequencies · Bioinform. 2024 |
Methods — techniques the papers use, named apart from their topics
neural architecture search · 0.8data fusion · 0.8convolutional neural network · 0.8
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | Scalable CNN-based classification of selective sweeps using derived allele frequenciesabstractMOTIVATION: Selective sweeps can successfully be distinguished from neutral genetic data using summary statistics and likelihood-based methods that analyze single nucleotide polymorphisms (SNPs). However, these methods are sensitive to confounding factors, such as severe population bottlenecks and old migration. By virtue of machine learning, and specifically convolutional neural networks (CNNs), new accurate classification models that are robust to confounding factors have been recently proposed. However, such methods are more computationally expensive than summary-statistic-based ones, yielding them impractical for processing large-scale genomic data. Moreover, SNP data are frequently preprocessed to improve classification accuracy, further exacerbating the long analysis times. RESULTS: To this end, we propose a 1D CNN-based model, dubbed FAST-NN, that does not require any preprocessing while using only derived allele frequencies instead of summary statistics or raw SNP data, thereby yielding a sample-size-invariant, scalable solution. We evaluated several data fusion approaches to account for the variance of the density of genetic diversity across genomic regions (a selective sweep signature), and performed an extensive neural architecture search based on a state-of-the-art reference network architecture (SweepNet). The resulting model, FAST-NN, outperforms the reference architecture by up to 12% inference accuracy over all challenging evolutionary scenarios with confounding factors that were evaluated. Moreover, FAST-NN is between 30× and 259× faster on a single CPU core, and between 2.0× and 6.2× faster on a GPU, when processing sample sizes between 128 and 1000 samples. Our work paves the way for the practical use of CNNs in large-scale selective sweep detection. AVAILABILITY AND IMPLEMENTATION: https://github.com/SjoerdvandenBelt/FAST-NN. Sjoerd van den Belt, Nikolaos Alachiotis 0001 |
Bioinform. | 1 |