Demo Data from EDBT 2026 / reviewers in the wild / expert
Guillaume J. Filion
dblp:164/0870
· DBLP profile ↗
3ranked-venue papers
0as first author
0since 2021 · last 2017
0000-0002-3473-1632ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 3
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 6 heaviest of 7, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › epigenomics
ChIP-seq analysis |
0.2 | 1 | 2016 | Zerone: a ChIP-seq discretizer for multiple replicates with built-in quality control · Bioinform. 2016 |
Bioinformatics and computational biology › sequence analysis
error correction |
0.2 | 1 | 2015 | Starcode: sequence clustering based on all-pairs search · Bioinform. 2015 |
Bioinformatics and computational biology
sequence analysis |
0.2 | 1 | 2015 | Starcode: sequence clustering based on all-pairs search · Bioinform. 2015 |
Bioinformatics and computational biology › sequence analysis
sequence clustering |
0.2 | 1 | 2015 | Starcode: sequence clustering based on all-pairs search · Bioinform. 2015 |
Bioinformatics and computational biology › sequence alignment
pairwise sequence alignment |
0.1 | 1 | 2015 | Starcode: sequence clustering based on all-pairs search · Bioinform. 2015 |
Bioinformatics and computational biology
sequence alignment |
0.1 | 1 | 2015 | Starcode: sequence clustering based on all-pairs search · Bioinform. 2015 |
Methods — techniques the papers use, named apart from their topics
support vector machine · 0.2hidden markov model · 0.2trie · 0.2needleman-wunsch algorithm · 0.2levenshtein distance · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2017 | Automatic analysis and 3D-modelling of Hi-C data using TADbit reveals structural features of the fly chromatin colorsabstractThe sequence of a genome is insufficient to understand all genomic processes carried out in the cell nucleus. To achieve this, the knowledge of its three-dimensional architecture is necessary. Advances in genomic technologies and the development of new analytical methods, such as Chromosome Conformation Capture (3C) and its derivatives, provide unprecedented insights in the spatial organization of genomes. Here we present TADbit, a computational framework to analyze and model the chromatin fiber in three dimensions. Our package takes as input the sequencing reads of 3C-based experiments and performs the following main tasks: (i) pre-process the reads, (ii) map the reads to a reference genome, (iii) filter and normalize the interaction data, (iv) analyze the resulting interaction matrices, (v) build 3D models of selected genomic domains, and (vi) analyze the resulting models to characterize their structural properties. To illustrate the use of TADbit, we automatically modeled 50 genomic domains from the fly genome revealing differential structural features of the previously defined chromatin colors, establishing a link between the conformation of the genome and the local chromatin composition. TADbit provides three-dimensional models built from 3C-based experiments, which are ready for visualization and for characterizing their relation to gene expression and epigenetic states. TADbit is an open-source Python library available for download from https://github.com/3DGenomes/tadbit. François Serra, Davide Baù, Mike Goodstadt, David Castillo, Guillaume J. Filion, Marc A. Martí-Renom |
PLoS Comput. Biol. | 5 |
| 2016 | Zerone: a ChIP-seq discretizer for multiple replicates with built-in quality controlabstractMOTIVATION: Chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq) is the standard method to investigate chromatin protein composition. As the number of community-available ChIP-seq profiles increases, it becomes more common to use data from different sources, which makes joint analysis challenging. Issues such as lack of reproducibility, heterogeneous quality and conflicts between replicates become evident when comparing datasets, especially when they are produced by different laboratories. RESULTS: Here, we present Zerone, a ChIP-seq discretizer with built-in quality control. Zerone is powered by a Hidden Markov Model with zero-inflated negative multinomial emissions, which allows it to merge several replicates into a single discretized profile. To identify low quality or irreproducible data, we trained a Support Vector Machine and integrated it as part of the discretization process. The result is a classifier reaching 95% accuracy in detecting low quality profiles. We also introduce a graphical representation to compare discretization quality and we show that Zerone achieves outstanding accuracy. Finally, on current hardware, Zerone discretizes a ChIP-seq experiment on mammalian genomes in about 5 min using less than 700 MB of memory. AVAILABILITY AND IMPLEMENTATION: Zerone is available as a command line tool and as an R package. The C source code and R scripts can be downloaded from https://github.com/nanakiksc/zerone The information to reproduce the benchmark and the figures is stored in a public Docker image that can be downloaded from https://hub.docker.com/r/nanakiksc/zerone/ CONTACT: : [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Pol Cuscó, Guillaume J. Filion |
Bioinform. | 2 |
| 2015 | Starcode: sequence clustering based on all-pairs searchabstractMOTIVATION: The increasing throughput of sequencing technologies offers new applications and challenges for computational biology. In many of those applications, sequencing errors need to be corrected. This is particularly important when sequencing reads from an unknown reference such as random DNA barcodes. In this case, error correction can be done by performing a pairwise comparison of all the barcodes, which is a computationally complex problem. RESULTS: Here, we address this challenge and describe an exact algorithm to determine which pairs of sequences lie within a given Levenshtein distance. For error correction or redundancy reduction purposes, matched pairs are then merged into clusters of similar sequences. The efficiency of starcode is attributable to the poucet search, a novel implementation of the Needleman-Wunsch algorithm performed on the nodes of a trie. On the task of matching random barcodes, starcode outperforms sequence clustering algorithms in both speed and precision. AVAILABILITY AND IMPLEMENTATION: The C source code is available at http://github.com/gui11aume/starcode. Eduard Zorita, Pol Cuscó, Guillaume J. Filion |
Bioinform. | 3 |