Demo Data from EDBT 2026 / reviewers in the wild / expert
Sergey Nurk
dblp:122/8985
· DBLP profile ↗
4ranked-venue papers
2as first author
0since 2021 · last 2020
0000-0003-1301-5749ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 4 · 2 first-author
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
3 papers |
Bioinformatics and computational biology · 100% |
Topics — the 5 heaviest of 5, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › sequence analysis › sequence assembly
genome assembly |
0.6 | 3 | 2016 | metaSPAdes: A New Versatile de novo Metagenomics Assembler · RECOMB 2016 ExSPAnder: a universal repeat resolver for DNA fragment assembly · Bioinform. 2014 Assembling Genomes and Mini-metagenomes from Highly Chimeric Reads · RECOMB 2013 |
Bioinformatics and computational biology › metagenomics
metagenomic assembly |
0.4 | 2 | 2016 | metaSPAdes: A New Versatile de novo Metagenomics Assembler · RECOMB 2016 Assembling Genomes and Mini-metagenomes from Highly Chimeric Reads · RECOMB 2013 |
Bioinformatics and computational biology
genomics |
0.2 | 1 | 2014 | ExSPAnder: a universal repeat resolver for DNA fragment assembly · Bioinform. 2014 |
Bioinformatics and computational biology › sequence analysis › sequence assembly › genome assembly
repeat resolution |
0.2 | 1 | 2014 | ExSPAnder: a universal repeat resolver for DNA fragment assembly · Bioinform. 2014 |
Bioinformatics and computational biology › single-cell analysis
single-cell sequencing |
0.1 | 1 | 2014 | ExSPAnder: a universal repeat resolver for DNA fragment assembly · Bioinform. 2014 |
Methods — techniques the papers use, named apart from their topics
de bruijn graph · 0.2read-pair analysis · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2020 | SPAligner: alignment of long diverged molecular sequences to assembly graphsabstractBACKGROUND: Graph-based representation of genome assemblies has been recently used in different contexts - from improved reconstruction of plasmid sequences and refined analysis of metagenomic data to read error correction and reference-free haplotype reconstruction. While many of these applications heavily utilize the alignment of long nucleotide sequences to assembly graphs, first general-purpose software tools for finding such alignments have been released only recently and their deficiencies and limitations are yet to be discovered. Moreover, existing tools can not perform alignment of amino acid sequences, which could prove useful in various contexts - in particular the analysis of metagenomic sequencing data. RESULTS: In this work we present a novel SPAligner (Saint-Petersburg Aligner) tool for aligning long diverged nucleotide and amino acid sequences to assembly graphs. We demonstrate that SPAligner is an efficient solution for mapping third generation sequencing reads onto assembly graphs of various complexity and also show how it can facilitate the identification of known genes in complex metagenomic datasets. CONCLUSIONS: Our work will facilitate accelerating the development of graph-based approaches in solving sequence to genome assembly alignment problem. SPAligner is implemented as a part of SPAdes tools library and is available on Github. Tatiana Dvorkina, Dmitry Antipov, Anton I. Korobeynikov, Sergey Nurk |
BMC Bioinform. | 4 |
| 2016 | metaSPAdes: A New Versatile de novo Metagenomics Assembler
Sergey Nurk, Dmitry Meleshko, Anton I. Korobeynikov, Pavel A. Pevzner |
RECOMB | 1 |
| 2014 | ExSPAnder: a universal repeat resolver for DNA fragment assemblyabstractUNLABELLED: Next-generation sequencing (NGS) technologies have raised a challenging de novo genome assembly problem that is further amplified in recently emerged single-cell sequencing projects. While various NGS assemblers can use information from several libraries of read-pairs, most of them were originally developed for a single library and do not fully benefit from multiple libraries. Moreover, most assemblers assume uniform read coverage, condition that does not hold for single-cell projects where utilization of read-pairs is even more challenging. We have developed an exSPAnder algorithm that accurately resolves repeats in the case of both single and multiple libraries of read-pairs in both standard and single-cell assembly projects. AVAILABILITY AND IMPLEMENTATION: http://bioinf.spbau.ru/en/spades Andrey D. Prjibelski, Irina Vasilinetc, Anton Bankevich, Alexey A. Gurevich, Tatiana Krivosheeva, Sergey Nurk, Son K. Pham, Anton I. Korobeynikov, Alla L. Lapidus, Pavel A. Pevzner |
Bioinform. | 6 |
| 2013 | Assembling Genomes and Mini-metagenomes from Highly Chimeric Reads
Sergey Nurk, Anton Bankevich, Dmitry Antipov, Alexey A. Gurevich, Anton I. Korobeynikov, Alla L. Lapidus, Andrey D. Prjibelski, Alex Pyshkin, Alexander Sirotkin 0001, Yakov Sirotkin, Ramunas Stepanauskas, Jeffrey S. McLean, Roger Lasken, Scott R. Clingenpeel, Tanja Woyke, Glenn Tesler, Max A. Alekseyev, Pavel A. Pevzner |
RECOMB | 1 |