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Sergey Nurk

dblp:122/8985 · DBLP profile ↗
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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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis › sequence assembly
genome assembly
0.632016
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
0.422016
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
0.212014
ExSPAnder: a universal repeat resolver for DNA fragment assembly · Bioinform. 2014
Bioinformatics and computational biology › sequence analysis › sequence assembly › genome assembly
repeat resolution
0.212014
ExSPAnder: a universal repeat resolver for DNA fragment assembly · Bioinform. 2014
Bioinformatics and computational biology › single-cell analysis
single-cell sequencing
0.112014
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
YearPublicationVenuePosition
2020 SPAligner: alignment of long diverged molecular sequences to assembly graphs
abstract
BACKGROUND: 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
RECOMB1
2014 ExSPAnder: a universal repeat resolver for DNA fragment assembly
abstract
UNLABELLED: 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
RECOMB1