Zobrazeno 1 - 10
of 419
pro vyhledávání: '"Split-Decomposition Method"'
Autor:
Ryan Wick, Kathryn Holt
Publikováno v:
PLoS Computational Biology, Vol 18, Iss 1, p e1009802 (2022)
PLoS Computational Biology
PLoS Computational Biology
Long-read-only bacterial genome assemblies usually contain residual errors, most commonly homopolymer-length errors. Short-read polishing tools can use short reads to fix these errors, but most rely on short-read alignment which is unreliable in repe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a391a69e05764db835e0c757a49ced4a
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 10 (2021)
PLoS ONE, Vol 16, Iss 10 (2021)
The glycoside hydrolase 19 (GH19) is a bifunctional family of chitinases and endolysins, which have been studied for the control of plant fungal pests, the recycle of chitin biomass, and the treatment of multi-drug resistant bacteria. The GH19 domain
Autor:
Clara Delahaye, Jacques Nicolas
Publikováno v:
PLoS ONE
PLoS ONE, 2021, pp.1-29. ⟨10.1371/journal.pone.0257521⟩
PLoS ONE, Public Library of Science, 2021, pp.1-29. ⟨10.1371/journal.pone.0257521⟩
PLoS ONE, Vol 16, Iss 10, p e0257521 (2021)
PLoS ONE, 2021, pp.1-29. ⟨10.1371/journal.pone.0257521⟩
PLoS ONE, Public Library of Science, 2021, pp.1-29. ⟨10.1371/journal.pone.0257521⟩
PLoS ONE, Vol 16, Iss 10, p e0257521 (2021)
International audience; Oxford Nanopore Technologies' (ONT) long read sequencers offer access to longer DNA fragments than previous sequencer generations, at the cost of a higher error rate. While many papers have studied read correction methods, few
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1325d627cafd5537be7fbe871aa61be0
https://hal.inria.fr/hal-03362956
https://hal.inria.fr/hal-03362956
Publikováno v:
PLoS Computational Biology, Vol 17, Iss 10, p e1009541 (2021)
PLoS Computational Biology, Vol 17, Iss 10 (2021)
PLoS Computational Biology
PLoS Computational Biology, Vol 17, Iss 10 (2021)
PLoS Computational Biology
We have developed the program TwinCons, to detect noisy signals of deep ancestry of proteins or nucleic acids. As input, the program uses a composite alignment containing pre-defined groups, and mathematically determines a ‘cost’ of transforming
Publikováno v:
PLoS Computational Biology
PLoS Computational Biology, Vol 17, Iss 8, p e1009278 (2021)
PLoS Computational Biology, Vol 17, Iss 8, p e1009278 (2021)
CPA/AT transporters are made up of scaffold and a core domain. The core domain contains two non-canonical helices (broken or reentrant) that mediate the transport of ions, amino acids or other charged compounds. During evolution, these transporters h
Autor:
Javier S. Utgés, Geoffrey J. Barton, Stuart A. MacGowan, Noah J. M. Dietrich, Maxim I. Tsenkov
Publikováno v:
PLoS Computational Biology, Vol 17, Iss 8, p e1009335 (2021)
PLoS Computational Biology
PLoS Computational Biology
Ankyrin protein repeats bind to a wide range of substrates and are one of the most common protein motifs in nature. Here, we collate a high-quality alignment of 7,407 ankyrin repeats and examine for the first time, the distribution of human populatio
Publikováno v:
PLoS Computational Biology, Vol 17, Iss 7, p e1009244 (2021)
PLoS Computational Biology
PLoS Computational Biology
The large amount of biological data available in the current times, makes it necessary to use tools and applications based on sophisticated and efficient algorithms, developed in the area of bioinformatics. Further, access to high performance computi
Publikováno v:
PLoS Genetics, Vol 17, Iss 3, p e1009221 (2021)
PLoS Genetics
PLoS Genetics
Funder: European Molecular Biology Laboratory; funder-id: http://dx.doi.org/10.13039/100013060
Funder: University of Cambridge
Many complex genomic rearrangements arise through template switch errors, which occur in DNA replication when the
Funder: University of Cambridge
Many complex genomic rearrangements arise through template switch errors, which occur in DNA replication when the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64cf752d3d1ef5a4419f781daae71f5f
Autor:
Daniel R. O'Brien, Mrunal Dehankar, Jean Pierre A. Kocher, Ravishankar K. Iyer, Zachary D. Stephens, Lewis R. Roberts
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0250915 (2021)
PLoS ONE
PLoS ONE
The integration of viruses into the human genome is known to be associated with tumorigenesis in many cancers, but the accurate detection of integration breakpoints from short read sequencing data is made difficult by human-viral homologies, viral ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c2654667f70bf3a65c55d3e641f5bb3
https://doi.org/10.1101/2021.04.19.440427
https://doi.org/10.1101/2021.04.19.440427
Autor:
Vladimir Smirnov
Publikováno v:
PLoS Computational Biology
PLoS Computational Biology, Vol 17, Iss 10, p e1008950 (2021)
PLoS Computational Biology, Vol 17, Iss 10, p e1008950 (2021)
Multiple sequence alignment tools struggle to keep pace with rapidly growing sequence data, as few methods can handle large datasets while maintaining alignment accuracy. We recently introduced MAGUS, a new state-of-the-art method for aligning large
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f936ecba0b302713fb63eb3397138d9
https://doi.org/10.1101/2021.04.09.439137
https://doi.org/10.1101/2021.04.09.439137