Chen Y, Davidson N, Kei Wan Y, Yao F, Su Y, Gamaarachchi H
Nat Methods. 2025; .
PMID: 40082608
DOI: 10.1038/s41592-025-02623-4.
Battistella E, Maheshwari A, Ekim B, Berger B, Popic V
bioRxiv. 2025; .
PMID: 40027721
PMC: 11870604.
DOI: 10.1101/2025.02.17.638151.
Beslic D, Kucklick M, Engelmann S, Fuchs S, Renard B, Korber N
Bioinformatics. 2024; 41(1).
PMID: 39710838
PMC: 11729726.
DOI: 10.1093/bioinformatics/btae744.
Dietrich V, Alagna N, Helm M, Gerber S, Butto T
Bioinformatics. 2024; 40(12).
PMID: 39657315
PMC: 11630908.
DOI: 10.1093/bioinformatics/btae665.
Zhu X, Sanz-Jimenez P, Ning X, Tahir Ul Qamar M, Chen L
Plant Commun. 2024; 5(11):101064.
PMID: 39155503
PMC: 11589328.
DOI: 10.1016/j.xplc.2024.101064.
Interactive visualization of nanopore sequencing signal data with Squigualiser.
Samarakoon H, Liyanage K, Ferguson J, Parameswaran S, Gamaarachchi H, Deveson I
Bioinformatics. 2024; 40(8).
PMID: 39137136
PMC: 11335371.
DOI: 10.1093/bioinformatics/btae501.
Machine learning empowered next generation DNA sequencing: perspective and prospectus.
Mittal S, Jena M, Pathak B
Chem Sci. 2024; 15(31):12169-12188.
PMID: 39118630
PMC: 11304540.
DOI: 10.1039/d4sc01714e.
RawHash2: mapping raw nanopore signals using hash-based seeding and adaptive quantization.
Firtina C, Soysal M, Lindegger J, Mutlu O
Bioinformatics. 2024; 40(8).
PMID: 39078113
PMC: 11333567.
DOI: 10.1093/bioinformatics/btae478.
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.
Cortese A, Beecroft S, Facchini S, Curro R, Cabrera-Serrano M, Stevanovski I
Nat Commun. 2024; 15(1):6327.
PMID: 39068203
PMC: 11283466.
DOI: 10.1038/s41467-024-49950-2.
A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus.
Pellerin D, Del Gobbo G, Couse M, Dolzhenko E, Nageshwaran S, Cheung W
Nat Genet. 2024; 56(7):1366-1370.
PMID: 38937606
PMC: 11440897.
DOI: 10.1038/s41588-024-01808-5.
Advances in long-read single-cell transcriptomics.
Kumari P, Kaur M, Dindhoria K, Ashford B, Amarasinghe S, Thind A
Hum Genet. 2024; 143(9-10):1005-1020.
PMID: 38787419
PMC: 11485027.
DOI: 10.1007/s00439-024-02678-x.
Nanopore Current Events Magnifier (nanoCEM): a novel tool for visualizing current events at modification sites of nanopore sequencing.
Guo Z, Ni Y, Tan L, Shao Y, Ye L, Chen S
NAR Genom Bioinform. 2024; 6(2):lqae052.
PMID: 38774513
PMC: 11106030.
DOI: 10.1093/nargab/lqae052.
LINE-1 retrotransposons contribute to mouse PV interneuron development.
Bodea G, Botto J, Ferreiro M, Sanchez-Luque F, de Los Rios Barreda J, Rasmussen J
Nat Neurosci. 2024; 27(7):1274-1284.
PMID: 38773348
PMC: 11239520.
DOI: 10.1038/s41593-024-01650-2.
Epitranscriptome insights into Riccia fluitans L. (Marchantiophyta) aquatic transition using nanopore direct RNA sequencing.
Mazdziarz M, Krawczyk K, Kurzynski M, Paukszto L, Szablinska-Piernik J, Szczecinska M
BMC Plant Biol. 2024; 24(1):399.
PMID: 38745128
PMC: 11094948.
DOI: 10.1186/s12870-024-05114-4.
Comparison of CcrM-dependent methylation in and by nanopore sequencing.
Campbell M, Barton I, Roop 2nd R, Chien P
J Bacteriol. 2024; 206(6):e0008324.
PMID: 38722176
PMC: 11332171.
DOI: 10.1128/jb.00083-24.
Simulation of nanopore sequencing signal data with tunable parameters.
Gamaarachchi H, Ferguson J, Samarakoon H, Liyanage K, Deveson I
Genome Res. 2024; 34(5):778-783.
PMID: 38692839
PMC: 11216307.
DOI: 10.1101/gr.278730.123.
Detection of ribonucleotides embedded in DNA by Nanopore sequencing.
Grasso L, Fonzino A, Manzari C, Leonardi T, Picardi E, Gissi C
Commun Biol. 2024; 7(1):491.
PMID: 38654143
PMC: 11039623.
DOI: 10.1038/s42003-024-06077-w.
Streamlining remote nanopore data access with slow5curl.
Wong B, Ferguson J, Do J, Gamaarachchi H, Deveson I
Gigascience. 2024; 13.
PMID: 38608279
PMC: 11010652.
DOI: 10.1093/gigascience/giae016.
A full-length 18S ribosomal DNA metabarcoding approach for determining protist community diversity using Nanopore sequencing.
Gaonkar C, Campbell L
Ecol Evol. 2024; 14(4):e11232.
PMID: 38606340
PMC: 11007259.
DOI: 10.1002/ece3.11232.
EpiDiP/NanoDiP: a versatile unsupervised machine learning edge computing platform for epigenomic tumour diagnostics.
Hench J, Hultschig C, Brugger J, Mariani L, Guzman R, Soleman J
Acta Neuropathol Commun. 2024; 12(1):51.
PMID: 38576030
PMC: 10993614.
DOI: 10.1186/s40478-024-01759-2.