User profiles for L. Maretty
Lasse MarettyAarhus University Verified email at clin.au.dk Cited by 1247 |
[HTML][HTML] Next-generation biology: sequencing and data analysis approaches for non-model organisms
…, J Ramos-Madrigal, JA Sibbesen, L Maretty… - Marine genomics, 2016 - Elsevier
As sequencing technologies become more affordable, it is now realistic to propose studying
the evolutionary history of virtually any organism on a genomic scale. However, when …
the evolutionary history of virtually any organism on a genomic scale. However, when …
[HTML][HTML] An integrated multi-omics analysis identifies prognostic molecular subtypes of non-muscle-invasive bladder cancer
The molecular landscape in non-muscle-invasive bladder cancer (NMIBC) is characterized
by large biological heterogeneity with variable clinical outcomes. Here, we perform an …
by large biological heterogeneity with variable clinical outcomes. Here, we perform an …
[HTML][HTML] Circular DNA elements of chromosomal origin are common in healthy human somatic tissue
The human genome is generally organized into stable chromosomes, and only tumor cells
are known to accumulate kilobase (kb)-sized extrachromosomal circular DNA elements (…
are known to accumulate kilobase (kb)-sized extrachromosomal circular DNA elements (…
Metallothionein‐I+ II in neuroprotection
Metallothionein (MT)‐I+II synthesis is induced in the central nervous system (CNS) in response
to practically any pathogen or disorder, where it is increased mainly in reactive glia. MT‐I…
to practically any pathogen or disorder, where it is increased mainly in reactive glia. MT‐I…
[HTML][HTML] Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
Hundreds of thousands of human genomes are now being sequenced to characterize genetic
variation and use this information to augment association mapping studies of complex …
variation and use this information to augment association mapping studies of complex …
[HTML][HTML] Bayesian transcriptome assembly
RNA sequencing allows for simultaneous transcript discovery and quantification, but
reconstructing complete transcripts from such data remains difficult. Here, we introduce …
reconstructing complete transcripts from such data remains difficult. Here, we introduce …
[HTML][HTML] Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads
Background Circular DNA has recently been identified across different species including
human normal and cancerous tissue, but short-read mappers are unable to align many of the …
human normal and cancerous tissue, but short-read mappers are unable to align many of the …
Accurate genotyping across variant classes and lengths using variant graphs
JA Sibbesen, L Maretty… - Nature …, 2018 - nature.com
Genotype estimates from short-read sequencing data are typically based on the alignment
of reads to a linear reference, but reads originating from more complex variants (for example, …
of reads to a linear reference, but reads originating from more complex variants (for example, …
Facile photochemical synthesis and characterization of highly fluorescent silver nanoparticles
L Maretti, PS Billone, Y Liu… - Journal of the American …, 2009 - ACS Publications
Highly fluorescent silver nanoparticles (AgFNP) have been prepared by a facile
photochemical method, yielding these materials in just a few minutes and with excellent long-term …
photochemical method, yielding these materials in just a few minutes and with excellent long-term …
Unsupervised detection of fragment length signatures of circulating tumor DNA using non-negative matrix factorization
Sequencing of cell-free DNA (cfDNA) is currently being used to detect cancer by searching
both for mutational and non-mutational alterations. Recent work has shown that the length …
both for mutational and non-mutational alterations. Recent work has shown that the length …