Results 221 to 230 of about 327,413 (252)
Correction to: A graph clustering algorithm for detection and genotyping of structural variants from long reads. [PDF]
europepmc +1 more source
Evaluation of CircRNA Sequence Assembly Methods Using Long Reads
The functional study on circRNAs has been increasing in the past decade due to its important roles in micro RNA sponge, protein coding, the initiation, and progression of diseases.
Yin Peng, Yanjie Wei, Wei Yanjie
exaly +3 more sources
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2022
Abstract The final chapter of the book circles back to the opening question of time and reading. It returns to one kind of reading that was associated with lockdown from the beginning: of long, weighty books, often classics, whose reading is easily deferred, but whose very length supports the idea of engagement with a novel as a serious ...
Ben Davies +2 more
openaire +1 more source
Abstract The final chapter of the book circles back to the opening question of time and reading. It returns to one kind of reading that was associated with lockdown from the beginning: of long, weighty books, often classics, whose reading is easily deferred, but whose very length supports the idea of engagement with a novel as a serious ...
Ben Davies +2 more
openaire +1 more source
Metagenomics Binning of Long Reads Using Read-Overlap Graphs
Lecture Notes in Computer Science, 2022Yu Lin, Anuradha Wickramarachchi
exaly +2 more sources
Doing the Reading: The Decline of Long Long-Form Reading in Higher Education
Poetics Today, 2021Abstract Long-form reading of literary and non-literary texts is historically an essential component of education. However, in many schooling contexts, the amount of long-form reading is diminishing. Are digital technologies augmenting this trend? And are these technologies affecting assignments and student reading patterns in other ways?
Naomi S. Baron, Anne Mangen
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A long read of the human genome
Nature Reviews Genetics, 2020A study in Nature describes the assembly of a human genome with greater continuity than the current reference genome, as well as the assembly of a complete human X chromosome. These assemblies were achieved by combining data generated by different long-read sequencing technologies.
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Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads
The Illumina DNA sequencing platform generates accurate but short reads, which can be used to produce accurate but fragmented genome assemblies. Pacific Biosciences and Oxford Nanopore Technologies DNA sequencing platforms generate long reads that can ...
Ryan Wick, Claire Gorrie, Louise Judd
exaly +2 more sources
2014
We present here the results of a study focused on text reading in a car. The purpose of this work is to explore how machine synthesized reading is perceived by users. Are the users willing to tolerate deficiencies of machine synthesized speech and trade it off for more current content? What is the impact of listening to it on driver’s distraction?
Ladislav Kunc +7 more
openaire +1 more source
We present here the results of a study focused on text reading in a car. The purpose of this work is to explore how machine synthesized reading is perceived by users. Are the users willing to tolerate deficiencies of machine synthesized speech and trade it off for more current content? What is the impact of listening to it on driver’s distraction?
Ladislav Kunc +7 more
openaire +1 more source
Genomics in the long-read sequencing era
Trends in Genetics, 2023Long-read sequencing (LRS) technologies have provided extremely powerful tools to explore genomes. While in the early years these methods suffered technical limitations, they have recently made significant progress in terms of read length, throughput, and accuracy and bioinformatics tools have strongly improved.
Erwin L, van Dijk +6 more
openaire +2 more sources
Democratizing long-read genome assembly
Cell Systems, 2021De novo assembled genomes serve as the backbone for modern genomics. In an article in this issue of Cell Systems, Ekim et al. present the mdBG assembler that can assemble genomes 100-fold faster than previous methods, including a human genome in under 10 min, which unlocks pan-genomics for many species.
Melanie, Kirsche, Michael C, Schatz
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