Results 11 to 20 of about 3,312,497 (352)

Peeling Sequences

open access: yesMathematics, 2022
Given an n-element point set in the plane, in how many ways can it be peeled off until no point remains? Only one extreme point can be removed at a time. The answer obviously depends on the point set. If the points are in convex position, there are exactly n! ways, which is the maximum number of ways for n points. But what is the minimum number?
Adrian Dumitrescu, Géza Tóth
openaire   +6 more sources

Sequencing technologies and genome sequencing [PDF]

open access: yesJournal of Applied Genetics, 2011
The high-throughput - next generation sequencing (HT-NGS) technologies are currently the hottest topic in the field of human and animals genomics researches, which can produce over 100 times more data compared to the most sophisticated capillary sequencers based on the Sanger method.
Pareek, Chandra Shekhar   +2 more
openaire   +3 more sources

Recognizing Sequences of Sequences

open access: yesPLoS Computational Biology, 2009
The brain's decoding of fast sensory streams is currently impossible to emulate, even approximately, with artificial agents. For example, robust speech recognition is relatively easy for humans but exceptionally difficult for artificial speech recognition systems.
Kiebel, S J   +3 more
openaire   +7 more sources

Tournament Sequences and Meeussen Sequences [PDF]

open access: yesThe Electronic Journal of Combinatorics, 2000
A tournament sequence is an increasing sequence of positive integers $(t_1,t_2,\ldots)$ such that $t_1=1$ and $t_{i+1} \leq 2t_i$. A Meeussen sequence is an increasing sequence of positive integers $(m_1,m_2,\ldots)$ such that $m_1=1$, every nonnegative integer is the sum of a subset of the $\{m_i\}$, and each integer $m_i-1$ is the sum of a unique ...
Cook, Matthew, Kleber, Michael
openaire   +4 more sources

Legislative and Administrative Processes. By Hans A. Linde and George Bunn; Introduction to the American Public Law System: Cases and Materials. By Jerry L. Mashaw and Richard A. Merrill [PDF]

open access: yes, 1977
Background: Genome and transcriptome sequencing applications that rely on variation in sequence depth can be negatively affected if there are systematic biases in coverage.
Ekblom, Robert   +2 more
core   +2 more sources

Genomic variant benchmark: if you cannot measure it, you cannot improve it

open access: yesGenome Biology, 2023
Genomic benchmark datasets are essential to driving the field of genomics and bioinformatics. They provide a snapshot of the performances of sequencing technologies and analytical methods and highlight future challenges.
Sina Majidian   +4 more
doaj   +1 more source

An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing. [PDF]

open access: yes, 2018
Sequencing technologies have undergone a paradigm shift from bulk to single-cell resolution in response to an evolving understanding of the role of cellular heterogeneity in biological systems.
Abate, Adam R   +3 more
core   +2 more sources

Deep convolutional neural networks for accurate somatic mutation detection

open access: yesNature Communications, 2019
Somatic mutations are crucial to the understanding of cancer genesis, progression, and treatment, but are still challenging to detect. Here the authors present NeuSomatic, a convolutional neural network approach for accurate somatic mutation detection ...
Sayed Mohammad Ebrahim Sahraeian   +5 more
doaj   +1 more source

SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads

open access: yesBMC Genomics, 2017
Background Characterization of genomic structural variation (SV) is essential to expanding the research and clinical applications of genome sequencing.
Oliver A. Hampton   +10 more
doaj   +1 more source

Plasma-based longitudinal mutation monitoring as a potential predictor of disease progression in subjects with adenocarcinoma in advanced non-small cell lung cancer

open access: yesBMC Cancer, 2020
Background Identifying and tracking somatic mutations in cell-free DNA (cfDNA) by next-generation sequencing (NGS) has the potential to transform the clinical management of subjects with advanced non-small cell lung cancer (NSCLC). Methods Baseline tumor
John Jiang   +14 more
doaj   +1 more source

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