Results 51 to 60 of about 12,005,683 (347)

Long-read sequencing settings for efficient structural variation detection based on comprehensive evaluation

open access: yesBMC Bioinformatics, 2021
Background With the rapid development of long-read sequencing technologies, it is possible to reveal the full spectrum of genetic structural variation (SV).
Tao Jiang   +6 more
doaj   +1 more source

Benchmarking of Nanopore R10.4 and R9.4.1 flow cells in single-cell whole-genome amplification and whole-genome shotgun sequencing

open access: yesComputational and Structural Biotechnology Journal, 2023
Third-generation sequencing can be used in human cancer genomics and epigenomic research. Oxford Nanopore Technologies (ONT) recently released R10.4 flow cell, which claimed an improved read accuracy compared to R9.4.1 flow cell. To evaluate the benefits
Ying Ni   +4 more
doaj   +1 more source

Timing of Antisynchronous Calling: A Case Study in a Harbor Seal Pup (Phoca vitulina)

open access: yesJournal of Comparative Psychology, 2019
Alternative mathematical models predict differences in how animals adjust the timing of their calls. Differences can be measured as the effect of the timing of a conspecific call on the rate and period of calling of a focal animal, and the lag between ...
A. Ravignani
semanticscholar   +1 more source

Psychosocial Outcomes in Patients With Endocrine Tumor Syndromes: A Systematic Review

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction The combination of disease manifestations, the familial burden, and varying penetrance of endocrine tumor syndromes (ETSs) is unique. This review aimed to portray and summarize available data on psychosocial outcomes in patients with ETSs and explore gaps and opportunities for future research and care.
Daniël Zwerus   +6 more
wiley   +1 more source

A Bayesian framework to identify methylcytosines from high-throughput bisulfite sequencing data.

open access: yesPLoS Computational Biology, 2014
High-throughput bisulfite sequencing technologies have provided a comprehensive and well-fitted way to investigate DNA methylation at single-base resolution. However, there are substantial bioinformatic challenges to distinguish precisely methylcytosines
Qing Xie   +9 more
doaj   +1 more source

Factors affecting availability for detection: An example using radio-collared Northern Bobwhite (Colinus virginianus). [PDF]

open access: yesPLoS ONE, 2017
Avian monitoring strategies are usually linked to bird singing or calling behavior. Individual availability for detection can change as a result of conspecific factors affecting bird behavior, though the magnitude of these effects is difficult to ...
Christopher M Lituma   +5 more
doaj   +1 more source

A User Guide to Current Statistics on the Employment of People with Disabilities-Research Brief [PDF]

open access: yes, 2003
A MAJOR DEBATE is taking place over reports of an unprecedented decline in the employment rate of working age people with disabilities over the 1990s business cycle (1989-2000) by those using currently available national representative data sources.
Burkhauser, Richard V   +2 more
core   +3 more sources

Anthropogenic substrate-borne vibrations impact anuran calling

open access: yesScientific Reports, 2019
Anthropogenic disturbance is a major cause of the biodiversity crisis. Nevertheless, the role of anthropogenic substrate vibrations in disrupting animal behavior is poorly understood.
V. Caorsi   +9 more
semanticscholar   +1 more source

Nutritional and Behavioral Intervention for Long‐Term Childhood Acute Leukemia Survivors With Metabolic Syndrome

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Purpose Metabolic syndrome (MetS) is a common complication in survivors of childhood acute lymphoblastic and myeloid leukemia (AL), and a major risk factor for premature cardiovascular disease, type‐2‐diabetes, and metabolic dysfunction‐associated steatotic liver disease (MASLD).
Visentin Sandrine   +10 more
wiley   +1 more source

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

open access: yesGenome Medicine, 2017
Bioinformatic analysis of genomic sequencing data to identify somatic mutations in cancer samples is far from achieving the required robustness and standardisation.
M. Callari   +6 more
semanticscholar   +1 more source

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