Results 131 to 140 of about 5,268,956 (336)

Genomic and Genetic Database Resources for the Grasses [PDF]

open access: yesPlant Physiology, 2009
In the strict sense, a biological database is not a Web site. However, the interface that a researcher uses to access the data stored within a database is almost always a Web site. Nonetheless, the two terms are synonymous in the minds of most biologists.
openaire   +3 more sources

Evolving structure-function mappings in cognitive neuroscience using genetic programming [PDF]

open access: yes, 2005
A challenging goal of psychology and neuroscience is to map cognitive functions onto neuroanatomical structures. This paper shows how computational methods based upon evolutionary algorithms can facilitate the search for satisfactory mappings by ...
Gobet, F, Parker, A
core   +1 more source

Circulating tumor DNA monitoring and blood tumor mutational burden in patients with metastatic solid tumors treated with atezolizumab

open access: yesMolecular Oncology, EarlyView.
In patients treated with atezolizumab as a part of the MyPathway (NCT02091141) trial, pre‐treatment ctDNA tumor fraction at high levels was associated with poor outcomes (radiographic response, progression‐free survival, and overall survival) but better sensitivity for blood tumor mutational burden (bTMB).
Charles Swanton   +17 more
wiley   +1 more source

Genotator: A disease-agnostic tool for genetic annotation of disease

open access: yesBMC Medical Genomics, 2010
Background Disease-specific genetic information has been increasing at rapid rates as a consequence of recent improvements and massive cost reductions in sequencing technologies.
Jung Jae-Yoon   +6 more
doaj   +1 more source

SIG-DB: leveraging homomorphic encryption to Securely Interrogate privately held Genomic DataBases

open access: yes, 2018
Genomic data are becoming increasingly valuable as we develop methods to utilize the information at scale and gain a greater understanding of how genetic information relates to biological function.
Flower, Audrey   +8 more
core   +2 more sources

Evolutionary biology for the 21st century [PDF]

open access: yes, 2013
New theoretical and conceptual frameworks are required for evolutionary biology to capitalize on the wealth of data now becoming available from the study of genomes, phenotypes, and organisms - including humans - in their natural environments.Molecular ...
Arnold, Stevan J.   +14 more
core   +5 more sources

Genomics‐led approach to drug testing in models of undifferentiated pleomorphic sarcoma

open access: yesMolecular Oncology, EarlyView.
GA text Genomic data from undifferentiated pleomorphic sarcoma patients and preclinical models were used to inform a targeted drug screen. Selected compounds were tested in 2D and 3D cultures of UPS cell lines. A combination of trametinib and infigratinib was synergistic in the majority of UPS cell lines tested, which was further confirmed in an ex ...
Piotr J. Manasterski   +19 more
wiley   +1 more source

The Genetic Landscape of Diamond-Blackfan Anemia

open access: yesbioRxiv, 2018
Diamond-Blackfan anemia (DBA) is a rare bone marrow failure disorder that affects 1 in 100,000 to 200,000 live births and has been associated with mutations in components of the ribosome. In order to characterize the genetic landscape of this genetically
J. Ulirsch   +41 more
semanticscholar   +1 more source

Unraveling LINE‐1 retrotransposition in head and neck squamous cell carcinoma

open access: yesMolecular Oncology, EarlyView.
The novel RetroTest method allows the detection of L1 activation in clinical samples with low DNA input, providing global L1 activity and the identification of the L1 source element. We applied RetroTest to a real‐world cohort of HNSCC patients where we reported an early L1 activation, with more than 60% of T1 patients showing L1 activity.
Jenifer Brea‐Iglesias   +12 more
wiley   +1 more source

Classical homocystinuria: A common inborn error of metabolism? An epidemiological study based on genetic databases

open access: yesMolecular Genetics & Genomic Medicine, 2020
Background Biallelic pathogenic variants in CBS gene cause the most common form of homocystinuria, the classical homocystinuria (HCU). The worldwide prevalence of HCU is estimated to be 0.82:100,000 [95% CI, 0.39–1.73:100,000] according to clinical ...
Giovana R. Weber Hoss   +3 more
doaj   +1 more source

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