25 research outputs found

    A decade with vamdc: Results and ambitions

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    This paper presents an overview of the current status of the Virtual Atomic and Molecular Data Centre (VAMDC) e-infrastructure, including the current status of the VAMDC-connected (or to be connected) databases, updates on the latest technological development within the infrastructure and a presentation of some application tools that make use of the VAMDC e-infrastructure. We analyse the past 10 years of VAMDC development and operation, and assess their impact both on the field of atomic and molecular (A&amp;M) physics itself and on heterogeneous data management in international cooperation. The highly sophisticated VAMDC infrastructure and the related databases developed over this long term make them a perfect resource of sustainable data for future applications in many fields of research. However, we also discuss the current limitations that prevent VAMDC from becoming the main publishing platform and the main source of A&amp;M data for user communities, and present possible solutions under investigation by the consortium. Several user application examples are presented, illustrating the benefits of VAMDC in current research applications, which often need the A&amp;M data from more than one database. Finally, we present our vision for the future of VAMDC.</jats:p

    A Decade with VAMDC: Results and Ambitions

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    This paper presents an overview of the current status of the Virtual Atomic and Molecular Data Centre (VAMDC) e-infrastructure, including the current status of the VAMDC-connected (or to be connected) databases, updates on the latest technological development within the infrastructure and a presentation of some application tools that make use of the VAMDC e-infrastructure. We analyse the past 10 years of VAMDC development and operation, and assess their impact both on the field of atomic and molecular (A&M) physics itself and on heterogeneous data management in international cooperation. The highly sophisticated VAMDC infrastructure and the related databases developed over this long term make them a perfect resource of sustainable data for future applications in many fields of research. However, we also discuss the current limitations that prevent VAMDC from becoming the main publishing platform and the main source of A&M data for user communities, and present possible solutions under investigation by the consortium. Several user application examples are presented, illustrating the benefits of VAMDC in current research applications, which often need the A&M data from more than one database. Finally, we present our vision for the future of VAMDC

    Micropropagation and conservation of selected endangered anticancer medicinal plants from the Western Ghats of India

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    Globally, cancer is a constant battle which severely affects the human population. The major limitations of the anticancer drugs are the deleterious side effects on the quality of life. Plants play a vital role in curing many diseases with minimal or no side effects. Phytocompounds derived from various medicinal plants serve as the best source of drugs to treat cancer. The global demand for phytomedicines is mostly reached by the medicinal herbs from the tropical nations of the world even though many plant species are threatened with extinction. India is one of the mega diverse countries of the world due to its ecological habitats, latitudinal variation, and diverse climatic range. Western Ghats of India is one of the most important depositories of endemic herbs. It is found along the stretch of south western part of India and constitutes rain forest with more than 4000 diverse medicinal plant species. In recent times, many of these therapeutically valued herbs have become endangered and are being included under the red-listed plant category in this region. Due to a sharp rise in the demand for plant-based products, this rich collection is diminishing at an alarming rate that eventually triggered dangerous to biodiversity. Thus, conservation of the endangered medicinal plants has become a matter of importance. The conservation by using only in situ approaches may not be sufficient enough to safeguard such a huge bio-resource of endangered medicinal plants. Hence, the use of biotechnological methods would be vital to complement the ex vitro protection programs and help to reestablish endangered plant species. In this backdrop, the key tools of biotechnology that could assist plant conservation were developed in terms of in vitro regeneration, seed banking, DNA storage, pollen storage, germplasm storage, gene bank (field gene banking), tissue bank, and cryopreservation. In this chapter, an attempt has been made to critically review major endangered medicinal plants that possess anticancer compounds and their conservation aspects by integrating various biotechnological tool

    Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (vol 8, 1300, 2018)

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    2,6-Diphenylthiapyran-4-one

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    In the title compound, 2,6-diphenylthiacyclohexan-4-one, C17H16OSC_{17}H_{16}OS, mirror site symmetry is retained by the molecule in the solid state in the absence of CH...XC-H{...}X hydrogen bonds. The crystal structure is stabilized by van der Waals interactions, the shortest S...OS{...}O and C...OC{...} O contacts being 3.567 (2) and 3.512 (3) A, respectively

    4,8,9,10-Tetraphenyl-1,3-diazaadamantan-6-one acetone hemisolvate

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    In the title compound, C32H28N2OA~ƒA^ƒA~A^A~ƒA^A~A^0.5C3H6OC_{32}H_{28}N_{2}O·0.5C_3H_6O, the two axial and two equatorial phenyl substituents are essentially planar. There are no hydrogen-bonded interactions between the two independent molecules in the asymmetric unit. The crystal packing is characterized by CH...OC-H{...}O interactions. The solvent (acetone) molecule in the crystal structure significantly influences the packing, features of which are distinctly different from those of unsolvated 4,8,9,10-tetraphenyl-1,3-diazaadamantan-6-one and its methoxy- and chloro-substituted analogues

    4,8,9,10-Tetraphenyl-1,3-diazaadamantan-6-one

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    In the molecule of the title compound, C32H28N2OC_{32}H_{28}N_{2}O, two of the four phenyl substituents occupy axial and the other two occupy equatorial positions relative to their respective C5NC_{5}N rings of the adamantane framework. The crystal packing is characterized by weak CH...OC-H{...}O interactions. The packing features are distinctly different from those of the crystals of the methoxy- and chloro-substituted analogues
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