Catálogo de publicaciones - libros
Elementary Functions: Algorithms and Implementation
Jean-Michel Muller
Second Edition.
Resumen/Descripción – provisto por la editorial
No disponible.
Palabras clave – provistas por la editorial
Theory of Computation; Computer System Implementation; Applications of Mathematics; Numeric Computing; Computational Science and Engineering; Mathematics of Computing
Disponibilidad
Institución detectada | Año de publicación | Navegá | Descargá | Solicitá |
---|---|---|---|---|
No detectada | 2006 | SpringerLink |
Información
Tipo de recurso:
libros
ISBN impreso
978-0-8176-4372-0
ISBN electrónico
978-0-8176-4408-6
Editor responsable
Springer Nature
País de edición
Reino Unido
Fecha de publicación
2006
Información sobre derechos de publicación
© Birkhäuser Boston 2006
Cobertura temática
Tabla de contenidos
Introduction
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
- Introduction | Pp. 1-7
Some Basic Things About Computer Arithmetic
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
- Some Basic Things About Computer Arithmetic | Pp. 9-24
Polynomial or Rational Approximations
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
Part I - Algorithms Based on Polynomial Approximation and/or Table Lookup, Multiple-Precision Evaluation of Functions | Pp. 27-66
Table-Based Methods
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
Part I - Algorithms Based on Polynomial Approximation and/or Table Lookup, Multiple-Precision Evaluation of Functions | Pp. 67-87
Multiple-Precision Evaluation of Functions
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
Part I - Algorithms Based on Polynomial Approximation and/or Table Lookup, Multiple-Precision Evaluation of Functions | Pp. 89-100
Introduction to Shift-and-Add Algorithms
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
Part II - Shift-and-Add Algorithms | Pp. 103-131
The CORDIC Algorithm
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
Part II - Shift-and-Add Algorithms | Pp. 133-156
Some Other Shift-and-Add Algorithms
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
Part II - Shift-and-Add Algorithms | Pp. 157-169
Range Reduction
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
Part III - Range Reduction, Final Rounding and Exceptions | Pp. 173-191
Final Rounding
Jean-Michel Muller
Electron tomography is an imaging technique that provides 3D images of a specimen with nanometer scale resolution. The range of specimens that can be investigated with this technique is particularly wide, from large (500–1000 nm) unique variable structures such as whole cells to suspensions of thousands of small identical macromolecules (>200 kDa).When applied to cryofixed frozen-hydrated biological material, the technique is often referred to as cryotomography. In combination with automated low-dose data collection and advanced computational methods, such as molecular identification based on pattern recognition, cryotomography can be used to visualize the architecture of small cells and organelles and/or to map macromolecular structures in their cellular environment. The resolution that can be obtained with cryotomography depends on several fundamental and technical issues related to specimen preparation, microscopy and subsequent image processing steps, but will typically be in the range of 5–10 nm.
Part III - Range Reduction, Final Rounding and Exceptions | Pp. 193-216