custom written fft-based methods Search Results


90
Christof Senn fft-based analyzer
Fft Based Analyzer, supplied by Christof Senn, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Takeda fft based procedure
Fft Based Procedure, supplied by Takeda, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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RStudio fast fourier transform (fft)-based analyses
Fast Fourier Transform (Fft) Based Analyses, supplied by RStudio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Meso Scale Diagnostics LLC fast fourier transform (fft)-based homogenisation methods
Schematic illustration of the multiscale computational <t>homogenisation</t> approach considered in this paper.
Fast Fourier Transform (Fft) Based Homogenisation Methods, supplied by Meso Scale Diagnostics LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Acpharis Inc fft based sampling program piper
Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform <t>(FFT)</t> based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs <t>PIPER</t> energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003
Fft Based Sampling Program Piper, supplied by Acpharis Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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National Institute of Standards and Technology fft-based method
Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform <t>(FFT)</t> based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs <t>PIPER</t> energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003
Fft Based Method, supplied by National Institute of Standards and Technology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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National Institute of Standards and Technology nist's fft-based method
Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform <t>(FFT)</t> based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs <t>PIPER</t> energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003
Nist's Fft Based Method, supplied by National Institute of Standards and Technology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Resync LLC fft interpolation
Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform <t>(FFT)</t> based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs <t>PIPER</t> energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003
Fft Interpolation, supplied by Resync LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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NorChip AS fft processor
Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform <t>(FFT)</t> based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs <t>PIPER</t> energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003
Fft Processor, supplied by NorChip AS, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Syncrude Canada base mine lake fft
Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform <t>(FFT)</t> based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs <t>PIPER</t> energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003
Base Mine Lake Fft, supplied by Syncrude Canada, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Altera Corp fft ip core
Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform <t>(FFT)</t> based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs <t>PIPER</t> energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003
Fft Ip Core, supplied by Altera Corp, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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RStudio fft signal processing
Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform <t>(FFT)</t> based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs <t>PIPER</t> energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003
Fft Signal Processing, supplied by RStudio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Schematic illustration of the multiscale computational homogenisation approach considered in this paper.

Journal: Materials

Article Title: Reduced Order Multiscale Simulation of Diffuse Damage in Concrete

doi: 10.3390/ma14143830

Figure Lengend Snippet: Schematic illustration of the multiscale computational homogenisation approach considered in this paper.

Article Snippet: Mesoscale models can be formulated using a variety of discretisation methods, such as the Finite Element Method (FEM) [ , , , , ], the Discrete Element Method (DEM) [ ], and Fast Fourier Transform (FFT)-based homogenisation methods [ , , ].

Techniques: Homogenization

Material parameters for the large quarzitic aggregates and the calibrated parameters for mortar, containing a volume fraction φ q u a r t z = 30.34 % of fine quarzitic aggregates. The mortar matrix is assumed to contain a 8.3% volume fraction of initial microcracks with an initial aspect ratio of 23. In the investigated concrete sample, the material properties of the mortar matrix with a volume fraction of φ q u a r t z = 43.95 % are determined by varying the volume fraction of aggregate accordingly in the Mori–Tanaka based  homogenisation  procedure, while keeping other parameters unchanged (group Model parameters ). The following sources are used to determine the parameters: [ 1 − 3 ]—Experiment, [ 4 , 5 ] aspect ratio is taken within the range measured in [ <xref ref-type= 69 ], 6 —[ 24 , 70 ]." width="100%" height="100%">

Journal: Materials

Article Title: Reduced Order Multiscale Simulation of Diffuse Damage in Concrete

doi: 10.3390/ma14143830

Figure Lengend Snippet: Material parameters for the large quarzitic aggregates and the calibrated parameters for mortar, containing a volume fraction φ q u a r t z = 30.34 % of fine quarzitic aggregates. The mortar matrix is assumed to contain a 8.3% volume fraction of initial microcracks with an initial aspect ratio of 23. In the investigated concrete sample, the material properties of the mortar matrix with a volume fraction of φ q u a r t z = 43.95 % are determined by varying the volume fraction of aggregate accordingly in the Mori–Tanaka based homogenisation procedure, while keeping other parameters unchanged (group Model parameters ). The following sources are used to determine the parameters: [ 1 − 3 ]—Experiment, [ 4 , 5 ] aspect ratio is taken within the range measured in [ 69 ], 6 —[ 24 , 70 ].

Article Snippet: Mesoscale models can be formulated using a variety of discretisation methods, such as the Finite Element Method (FEM) [ , , , , ], the Discrete Element Method (DEM) [ ], and Fast Fourier Transform (FFT)-based homogenisation methods [ , , ].

Techniques: Homogenization

Schematic illustration of the IDD homogenisation scheme.

Journal: Materials

Article Title: Reduced Order Multiscale Simulation of Diffuse Damage in Concrete

doi: 10.3390/ma14143830

Figure Lengend Snippet: Schematic illustration of the IDD homogenisation scheme.

Article Snippet: Mesoscale models can be formulated using a variety of discretisation methods, such as the Finite Element Method (FEM) [ , , , , ], the Discrete Element Method (DEM) [ ], and Fast Fourier Transform (FFT)-based homogenisation methods [ , , ].

Techniques: Homogenization

Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform (FFT) based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs PIPER energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003

Journal: eLife

Article Title: Encounter complexes and dimensionality reduction in protein–protein association

doi: 10.7554/eLife.01370

Figure Lengend Snippet: Unbound structures were used both for the receptor, EIN (chain A from PDB entry 1ZYM) and for the ligand, HPr (chain P from PDB entry 2JEL). Encounter complexes were generated using Fast Fourier transform (FFT) based sampling. ( A ) Cartoon of the specific complex formed by EIN and HPr, shown in grey and yellow, respectively. The locations of the paramagnetic tags E5C-EDTA-Mn + and E32C-EDTA-Mn 2+ on HPr are encircled and are shown in red and blue, respectively. ( B ) Centers of HPr structures in the encounter complex ensemble. Colors indicate classification as follows ( 8 ): blue, Class I (i.e., overlapping with the specific complex); magenta, patch 1 of Class II (i.e., non-overlapping) positions; red, patch 2 of Class II positions; and pink, additional Class II position outside the main patches. ( C ) Ligand IRMSD vs PIPER energy score. ( D ) Two representative HPr poses, colored light blue and dark blue, from Class I. ( E ) Two representative HPr poses (in different shades of magenta) from Patch 1 of Class II. ( F ) View of the EIN–HPr complex and the centers of HPr poses after rotating 180° around the vertical axis (the bound HPr is now on the left side, almost completely hidden by EIN). ( G ) Representative HPr poses (in different shades of red) from Patch 2 of Class II, shown in the rotated view. DOI: http://dx.doi.org/10.7554/eLife.01370.003

Article Snippet: DB: Owns stock in Acpharis Inc which licensed FFT based sampling program PIPER for commerical use.

Techniques: Generated, Sampling