Modules avx512: Difference between revisions

no edit summary
No edit summary
No edit summary
Line 308: Line 308:
| align="center" | bio
| align="center" | bio
| align="center" | 3.0.4
| align="center" | 3.0.4
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: BayesAss: Bayesian Inference of Recent Migration Using Multilocus Genotypes Homepage: http://www.rannala.org/?page_id=245 URL: http://www.rannala.org/?page_id=245 Keyword:bio<br /><br /><br /></div>
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: BayesAss: Bayesian Inference of Recent Migration Using Multilocus Genotypes Homepage: http://www.rannala.org/?page_id=245 Keyword:bio<br /><br /><br /></div>
|-
|-
| align="center" | [http://www.rannala.org/inference-of-recent-migration bayesass3-snps]
| align="center" | [http://www.rannala.org/inference-of-recent-migration bayesass3-snps]
Line 388: Line 388:
| align="center" | -
| align="center" | -
| align="center" | 1.03
| align="center" | 1.03
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: bgc implements Bayesian estimation of genomic clines to quantify introgression at many loci. Models are available for linked loci, genotype uncertainty and sequence errors. Models for genotype uncertainty and sequence error can be used to estimate genomic cline parameters from next-generation sequence data. Homepage: https://sites.google.com/site/bgcsoftware/<br /><br /><br /></div>
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: bgc implements Bayesian estimation of genomic clines to quantify introgression at many loci. Models are available for linked loci, genotype uncertainty and sequence errors. Models for genotype uncertainty and sequence error can be used to estimate genomic cline parameters from next-generation sequence data. Homepage: https://sites.google.com/site/bgcsoftware/ URL: https://sites.google.com/site/bgcsoftware/<br /><br /><br /></div>
|-
|-
| align="center" | [https://bitbucket.org/gavinband/bgen/src/default/ bgen]
| align="center" | [https://bitbucket.org/gavinband/bgen/src/default/ bgen]
Line 1,743: Line 1,743:
| align="center" | -
| align="center" | -
| align="center" | 3.3.2, 3.3.8
| align="center" | 3.3.2, 3.3.8
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: GLFW is an Open Source, multi-platform library for OpenGL, OpenGL ES and Vulkan development on the desktop Homepage: https://www.glfw.org URL: https://www.glfw.org<br /><br /><br /></div>
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: GLFW is an Open Source, multi-platform library for OpenGL, OpenGL ES and Vulkan development on the desktop Homepage: https://www.glfw.org URL: https://www.glfw.org Compatible modules: python/3.10, python/3.10, python/3.10, python/3.10, python/3.11, python/3.11, python/3.11, python/3.11 Extensions: glfw-2.6.2<br /><br /><br /></div>
|-
|-
| align="center" | [https://ccb.jhu.edu/software/glimmerhmm glimmerhmm]
| align="center" | [https://ccb.jhu.edu/software/glimmerhmm glimmerhmm]
Line 1,848: Line 1,848:
| align="center" | vis
| align="center" | vis
| align="center" | 5.99.0
| align="center" | 5.99.0
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: Grace is a WYSIWYG 2D plotting tool for X Windows System and Motif. Homepage: http://freecode.com/projects/grace Keyword:vis<br /><br /><br /></div>
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: Grace is a WYSIWYG 2D plotting tool for X Windows System and Motif. Homepage: http://freecode.com/projects/grace URL: http://freecode.com/projects/grace Keyword:vis<br /><br /><br /></div>
|-
|-
| align="center" | [http://grackle.readthedocs.io grackle]
| align="center" | [http://grackle.readthedocs.io grackle]
Line 2,847: Line 2,847:
| align="center" | [https://sourceforge.net/projects/matio/ matio]
| align="center" | [https://sourceforge.net/projects/matio/ matio]
| align="center" | io
| align="center" | io
| align="center" | 1.5.19, 1.5.26
| align="center" | 1.5.2, 1.5.19, 1.5.26
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: matio is an C library for reading and writing Matlab MAT files. Homepage: https://sourceforge.net/projects/matio/ URL: https://sourceforge.net/projects/matio/ Keyword:io<br /><br /><br /></div>
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: matio is an C library for reading and writing Matlab MAT files. Homepage: https://sourceforge.net/projects/matio/ URL: https://sourceforge.net/projects/matio/ Keyword:io<br /><br /><br /></div>
|-
|-
Line 3,013: Line 3,013:
| align="center" | bio
| align="center" | bio
| align="center" | 2.0.1
| align="center" | 2.0.1
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: Minimac3 is a lower memory and more computationally efficient implementation of the genotype imputation algorithms in minimac and minimac2. Minimac3 is designed to handle very large reference panels in a more computationally efficient way with no loss of accuracy. Homepage: http://genome.sph.umich.edu/wiki/Minimac3 URL: http://genome.sph.umich.edu/wiki/Minimac3 Keyword:bio<br /><br /><br /></div>
| <div class="mw-collapsible mw-collapsed" style="white-space: pre-line;"><br />Description: Minimac3 is a lower memory and more computationally efficient implementation of the genotype imputation algorithms in minimac and minimac2. Minimac3 is designed to handle very large reference panels in a more computationally efficient way with no loss of accuracy. Homepage: http://genome.sph.umich.edu/wiki/Minimac3 Keyword:bio<br /><br /><br /></div>
|-
|-
| align="center" | [https://genome.sph.umich.edu/wiki/Minimac4 minimac4]
| align="center" | [https://genome.sph.umich.edu/wiki/Minimac4 minimac4]
cc_staff
153

edits