roebe 0.5.122

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Files changed (2730) hide show
  1. checksums.yaml +7 -0
  2. data/README.md +2596 -0
  3. data/bin/blinking_cursor +7 -0
  4. data/bin/browser +7 -0
  5. data/bin/colourized_tokenitor1 +7 -0
  6. data/bin/colourized_tokenitor2 +7 -0
  7. data/bin/colourized_tokenitor3 +7 -0
  8. data/bin/colourized_tokenitor4 +7 -0
  9. data/bin/colourized_tokenitor5 +7 -0
  10. data/bin/compare_these_two_directories +7 -0
  11. data/bin/create_file_skeleton +7 -0
  12. data/bin/create_my_directories +7 -0
  13. data/bin/create_zip +7 -0
  14. data/bin/display_gcc_version +7 -0
  15. data/bin/do_a_google_search +7 -0
  16. data/bin/extract_gem_file +7 -0
  17. data/bin/fragment_maker +7 -0
  18. data/bin/generate_fstab_file +7 -0
  19. data/bin/hello_world +7 -0
  20. data/bin/in +7 -0
  21. data/bin/increment_application_version +7 -0
  22. data/bin/increment_application_version_then_push_the_gem +13 -0
  23. data/bin/install_all_registered_fonts +7 -0
  24. data/bin/install_my_addons +115 -0
  25. data/bin/interactive_file_creator +7 -0
  26. data/bin/kill_firefox +7 -0
  27. data/bin/kill_palemoon +7 -0
  28. data/bin/konsole_title +7 -0
  29. data/bin/larrow +7 -0
  30. data/bin/log10 +7 -0
  31. data/bin/menugenerator +7 -0
  32. data/bin/openpdf1 +7 -0
  33. data/bin/openpdf2 +7 -0
  34. data/bin/openpdf3 +7 -0
  35. data/bin/openpdf4 +7 -0
  36. data/bin/openpdf5 +7 -0
  37. data/bin/openpdf6 +7 -0
  38. data/bin/openpdf7 +7 -0
  39. data/bin/openpdf8 +7 -0
  40. data/bin/openpdf9 +7 -0
  41. data/bin/passwords +7 -0
  42. data/bin/path_generator +7 -0
  43. data/bin/print_this_unicode_symbol +7 -0
  44. data/bin/quick_colour_test +13 -0
  45. data/bin/rarrow +7 -0
  46. data/bin/rdate +7 -0
  47. data/bin/remove_this_substring_from_all_files +7 -0
  48. data/bin/replace_space_with_underscore +7 -0
  49. data/bin/rfirefox +7 -0
  50. data/bin/rinstall2 +7 -0
  51. data/bin/roebe +7 -0
  52. data/bin/roebe_documentation +7 -0
  53. data/bin/roebeshell +11 -0
  54. data/bin/ruby_cat +7 -0
  55. data/bin/ruby_dhcpcd +7 -0
  56. data/bin/run +7 -0
  57. data/bin/rxinitrc +7 -0
  58. data/bin/set_alias_1 +7 -0
  59. data/bin/set_alias_10 +7 -0
  60. data/bin/set_alias_2 +7 -0
  61. data/bin/set_alias_3 +7 -0
  62. data/bin/set_alias_4 +7 -0
  63. data/bin/set_alias_5 +7 -0
  64. data/bin/set_alias_6 +7 -0
  65. data/bin/set_alias_7 +7 -0
  66. data/bin/set_alias_8 +7 -0
  67. data/bin/set_alias_9 +7 -0
  68. data/bin/set_browser +7 -0
  69. data/bin/setpdf1 +7 -0
  70. data/bin/setpdf2 +7 -0
  71. data/bin/setpdf3 +7 -0
  72. data/bin/setpdf4 +7 -0
  73. data/bin/setpdf5 +7 -0
  74. data/bin/setpdf6 +7 -0
  75. data/bin/setpdf7 +7 -0
  76. data/bin/setpdf8 +7 -0
  77. data/bin/setpdf9 +7 -0
  78. data/bin/show_available_users +7 -0
  79. data/bin/show_ten_aliases +7 -0
  80. data/bin/simple_extractor +9 -0
  81. data/bin/symlink_directories_from_that_directory_to_the_current_directory +7 -0
  82. data/bin/symlink_everything_from_that_directory_to_this_directory +7 -0
  83. data/bin/symlink_files_from_that_directory_to_the_current_directory +7 -0
  84. data/bin/take_screenshot +7 -0
  85. data/bin/to_binary +7 -0
  86. data/bin/tokenitor +7 -0
  87. data/bin/trad +7 -0
  88. data/bin/vim_paradise +7 -0
  89. data/bin/wlan +7 -0
  90. data/doc/CONFIGURATION_FOR_THE_ROEBE_SHELL.md +381 -0
  91. data/doc/MANIFESTO_FOR_THE_ROEBE_SHELL_COMPONENT.md +391 -0
  92. data/doc/PHILOSOPHY_OF_THE_ROEBE_SHELL.md +64 -0
  93. data/doc/README.gen +2553 -0
  94. data/doc/add_ons_for_ruby/README.md +3 -0
  95. data/doc/add_ons_for_ruby/axlsx.md +60 -0
  96. data/doc/add_ons_for_ruby/fxruby.md +14 -0
  97. data/doc/add_ons_for_ruby/glimmer-libui.md +44 -0
  98. data/doc/add_ons_for_ruby/jruby.md +132 -0
  99. data/doc/add_ons_for_ruby/opal.md +34 -0
  100. data/doc/add_ons_for_ruby/prawn.md +12 -0
  101. data/doc/add_ons_for_ruby/sequel.md +51 -0
  102. data/doc/core/array.md +11 -0
  103. data/doc/deprecations.md +10 -0
  104. data/doc/diamond_shell_tutorial.cgi +2924 -0
  105. data/doc/linux_may_have_issues.md +92 -0
  106. data/doc/misc/how_to_publish.md +49 -0
  107. data/doc/misc/the_perfect_book.md +14 -0
  108. data/doc/ruby_on_rails_tutorial/data_types_for_rails_migrations.md +11 -0
  109. data/doc/ruby_on_rails_tutorial/ruby_on_rails_tutorial.cgi +404 -0
  110. data/doc/sinatra_tutorial/sinatra_tutorial.cgi +7 -0
  111. data/doc/sinatra_tutorial/sinatra_tutorial.rb +930 -0
  112. data/doc/sinatra_tutorial/sinatra_tutorial.sinatra +56 -0
  113. data/doc/statistics/statistics.md +94 -0
  114. data/doc/todo/todo_for_the_roebe_project.md +1 -0
  115. data/doc/todo/todo_for_the_roebe_project_on_windows.md +8 -0
  116. data/doc/todo/todo_for_the_roebe_shell.md +1178 -0
  117. data/examples/rmagick/001_axes.rb +68 -0
  118. data/examples/rmagick/002_basic_2D_canvas.rb +29 -0
  119. data/examples/rmagick/003_a_walking_duck.rb +42 -0
  120. data/examples/rmagick/004_black_rectangle_with_red_border.rb +37 -0
  121. data/examples/rmagick/A_WALKING_DUCK.gif +0 -0
  122. data/examples/rmagick/foobar.png +0 -0
  123. data/lib/roebe/autoinclude.rb +4 -0
  124. data/lib/roebe/autoinclude_encoding.rb +11 -0
  125. data/lib/roebe/autoinclude_open.rb +3 -0
  126. data/lib/roebe/base/base.rb +25 -0
  127. data/lib/roebe/base/chdir.rb +43 -0
  128. data/lib/roebe/base/colours.rb +539 -0
  129. data/lib/roebe/base/commandline_arguments.rb +86 -0
  130. data/lib/roebe/base/constants.rb +25 -0
  131. data/lib/roebe/base/copy.rb +70 -0
  132. data/lib/roebe/base/editor.rb +18 -0
  133. data/lib/roebe/base/encoding.rb +54 -0
  134. data/lib/roebe/base/env.rb +22 -0
  135. data/lib/roebe/base/esystem.rb +84 -0
  136. data/lib/roebe/base/home_directory_of_user_x.rb +27 -0
  137. data/lib/roebe/base/is_on_roebe.rb +22 -0
  138. data/lib/roebe/base/misc.rb +357 -0
  139. data/lib/roebe/base/next.rb +29 -0
  140. data/lib/roebe/base/opnn.rb +46 -0
  141. data/lib/roebe/base/prototype.rb +409 -0
  142. data/lib/roebe/base/reset.rb +37 -0
  143. data/lib/roebe/base/run.rb +17 -0
  144. data/lib/roebe/base/simp.rb +25 -0
  145. data/lib/roebe/base/support_for_beautiful_url.rb +28 -0
  146. data/lib/roebe/base/symlink.rb +51 -0
  147. data/lib/roebe/base/time.rb +165 -0
  148. data/lib/roebe/base/verbose_truth.rb +21 -0
  149. data/lib/roebe/base/write_what_into.rb +33 -0
  150. data/lib/roebe/browser/README.md +5 -0
  151. data/lib/roebe/browser/browser.rb +26 -0
  152. data/lib/roebe/browser/constants.rb +43 -0
  153. data/lib/roebe/browser/firefox.rb +51 -0
  154. data/lib/roebe/browser/menu.rb +103 -0
  155. data/lib/roebe/browser/misc.rb +367 -0
  156. data/lib/roebe/browser/output_url_then_open_in_browser.rb +168 -0
  157. data/lib/roebe/browser/palemoon.rb +59 -0
  158. data/lib/roebe/browser/reset.rb +50 -0
  159. data/lib/roebe/cat/cat.rb +137 -0
  160. data/lib/roebe/cat/method.rb +14 -0
  161. data/lib/roebe/classes/add_irc_quote.rb +132 -0
  162. data/lib/roebe/classes/add_newline_after.rb +124 -0
  163. data/lib/roebe/classes/add_this_user_to_the_sudoers_file.rb +67 -0
  164. data/lib/roebe/classes/add_user_lighty.rb +104 -0
  165. data/lib/roebe/classes/aggregate_all_files_together_from_this_directory.rb +86 -0
  166. data/lib/roebe/classes/aliases.rb +683 -0
  167. data/lib/roebe/classes/all_games.rb +61 -0
  168. data/lib/roebe/classes/all_my_gems.rb +101 -0
  169. data/lib/roebe/classes/alphabetical_sorter.rb +117 -0
  170. data/lib/roebe/classes/apache_configuration_maker.rb +234 -0
  171. data/lib/roebe/classes/append_this.rb +156 -0
  172. data/lib/roebe/classes/append_to_line.rb +141 -0
  173. data/lib/roebe/classes/ascii/README.md +2 -0
  174. data/lib/roebe/classes/ascii/fix_missing_numbers_for_ascii_paradise.rb +96 -0
  175. data/lib/roebe/classes/at.rb +300 -0
  176. data/lib/roebe/classes/automounter.rb +181 -0
  177. data/lib/roebe/classes/available_classes.rb +219 -0
  178. data/lib/roebe/classes/backup_core_system.rb +223 -0
  179. data/lib/roebe/classes/basic_configure.rb +110 -0
  180. data/lib/roebe/classes/batch_generate_all_my_gems.rb +132 -0
  181. data/lib/roebe/classes/become_another_user.rb +86 -0
  182. data/lib/roebe/classes/bezirk.rb +91 -0
  183. data/lib/roebe/classes/birthday_notifications.rb +291 -0
  184. data/lib/roebe/classes/burn_iso/burn_iso.rb +274 -0
  185. data/lib/roebe/classes/burn_iso/constants.rb +43 -0
  186. data/lib/roebe/classes/burn_iso/initialize.rb +33 -0
  187. data/lib/roebe/classes/caesar_cipher.rb +88 -0
  188. data/lib/roebe/classes/calendar.rb +360 -0
  189. data/lib/roebe/classes/calendar_maker.rb +61 -0
  190. data/lib/roebe/classes/celsius_to_fahrenheit.rb +195 -0
  191. data/lib/roebe/classes/check_for_bad_blocks.rb +67 -0
  192. data/lib/roebe/classes/check_yaml.rb +71 -0
  193. data/lib/roebe/classes/chmod_current_time.rb +71 -0
  194. data/lib/roebe/classes/clipboard.rb +221 -0
  195. data/lib/roebe/classes/clock.rb +118 -0
  196. data/lib/roebe/classes/compare_these_two_directories.rb +95 -0
  197. data/lib/roebe/classes/compare_these_two_files.rb +167 -0
  198. data/lib/roebe/classes/compile_kernel.rb +114 -0
  199. data/lib/roebe/classes/config_generator.rb +204 -0
  200. data/lib/roebe/classes/conky.rb +121 -0
  201. data/lib/roebe/classes/conky_rcfile_generator.rb +61 -0
  202. data/lib/roebe/classes/convert_encoding_of_this_file.rb +215 -0
  203. data/lib/roebe/classes/convert_file_into_utf_encoding.rb +89 -0
  204. data/lib/roebe/classes/convert_this_cgi_file_into_a_sinatrafied_application.rb +145 -0
  205. data/lib/roebe/classes/copy_from_glibc.rb +134 -0
  206. data/lib/roebe/classes/copy_here.rb +76 -0
  207. data/lib/roebe/classes/copy_kernel_config.rb +59 -0
  208. data/lib/roebe/classes/copy_these_directories_to.rb +121 -0
  209. data/lib/roebe/classes/covid_lethality.rb +243 -0
  210. data/lib/roebe/classes/create_asoundrc_file.rb +66 -0
  211. data/lib/roebe/classes/create_benchmark_file.rb +77 -0
  212. data/lib/roebe/classes/create_desktop_file.rb +236 -0
  213. data/lib/roebe/classes/create_docbook_sgml_dtd_catalog.rb +113 -0
  214. data/lib/roebe/classes/create_file_skeleton/constants.rb +70 -0
  215. data/lib/roebe/classes/create_file_skeleton/create_file_skeleton.rb +470 -0
  216. data/lib/roebe/classes/create_file_skeleton/generate_c_string.rb +31 -0
  217. data/lib/roebe/classes/create_file_skeleton/generate_cpp_string.rb +33 -0
  218. data/lib/roebe/classes/create_file_skeleton/generate_ruby_string.rb +124 -0
  219. data/lib/roebe/classes/create_file_skeleton/reset.rb +56 -0
  220. data/lib/roebe/classes/create_file_skeleton/run.rb +23 -0
  221. data/lib/roebe/classes/create_firefox_extension.rb +186 -0
  222. data/lib/roebe/classes/create_iso.rb +203 -0
  223. data/lib/roebe/classes/create_iso_for_games.rb +308 -0
  224. data/lib/roebe/classes/create_jar_archive.rb +58 -0
  225. data/lib/roebe/classes/create_my_directories.rb +216 -0
  226. data/lib/roebe/classes/create_ruby_directory_layout.rb +125 -0
  227. data/lib/roebe/classes/create_zip.rb +112 -0
  228. data/lib/roebe/classes/css_analyzer.rb +125 -0
  229. data/lib/roebe/classes/current_monitor_resolution.rb +107 -0
  230. data/lib/roebe/classes/custom_table/custom_table.rb +198 -0
  231. data/lib/roebe/classes/daemonize.rb +131 -0
  232. data/lib/roebe/classes/date_sort.rb +149 -0
  233. data/lib/roebe/classes/day_calendar.rb +153 -0
  234. data/lib/roebe/classes/dbus.rb +132 -0
  235. data/lib/roebe/classes/delete_all_directories.rb +100 -0
  236. data/lib/roebe/classes/delete_empty_directories.rb +96 -0
  237. data/lib/roebe/classes/delete_empty_files.rb +142 -0
  238. data/lib/roebe/classes/dhcpcd.rb +125 -0
  239. data/lib/roebe/classes/differences_between_two_directories.rb +140 -0
  240. data/lib/roebe/classes/disable.rb +138 -0
  241. data/lib/roebe/classes/display_gcc_version.rb +135 -0
  242. data/lib/roebe/classes/do_a_google_search.rb +67 -0
  243. data/lib/roebe/classes/do_install.rb +233 -0
  244. data/lib/roebe/classes/done.rb +158 -0
  245. data/lib/roebe/classes/done_and_open.rb +183 -0
  246. data/lib/roebe/classes/doskey_generator.rb +198 -0
  247. data/lib/roebe/classes/downcase_directories.rb +83 -0
  248. data/lib/roebe/classes/downcase_extension.rb +136 -0
  249. data/lib/roebe/classes/download_from_this_url.rb +266 -0
  250. data/lib/roebe/classes/email.rb +635 -0
  251. data/lib/roebe/classes/enable.rb +59 -0
  252. data/lib/roebe/classes/enable_autologin.rb +378 -0
  253. data/lib/roebe/classes/english_to_german.rb +128 -0
  254. data/lib/roebe/classes/ethernet.rb +171 -0
  255. data/lib/roebe/classes/euclidian_distance.rb +148 -0
  256. data/lib/roebe/classes/extract_gem_file.rb +208 -0
  257. data/lib/roebe/classes/feet_to_centimetres.rb +106 -0
  258. data/lib/roebe/classes/fetch_random_line.rb +66 -0
  259. data/lib/roebe/classes/fetch_url.rb +77 -0
  260. data/lib/roebe/classes/file_parser.rb +126 -0
  261. data/lib/roebe/classes/file_renamer.rb +229 -0
  262. data/lib/roebe/classes/files_that_could_become_apps.rb +95 -0
  263. data/lib/roebe/classes/filter_apache_log.rb +90 -0
  264. data/lib/roebe/classes/find_all_files_encoded_in_iso.rb +99 -0
  265. data/lib/roebe/classes/find_all_files_with_a_question_mark.rb +148 -0
  266. data/lib/roebe/classes/find_duplicate_entries_in_alias_file.rb +168 -0
  267. data/lib/roebe/classes/find_empty_files.rb +88 -0
  268. data/lib/roebe/classes/find_expanded_alias.rb +267 -0
  269. data/lib/roebe/classes/find_out_version_of.rb +193 -0
  270. data/lib/roebe/classes/find_static_libraries.rb +220 -0
  271. data/lib/roebe/classes/fix_mcookie.rb +84 -0
  272. data/lib/roebe/classes/fix_timezone.rb +95 -0
  273. data/lib/roebe/classes/fluxbox/README.md +3 -0
  274. data/lib/roebe/classes/fluxbox/autogenerate_fluxbox_files.rb +20 -0
  275. data/lib/roebe/classes/fluxbox/generate_fluxbox_apps_file.rb +155 -0
  276. data/lib/roebe/classes/fluxbox/generate_fluxbox_keys_file.rb +110 -0
  277. data/lib/roebe/classes/fluxbox/install_fluxbox_style.rb +85 -0
  278. data/lib/roebe/classes/font_installer.rb +119 -0
  279. data/lib/roebe/classes/fotos_f/303/274r_ingrid.rb +50 -0
  280. data/lib/roebe/classes/fragment_maker.rb +141 -0
  281. data/lib/roebe/classes/general_overviewer.rb +258 -0
  282. data/lib/roebe/classes/generate_alsa_conf.rb +108 -0
  283. data/lib/roebe/classes/generate_etc_resolv_conf_file.rb +106 -0
  284. data/lib/roebe/classes/generate_fstab_file/generate_fstab_file.rb +255 -0
  285. data/lib/roebe/classes/generate_gemspec/constants.rb +58 -0
  286. data/lib/roebe/classes/generate_gemspec/generate_gemspec.rb +195 -0
  287. data/lib/roebe/classes/generate_locales.rb +114 -0
  288. data/lib/roebe/classes/generate_ls_colors.rb +92 -0
  289. data/lib/roebe/classes/generate_master_shell_script.rb +254 -0
  290. data/lib/roebe/classes/generate_nsswitch_conf.rb +110 -0
  291. data/lib/roebe/classes/generate_overview_of_the_locally_available_books.rb +178 -0
  292. data/lib/roebe/classes/generate_protocols.rb +253 -0
  293. data/lib/roebe/classes/generate_rewrite_rules.rb +266 -0
  294. data/lib/roebe/classes/generate_robots_txt_file.rb +104 -0
  295. data/lib/roebe/classes/generate_rtf_file.rb +132 -0
  296. data/lib/roebe/classes/generate_system_values.rb +164 -0
  297. data/lib/roebe/classes/generate_unit_files/README.md +9 -0
  298. data/lib/roebe/classes/generate_unit_files/generate_unit_files.rb +192 -0
  299. data/lib/roebe/classes/generate_xauthority_file.rb +119 -0
  300. data/lib/roebe/classes/generate_xorg_conf/constants.rb +145 -0
  301. data/lib/roebe/classes/generate_xorg_conf/generate_xorg_conf.rb +767 -0
  302. data/lib/roebe/classes/get_dependencies.rb +175 -0
  303. data/lib/roebe/classes/good_night.rb +72 -0
  304. data/lib/roebe/classes/google_url_cleaner.rb +147 -0
  305. data/lib/roebe/classes/grant_superuser_rights.rb +146 -0
  306. data/lib/roebe/classes/grub/grub_config_generator.rb +184 -0
  307. data/lib/roebe/classes/grub_appender.rb +246 -0
  308. data/lib/roebe/classes/gzip_this_file.rb +86 -0
  309. data/lib/roebe/classes/hello_world.rb +60 -0
  310. data/lib/roebe/classes/hex_to_rgb.rb +89 -0
  311. data/lib/roebe/classes/holiday.rb +99 -0
  312. data/lib/roebe/classes/hosts_appender.rb +171 -0
  313. data/lib/roebe/classes/html_form_fetcher.rb +101 -0
  314. data/lib/roebe/classes/icewm/README.md +3 -0
  315. data/lib/roebe/classes/icewm/icewm_keys_generator.rb +162 -0
  316. data/lib/roebe/classes/identical.rb +174 -0
  317. data/lib/roebe/classes/imdb.rb +86 -0
  318. data/lib/roebe/classes/in.rb +156 -0
  319. data/lib/roebe/classes/increment_application_version.rb +291 -0
  320. data/lib/roebe/classes/inhalt.rb +166 -0
  321. data/lib/roebe/classes/inputrc/constants.rb +37 -0
  322. data/lib/roebe/classes/inputrc/inputrc.rb +567 -0
  323. data/lib/roebe/classes/inputrc/misc.rb +11 -0
  324. data/lib/roebe/classes/install_debian_file.rb +172 -0
  325. data/lib/roebe/classes/install_flash/install_flash.rb +179 -0
  326. data/lib/roebe/classes/install_libreoffice/constants.rb +39 -0
  327. data/lib/roebe/classes/install_libreoffice/install_libreoffice.rb +232 -0
  328. data/lib/roebe/classes/install_my_gems.rb +100 -0
  329. data/lib/roebe/classes/install_openssl_certificates.rb +238 -0
  330. data/lib/roebe/classes/install_ruby_project.rb +180 -0
  331. data/lib/roebe/classes/interactive_file_creator.rb +229 -0
  332. data/lib/roebe/classes/into.rb +95 -0
  333. data/lib/roebe/classes/ipaste.rb +88 -0
  334. data/lib/roebe/classes/iso_to_usb.rb +239 -0
  335. data/lib/roebe/classes/java_header.rb +112 -0
  336. data/lib/roebe/classes/kde/install_this_konsole_theme.rb +87 -0
  337. data/lib/roebe/classes/kde/kde_konsole/constants.rb +54 -0
  338. data/lib/roebe/classes/kde/kde_konsole/help.rb +33 -0
  339. data/lib/roebe/classes/kde/kde_konsole/initialize.rb +40 -0
  340. data/lib/roebe/classes/kde/kde_konsole/kde_konsole.rb +37 -0
  341. data/lib/roebe/classes/kde/kde_konsole/menu.rb +200 -0
  342. data/lib/roebe/classes/kde/kde_konsole/misc.rb +333 -0
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  2702. data/test/misc/fetch_a_specific_key_from_a_hash.rb +26 -0
  2703. data/test/misc/fork_example.rb +15 -0
  2704. data/test/misc/hello_world.rb +1 -0
  2705. data/test/misc/heredoc_example.rb +9 -0
  2706. data/test/misc/minimal_irc_bot/minimal_irc_bot.rb +33 -0
  2707. data/test/misc/name_of_this_script.rb +12 -0
  2708. data/test/misc/read_keypresses.rb +79 -0
  2709. data/test/misc/readline/README.md +1 -0
  2710. data/test/misc/readline/completion_for_a_static_list.rb +33 -0
  2711. data/test/misc/simple_sigint_example.rb +51 -0
  2712. data/test/misc/simple_user_input_via_stdin_or_Readline_example.rb +14 -0
  2713. data/test/misc/tcp_socket_example.rb +28 -0
  2714. data/test/misc/tracer.rb +39 -0
  2715. data/test/misc/with_border.rb +22 -0
  2716. data/test/testing_cat.rb +3 -0
  2717. data/test/testing_class_configuration/testing_class_configuration.rb +81 -0
  2718. data/test/testing_core_functionality_of_ruby/README.md +6 -0
  2719. data/test/testing_core_functionality_of_ruby/file_test.rb +1 -0
  2720. data/test/testing_core_functionality_of_ruby/verbose_file_copy.rb +5 -0
  2721. data/test/testing_google_url_cleaner.rb +25 -0
  2722. data/test/testing_http_status_codes.rb +13 -0
  2723. data/test/testing_identical.rb +17 -0
  2724. data/test/testing_move_file.rb +14 -0
  2725. data/test/testing_permission_ascii_format.rb +23 -0
  2726. data/test/testing_sql_paradise.rb +17 -0
  2727. data/test/testing_the_roebe_shell.rb +31 -0
  2728. data/test/testing_twentyfour_hours_notation.rb +37 -0
  2729. data/test/testing_zenity.rb +26 -0
  2730. metadata +2873 -0
@@ -0,0 +1,1115 @@
1
+ english(:filename) {
2
+ autoextend
3
+ template1 '
4
+
5
+ a { text-decoration: none; color: steelblue; }
6
+ a:link { text-decoration: none; color: steelblue; }
7
+ a:hover { text-decoration: none; color: royalblue; }
8
+
9
+ p.default {
10
+ margin: 4px;
11
+ margin-left: 1em;
12
+ margin-right: 1em;
13
+ padding: 5px;
14
+ }
15
+
16
+ '
17
+ ruby_favicon
18
+ body_css_class 's12px padt4px marpad2px VERDANAs'
19
+ body_css_style 'background-color: #d3d2d1;'
20
+ font_size 'def'
21
+
22
+ # =========================================================================== #
23
+ # === header
24
+ # =========================================================================== #
25
+ def header(
26
+ i = '',
27
+ optional_css_class = ''
28
+ )
29
+ h2 i, optional_css_class
30
+ end
31
+
32
+ doc {
33
+ dimg2 'science/genetics/DNA_HELIX_UND_RATTE.png',
34
+ 'https://i.imgur.com/tHpLvvL.jpg',
35
+ 'bblack3 mars0_5em'
36
+ br
37
+ # ========================================================================= #
38
+ # === Tabelle der Nukleoside
39
+ # ========================================================================= #
40
+ h2 'Tabelle der Nukleoside'
41
+ br
42
+ table2('mars2em larger BOLD','','',
43
+ 'Basen:','Nukleoside:',
44
+ 'Adenin ←','→ Adenosin',
45
+ 'Guanin ←','→ Guanosin',
46
+ 'Thymin ←','→ Thymidin',
47
+ 'Cytosin ←','→ Cytidin',
48
+ 'Uracil ←','→ Uridin'
49
+ )
50
+ pretty_hsep
51
+ header 'Sigma-Faktoren','mart1px marb10px'
52
+ p_default {
53
+ e 'Sigma 32 bei E.coli erkennt eine andere Sequenz als (Standard)
54
+ Sigma 70. Ich tausche einen Teil der Polymerase aus - und schon
55
+ funktioniert sie komplett anders!'
56
+ }
57
+ pretty_hsep
58
+ # ========================================================================= #
59
+ # === Nomenklatur von Genen
60
+ # ========================================================================= #
61
+ header 'Nomenklatur der Gene'
62
+ div('default martb1px') {
63
+ p('marb1px') {
64
+ e 'Die verschiedenen <b>Namen</b> für Gene entstammen oft der
65
+ Geschichte ihrer Entdeckung - sprich, wann, wie und von welcher
66
+ Person oder von welchen Personen sie entdeckt wurden:'
67
+ br
68
+ lem2 '- Ein Zellbiologie gibt den Namen anhand der zellulären Funktion.'
69
+ br
70
+ lem2 '- Ein Entwicklungsbiologe anhand von Mutanten die defekt sind.'
71
+ }
72
+ }
73
+ # ========================================================================= #
74
+ # === ESTs
75
+ # ========================================================================= #
76
+ h2 'ESTs'
77
+ div {
78
+ p {
79
+ e '<b>ESTs</b> (aka <b>expressed sequence tags</b> are short sequences
80
+ derived from messenger RNAs. These can, in turn, be hybridized to
81
+ chromosomal DNA. The advantage of this was that this allowed
82
+ scientists in the 1990s to easily identify open reading frames.'
83
+ }
84
+ }
85
+ # ========================================================================= #
86
+ # === Historische Fakten tag
87
+ # ========================================================================= #
88
+ h2 'Historische und kuriose Fakten'
89
+ div_default {
90
+ p_default {
91
+ e 'Im Jahre <b>1970</b> sequenzierte <b>Ray Wu</b> als erster ein DNA
92
+ Fragment - zwölf Basen am Ende eines Einzelstrangs entstanden aus
93
+ einem durch Enzyme geschnittenen Ring.'
94
+ }
95
+ }
96
+ # ========================================================================= #
97
+ # === DNA Microarrays tag
98
+ # ========================================================================= #
99
+ header 'DNA Microarrays','mart1px'
100
+ div('default ind0 wid95 mart2px','dna_microarrays'){
101
+ e '<b>DNA Microarrays</b> make it possible to create a global profile
102
+ of all expressed RNA within a cell or cell homogenisate.'
103
+ br
104
+ e 'This pattern that will be capture is often very characteristic
105
+ of the given cell or tissue, which in turn allows characterization
106
+ of disease patterns (in theory).'
107
+ br
108
+ dimg 'science/DNA_MICROARRAY.png',
109
+ 'mars3em'
110
+ }
111
+ # ========================================================================= #
112
+ # === MITOCHONDRIUM
113
+ # ========================================================================= #
114
+ div(id: 'mitochondrium'){
115
+ h4 'Mitochondrium'
116
+ dimg 'science/biology/organelles/MITOCHONDRIUM_OVERVIEW.png',
117
+ 'bblack3 marl1em'
118
+ dimg 'science/biology/organelles/TEM_Bild_eines_Mitochondriums.png',
119
+ 'bblack3'
120
+ }
121
+ # ========================================================================= #
122
+ # === Thymidylat-Synthase Tag. dUMP -> dTMP
123
+ # ========================================================================= #
124
+ div {
125
+ h2 'Thymidylat-Synthase'
126
+ p {
127
+ e 'dUMP wird durch <b>Thymidylat-Synthase</b> in dTMP umgewandelt,
128
+ indem eine Methylgruppe angeheftet wird.'
129
+ }
130
+ }
131
+ # =========================================================================== #
132
+ # === misc tag tidbits tag
133
+ # =========================================================================== #
134
+ div {
135
+ e 'Helikasen wurden im Jahre 1976 durch <b>Hoffman-Berling</b> entdeckt.'
136
+ br
137
+ e 'SSB ist auch insofern wichtig, da es <b>secondary structures</b>
138
+ reduziert.'
139
+ br
140
+ e '<b>RecA</b> wird durch ATP "angeregt", die Affinität zu DNA
141
+ steigt.'
142
+ br
143
+ e 'Die <b>Shine-Dalgarno Sequenz</b> auf der mRNA ist AGG-AGG-U'
144
+ br
145
+ e 'Wo natürlicherweise Kalkstein auftritt, ist der Boden weniger sauer.'
146
+ }
147
+ # ========================================================================= #
148
+ # === Gene Map Viewer
149
+ # ========================================================================= #
150
+ header 'Gene Map Viewers (Ensembl and others)'
151
+ div('ind0 wid95 mart2px'){
152
+ e 'The Ensemble Gene Map Viewer contains entries for humans,
153
+ chicken, fugu, fruitfly and many other organisms.'
154
+ br
155
+ abr 'https://www.ensembl.org/index.html',
156
+ content: 'Ensembl Gene Map Viewer - Show different Animals '\
157
+ 'and Human Genomes',
158
+ css_class: 'BOLD mars1em'
159
+ br
160
+ e 'The above Ensembl Application has been written in perl.'
161
+ br
162
+ e 'Especially these reviews may be helpful for anyone curious
163
+ to find out more about it:'
164
+ br
165
+ e 'James Stalker et al. The Ensembl Web Site: Mechanics of
166
+ a Genome Browser Genome Res. 2004 14: 951-955.'
167
+ br
168
+ e 'It can be found here:'
169
+ br
170
+ abr 'https://www.genome.org/cgi/content/abstract/14/5/951',
171
+ content: 'Review of the GeneMap Viewer',
172
+ css_class: 'BOLD mars1em'
173
+ abr 'https://www.ensembl.org/Docs/',
174
+ content: 'Good Documents for Ensembl',
175
+ css_class: 'BOLD mars1em'
176
+ }
177
+ # ========================================================================= #
178
+ # === Die Terminale Transferase
179
+ # ========================================================================= #
180
+ header 'Die Terminale Transferase'
181
+ div {
182
+ lembre '<b>Terminale Tranferase</b> katalysiert die Addition von
183
+ Nukleotiden an das <b>3-Strich Ende von DNA</b>.'
184
+ lembre "Interessanterweise arbeitet dieses Enzym an ssDNA und benötigt
185
+ keinen Primer. Es scheint auch Ribonucleotide an die 3' Enden von DNA
186
+ hinzufügen zu können."
187
+ lembre 'Cobalt ist ein Kofaktor dieses Enzyms.'
188
+ }
189
+ # ========================================================================= #
190
+ # === Cosuppression tag (ist NICHT Codominance!)
191
+ # ========================================================================= #
192
+ header 'Cosuppression'
193
+ div {
194
+ e '<b>Cosuppression</b> ist dann zu beobachten wenn sowohl das
195
+ <b>Transgen</b>, als auch das <b>homologe endogeneous Gene
196
+ gesilenced</b> werden.'
197
+ br
198
+ e 'Der Effekt wird durch <b>dsRNA</b> hervorgerufen.'
199
+ br
200
+ e 'Es wurde zuerst in Pflanzen, dann in Pilzen und auch in Tieren
201
+ beobachtet - vor allem die Cosuppression in Petunias wurde bekannt:'
202
+ br
203
+ dimg 'science/biology/PLANTS/COSUPPRESSION_IN_PETUNIAS.gif',
204
+ 'bblack3 marl2em'
205
+ br
206
+ e 'Picture above: A variegated petunia. Upon injection of the
207
+ gene responsible for purple colouring in petunias, the flowers
208
+ became variegated or white rather than deeper purple as was
209
+ expected.','italic marl2em smaller'
210
+ br
211
+ e 'Cosuppression führt effektiv zur <b>Degradierung von RNA</b>.'
212
+ br
213
+ e 'Dies kann man dann auch "grafting-induced" Cosuppression nennen,
214
+ vor allem in Pflanzen.'
215
+ br
216
+ ee 'Man vermutet das dieser Mechanismus in eukaryotischen Organismen
217
+ dadurch entstand um molekulare Parasiten wie Viren oder Transpososon
218
+ zu "bekämpfen" (Kasschau, K.D. & Carrington, J.C. Cell 95, 461-470 (1998). '
219
+ abr_self 'https://www.ncbi.nlm.nih.gov/pubmed/9827799?dopt=Abstract&holding=npg)'
220
+ br
221
+ e 'Diese Vermutung wird unterstützt von der Tatsache das einige
222
+ Pflanzen RNA-Viren <b>Cosuppression inhibieren</b> können.'
223
+ br
224
+ abr 'https://www.nature.com/ng/journal/v21/n2/full/ng0299_148.html',
225
+ content: 'Cosuppression'
226
+ }
227
+ # ========================================================================= #
228
+ # === IMG TAG
229
+ # ========================================================================= #
230
+ div(id: 'codon') {
231
+ dimg 'science/biology/RNA_BASE_CODE.png',
232
+ 'bblack3'
233
+ }
234
+ # ========================================================================= #
235
+ # === Methylcytosin und Methyl.
236
+ # ========================================================================= #
237
+ div('mart1em','methylcytosin') {
238
+ p {
239
+ e 'In eukaryotischer DNA liegen methylierte Cytosine immer neben
240
+ Guaninen desselben Stranges. (<b>CpG</b> Inseln, wobei p für
241
+ <b>Phosphodiesterbrücke</b> steht)'
242
+ br
243
+ e 'Häufig kann man in Bakterien methylierte Adenin-Rest finden -
244
+ <b>6-Methylaminopurin</b>.'
245
+ }
246
+ }
247
+ # ========================================================================= #
248
+ # === Meiose tag
249
+ # ========================================================================= #
250
+ header 'Meiose (griechisch: <b>meiono</b> = vermindern)'
251
+ div {
252
+ p {
253
+ e 'Die <b>Prophase I</b> der Meiose ist unterteilt in: (LeZyPaDip-Dia)'
254
+ br
255
+ cmd ' Leptotän'
256
+ cmd ' Zygotän'
257
+ cmd ' Pachytän'
258
+ cmd ' Diplotän'
259
+ cmd ' Diakinese'
260
+ }
261
+ }
262
+ # ========================================================================= #
263
+ # === F-Plasmid PHAGE
264
+ # ========================================================================= #
265
+ div(id: 'f_plasmid'){
266
+ h4 'F Plasmid'
267
+ p {
268
+ e 'Das F Plasmid insertiert mittels IS Sequenzen.'
269
+ }
270
+ }
271
+ # ========================================================================= #
272
+ # === CCA adding Enzyme
273
+ # ========================================================================= #
274
+ header 'CCA adding Enzyme'
275
+ div {
276
+ p('default') {
277
+ lem 'An dieser Stelle werden einige Fakten zum <b>CCA-adding Enzyme</b>
278
+ erwähnt.'
279
+ br
280
+ lem "Dieses Enzym hängt an 3' Ende von tRNAs die Sequenz <b>CCA</b> an."
281
+ br
282
+ lem 'Interessanterweise will dieses Enzym lieber CCC hinzufügen,
283
+ die Anwesenheit von ATP verhindert dies jedoch, und so wird
284
+ als letzter Schritt ein Adenin hinzugefügt.'
285
+ br
286
+ lem 'ATP scheint auch das weitere Hinzufügen von Cytosin zu verhindern.'
287
+ br
288
+ lem 'Mit anderen Worten - E. coli CCA enzyme ist eigentlich eine
289
+ poly(C) Polymerase, aber dank der Gegenwart von ATP
290
+ wird die Spezifität geändert.'
291
+ br
292
+ lem 'Dies erinnert an die poly(A) polymerase.'
293
+ }
294
+ }
295
+ # ========================================================================= #
296
+ # Chemische Struktur von DNA
297
+ # ========================================================================= #
298
+ header 'Chemische Struktur der DNA'
299
+ div {
300
+ dimg :chemische_struktur_dna,
301
+ 'bblack1 marl1em'
302
+ }
303
+ # ========================================================================= #
304
+ # === Wobble Regeln in der Genetik
305
+ # ========================================================================= #
306
+ div {
307
+ h2 'Wobble Regeln in der Genetik',
308
+ 'marb2px',
309
+ 'wobble' # rf stdk wobble
310
+ table2('marl2em pad0_5em','','RANDOM_BORDER_2PX',
311
+ "<b>5' end of Anticodon (tRNA)</b>","<b>3' end of Codon (mRNA)</b>",
312
+ 'G','C/U',
313
+ 'A','U',
314
+ 'C','G',
315
+ 'U','A/G',
316
+ 'I','U/C/A'
317
+ )
318
+ }
319
+ # ========================================================================= #
320
+ # === Phenylthiocarbamide tag
321
+ # ========================================================================= #
322
+ div {
323
+ h2 'PTC - Phenylthiocarbamide'
324
+ p {
325
+ dimg 'science/chemistry/PHENYLTHIOCARBAMIDE.png'
326
+ br
327
+ e '<b>Phenylthiocarbamide</b> ist eine organische Verbindung, die
328
+ entweder sehr bitter schmeckt, oder überhaupt nicht - je nachdem
329
+ welche Gene der Träger hat. (Die Fähigkeit PTC zu schmecken
330
+ ist ein dominante Eigenschaft des Gens, und der Test auf
331
+ <b>PTC Sensitivity</b> ist einer der häufigsten genetischen
332
+ Tests bei Menschen.)'
333
+ }
334
+ }
335
+ # ========================================================================= #
336
+ # === Hyperchromizität
337
+ # ========================================================================= #
338
+ h4 'Hyperchromizität'
339
+ p {
340
+ e '<b>Einzelsträngige DNA</b> absorbiert Ultraviolettstrahlung anders
341
+ als doppelsträngige DNA. Bei einer Wellenlänge von <b>260nm</b>
342
+ absorbiert ssDNA diese Strahlung 1,4 mal mehr als dsDNA - dies
343
+ ist mit dem Begriff <b>Hyperchromizität</b> gemeint.'
344
+ }
345
+ # ========================================================================= #
346
+ # === andi tag
347
+ # ========================================================================= #
348
+ div('default') {
349
+ h2 'ANDi','','andi'
350
+ dimg 'science/biology/ANIMALS/ANDi.jpg',
351
+ 'bblack3'
352
+ e 'Der Affe ANDi - reverser Name, für <i class="BOLD ud">integrated
353
+ DNA</i> wurde 2000 gezeugt.'
354
+ p {
355
+ e 'Im <b>Januar 2000</b> erblickte ANDi in einem Labor der <b>Oregon
356
+ Health Science University</b> das Licht der Welt: Als erster
357
+ transgener Rhesusaffe, der Erbinformationen einer anderen Art
358
+ in seinen Zellen trägt.'
359
+ br
360
+ e 'Das aufwändige Experiment mit hoher Fehlerquote löste
361
+ kontroverse Diskussionen aus.'
362
+ }
363
+ p {
364
+ e 'Leicht war der Weg zu diesem Erfolg nicht: <b>224 Eizellen</b> von
365
+ Rhesus-Affen wurden mit dem Quallen-Gen manipuliert. Nach der künstlichen
366
+ Befruchtung dieser Eizellen entstanden 40 Embryos. Die wurden wiederum in
367
+ 20 Leihmütter eingepflanzt, von denen nur fünf schwanger wurden. Nur
368
+ drei Affenbabys kamen am Ende lebend zur Welt - ANDi und seine
369
+ Spielkameraden. Doch nur ANDi trägt das Leuchtgen in seinem Erbgut.'
370
+ }
371
+ p {
372
+ e '<b>Wie</b> wurde <b>ANDi</b> manipuliert?'
373
+ br
374
+ e 'Die Forscher injizieren <b>nicht-infektiöse Viren</b> in eine unbefruchtete
375
+ Eizelle. Die DNA des Virus ist gleichzeitig Träger des Leuchtgens. Sie
376
+ dringt in die Chromosomen der unbefruchteten Eizelle ein. Dort baut sich
377
+ das fremde Gen in die DNA des Empfängers ein. Das Erbgut der Eizelle
378
+ trägt jetzt das Gen einer Qualle.'
379
+ }
380
+ p {
381
+ e 'Im nächsten Schritt wird das Ei künstlich befruchtet und der Embryo
382
+ einer Leihmutter eingepflanzt. Nach fünfeinhalb Monaten Schwangerschaft
383
+ wird Andi geboren. Unter dem Mikroskop wird sichtbar, dass das
384
+ Experiment geglückt ist:'
385
+ br
386
+ e 'Seine Körperzellen leuchten in fluoreszierendem Grün.','marl1em'
387
+ br
388
+ e 'Das Problem das Gerald Schatten von der Oregon Health University
389
+ hatte war das es keine isolierten Affen ES Zellen gab.'
390
+ br
391
+ e 'Als Alternative musste man einen Retrovirus verwenden, um
392
+ eine Integration der viralen DNA in die DNA der Zelle zu
393
+ ermöglichen.'
394
+ br
395
+ e 'Die Form des Retrovirus war ein "pseudo-typed retrovirus" -
396
+ es kann noch ins Genom integrieren, kann aber keine Krankheit
397
+ mehr auslösen da die meisten anderen Gene entfernt wurden.'
398
+ }
399
+ p {
400
+ e 'By placing a foreign gene (transgene) into a pseudo-typed
401
+ retrovirus and injecting the virus into the ova of an
402
+ organism, the foreign gene is integrated into the eggs&#8217;
403
+ DNA.'
404
+ br
405
+ e 'In vitro fertilization can then be used to produce embryos. Every cell in the resulting
406
+ embryo carries the foreign gene because every cell comes from
407
+ the original fertilized ovum.'
408
+ br
409
+ e 'This is the strategy used by the scientists to insert the GFP gene
410
+ into a rhesus monkey.'
411
+ br
412
+ e 'The problem with this strategy is that there is no control over the site
413
+ of integration of the transgene.'
414
+ e 'Integration into the genome is random, and this can have unwanted side-effects.'
415
+ e 'If the transgene inserts into another gene, the functioning of that gene can
416
+ be altered or completely eliminated which may result in developmental defects.'
417
+ }
418
+ p {
419
+ e 'Ein Hauptproblem dabei ist, das die Integration ins Genom zufällig erfolgen
420
+ kann - und an manchen Stellen im Genom wird diese Information überhaupt
421
+ nicht mehr aufgerufen, und damit auch nicht mehr produziert.'
422
+ }
423
+ p {
424
+ e ' A. W. S. Chan, K. Y. Chong, C. Martinovich, C. Simerly, G. Schatten*,
425
+ "Transgenic Monkeys Produced by Retroviral Gene Transfer into Mature Oocytes"
426
+ Science, Vol. 291, pp. 309-312 (January 12, 2001).'
427
+ br
428
+ a 'https://www.sciencemag.org/cgi/content/abstract/291/5502/309',
429
+ content: 'Abstract',
430
+ css_class: 'BOLD mars1em'
431
+ }
432
+ }
433
+ # ========================================================================= #
434
+ # === pathways tag
435
+ # ========================================================================= #
436
+ h2 'Genetic and Biochemical Pathways'
437
+ div('default') {
438
+ p {
439
+ e 'Neurospora Merksatz:'
440
+ br
441
+ e 'Ornithin-Citrullin-Arginin (<b>OCA</b>)',
442
+ 'marl2em'
443
+ }
444
+ }
445
+ # ======================================================================= #
446
+ # === Das Werner Syndrom
447
+ # ======================================================================= #
448
+ header 'Werner Syndrom (WS)'
449
+ div {
450
+ e 'Werner Syndrome (WS) is a rare progeroid disorder that gives
451
+ rise to <b class="ud">rapid aging phenotype</b> and increased cancer
452
+ predisposition.'
453
+ br
454
+ e 'WS is caused by mutations to a single gene, WRN, that was
455
+ identified in 1997.'
456
+ br
457
+ e 'WRN encodes for a <b>1432 amino acid protein</b>, WRN, that is
458
+ known to contain both exonuclease and helicase activities.'
459
+ br
460
+ e 'WRN belongs to the <b>RecQ helicase</b> family of genes, the
461
+ first member of which was discovered in E. coli. The family is
462
+ quite ubiquitously spread throughout the three domains of life.'
463
+ br
464
+ e 'A RecQ helicase is present as a single copy in most unicellular
465
+ organisms and multiple copies in higher eukaryotes. Five RecQ
466
+ helicases are present in humans, three of which give rise to
467
+ genetic defects, WS, Bloom syndrome (BS) and Rothmund-Thomson
468
+ syndrome (RTS).'
469
+ br
470
+ e 'However, WRN is unique among RecQ helicases
471
+ in coupling an exonuclease domain coupled to a helicase
472
+ domain, on the same polypeptide.'
473
+ br
474
+ dimg 'science/WERNER_SYNDROME.jpg',
475
+ 'marl1em bblack1'
476
+ }
477
+ # ========================================================================= #
478
+ # === Pedigree symbols explained
479
+ # ========================================================================= #
480
+ h2 'Pedigree symbols explained'
481
+ div('default') {
482
+ dimg 'science/genetics/pedigree_symbols_explained.png',
483
+ 'bblack1 mars3em'
484
+ }
485
+ # ========================================================================= #
486
+ # === Slogans
487
+ # ========================================================================= #
488
+ h2 'Slogans'
489
+ p_default {
490
+ e '- The minor DNA groove is less rich in chemical information
491
+ than is the major DNA groove.'
492
+ br
493
+ e '- Each gene discovery project begins with a hunt for mutants
494
+ affecting the biological process that is the focus of the
495
+ research.'
496
+ br
497
+ e '- In Bakterien kodiert <b>rpoH</b> für den Sigmafaktor 32.'
498
+ br
499
+ e '- Das Trockengewicht einer typischen Prokaryotenzelle
500
+ besteht zu rund 50% aus Kohlenstoff.'
501
+ br
502
+ e '- In Textilien wird oft <b class="FI">Lindan</b> verwendet,
503
+ ein Giftstoff.'
504
+ br
505
+ e '- <b>Aldosteron</b> scheint mitzuhelfen, das man im Alter besser hört.'
506
+ br
507
+ e '- DNA is the ultimate molecule.'
508
+ br
509
+ e '- Epigenetic silencing can be inherited from one cell
510
+ generation to the next.'
511
+ br
512
+ e '- Can an organism be conceived of as a mere mosaic of
513
+ traits determined by genes?'
514
+ br
515
+ e '- The genome is the living blueprint of an organism.'
516
+ br
517
+ e '- At around the time when the word genes was defined,
518
+ genes could be regarded as abstract elements in an
519
+ equally abstract space.'
520
+ br
521
+ e '- Conjugation is sex-like fusion.'
522
+ br
523
+ e '- RNA ist reaktiver als DNA, da der Zucker eine zusätzliche
524
+ OH-Gruppe am 2-prime C-Atom enthält.'
525
+ br
526
+ e '- One common grouping of transposable elements is whether
527
+ they have to make use of reverse transcription in order to
528
+ transpose or whether they do not.'
529
+ br
530
+ e 'Die verfügbare Anzahl an tRNAs in einer Zelle mag sich
531
+ auf die Geschwindigkeit der Translation auswirken. Wenn bestimmte
532
+ tRNAs nur selten vorkommen, dann wird das Ribosom bei
533
+ der Translation nicht zügig voranschreiten können.'
534
+ br
535
+ e '- As early as the 1920s, many geneticists ­came to believe
536
+ that genes must be mate­rial particles.'
537
+ br
538
+ e '- Autocatalysis in genetics refers to the capacity of genes
539
+ to initiate synthetic processes that ultimately yield copies
540
+ of the genes themselves in order to propagate the genetic
541
+ material from cell to cell and from generation to generation.'
542
+ br
543
+ e '- The F-plasmid can assume both an autonomous and an
544
+ integrated state.'
545
+ br
546
+ e '- CpG (CG) in eukaryotic DNA acts as an <b>epigenetic
547
+ signal</b>.'
548
+ br
549
+ e '- Genetically identical twings might still be epigenetically different.'
550
+ br
551
+ e '- Centromeres are epigenetically defined.'
552
+ br
553
+ e '- Chromatin structure is able to regulate the expression of genes.'
554
+ br
555
+ e '- Classical genetics was a method to expand biological knowledge.'
556
+ br
557
+ e '- Geneticists make a large proportion of their inferences by
558
+ manipulating the system and observing the effects.'
559
+ br
560
+ e '- Maternal imprinting means that a copy of a gene derived from
561
+ the mother will become inactivated.'
562
+ br
563
+ e '- The highly efficient system of homologous recombination in
564
+ Yeast allows the alteration of any chosen chromosomal
565
+ sequence at will.'
566
+ br
567
+ e '- AUGA ist eine besondere Sequenz, da sie sowohl ein Startcodon
568
+ (AUG) als auch ein Stopcodon (UGA) besitzt.'
569
+ br
570
+ e '- The hunt for the molecular basis of heredity began in earnest
571
+ with an experiment by Frederick Griffith, who was wirking with
572
+ a virulent strain of Streptococcus pneumoniae.'
573
+ br
574
+ e '- The Avery–MacLeod–McCarty experiment in 1944 showed that
575
+ the "transforming principle" is in fact DNA.'
576
+ br
577
+ e '- Crossovers können sich gegenseitig inhibieren, das heisst
578
+ das in unmittelbarer Nähe eines Crossovers kein weiteres
579
+ auftritt.'
580
+ br
581
+ e '- All cells are unified by the facts that their genetic
582
+ blueprints are encoded in DNA.'
583
+ br
584
+ e "- Alfred Sturtevant's experiments showed that the phenotypic
585
+ expression of a mutation could be affected by the loca­tion of
586
+ the mutated gene on the chromosome."
587
+ br
588
+ e '- Chromatin loops are a higher level of chromatin structure.'
589
+ br
590
+ e '- RNA folds up by intramolecular base pairing.'
591
+ br
592
+ e '- Die Aufgabe von mTORC1 ist es die Translation von
593
+ Proteinen zu aktivieren.'
594
+ br
595
+ e '- Imprinted genes can often be found to be clustered together,
596
+ aka aggregated as a unit.'
597
+ br
598
+ e '- Plasmids are often important for virulence; for
599
+ instance, <i>Bacillus</i> anthracis has 2 plasmids required
600
+ for is virulence properties.'
601
+ br
602
+ e '- Die Modifikation von Histonen verändert die
603
+ Chromatinfunktion.'
604
+ br
605
+ e '- The diploid character of the eukaryotic cell allows for
606
+ a mutation in one gene to be masked by a second, unmutated
607
+ gene copy.'
608
+ br
609
+ e '- Die Telomerase regeneriert die Telomere.'
610
+ br
611
+ e '- Die SRY-Region kann sich "bewegen", zum Beispiel auf
612
+ das X-Chromosom.'
613
+ br
614
+ e '- Heterochromatin propagates from a nucleation event.'
615
+ br
616
+ e '- Perizentrische Inversionen kann man oft daran
617
+ erkennen, das das Centromer seine Position im
618
+ Chromosom ändert.'
619
+ br
620
+ e '- Die Funktion des Zellkerns ist die Aufbewahrung
621
+ der DNA.'
622
+ br
623
+ e '- HP-1, heterochromatin protein-1, is required in
624
+ some way to generate the higher order chromatin
625
+ structure associated with heterochromatin.'
626
+ br
627
+ e '- DNA Methylation acts as an epigenetic mark.'
628
+ br
629
+ e '- Der Unterschied zwischen dem Menschen- und Schimpansengenom
630
+ liegt hauptsächlich in der chromosomalen Organisation (und
631
+ nicht in der DNA Sequenz)'
632
+ br
633
+ e '- Der Spindel-Checkpoint arretiert die Teilung bis alle
634
+ Chromosomen richtig in der Spindel angeordnet sind.'
635
+ br
636
+ e '- Transposons create mutations and can thusly be considered to
637
+ be one of the raw materials for evolution.'
638
+ br
639
+ e '- The dark-staining bands in polytene chromosomes act as
640
+ useful chromosomal landmarks.'
641
+ br
642
+ e '- In most diploid eukaryotes, sexual reproduction is the
643
+ only natural mechanism for producing new members of the
644
+ species.'
645
+ br
646
+ e '- The total gene content of all organisms inhabiting an
647
+ environment is known as its metagenome.'
648
+ br
649
+ e '- In Eukaryoten ist die Termination der Transkription
650
+ eng gekoppelt mit dem <b>Poly-Adenylierungssignal</b>.'
651
+ br
652
+ e '- Hfq acts as a RNA chaperone.'
653
+ br
654
+ e '- Die Behinderung der Segregation nur eines Chromosoms
655
+ vereitelt die Segregation auch aller anderen Chromosomen.'
656
+ br
657
+ e '- Overlapping genes are coupled, meaning that if you
658
+ manipulate one gene, the other coupled gene might be
659
+ affected by this change as well. Thus, this constitutes
660
+ a design constraint.'
661
+ br
662
+ e '- Eine Gensequenz ohne Promotor bleibt stumm.'
663
+ br
664
+ e '- RNA-Moleküle haben nur eine begrenzte Lebensdauer
665
+ ("half-life") in der Zelle.'
666
+ br
667
+ e '- Exon to Intron comparison revealed that exons happen
668
+ to have a low "signal-to-noise" ratio in the human genome.'
669
+ br
670
+ e '- Exons can be skipped in alternative splicing.'
671
+ br
672
+ e '- Die Verteilung des Spo11 Proteins entlang der Chromosomen
673
+ korreliert mit dem Auftreten meiotischer Doppelstrangbrüche.'
674
+ br
675
+ e '- H2AX becomes phosphorylated at sites of DNA-strand
676
+ breakage.'
677
+ br
678
+ e "- Whereas prokaryotic genes are generally accessible and
679
+ 'on' unless repressed, eukaryotic genes are inaccessible
680
+ and 'off' unless activated."
681
+ br
682
+ e '- Transcription is repressed when the promoter is wound
683
+ up in a nucleosome.'
684
+ br
685
+ e '- Ein "scaffold complex" beschleunigt die Reinitiation
686
+ der DNA-Replikation, die dadurch schneller ablaufen kann.'
687
+ br
688
+ e '- In mammals, X chromosome inactivation begins at the
689
+ XIC (X-Inactivation Center).'
690
+ br
691
+ e '- siRNA ultimately helps protect the integrity of
692
+ genomes.'
693
+ br
694
+ e '- A phosphorylation / dephosphorylation cycle controls
695
+ transription and RNA maturation.'
696
+ br
697
+ e '- Die 30nm DNA-Fiber entsteht in dem der Histon-DNA
698
+ Komplex sich zu zu dieser Faser windet.'
699
+ br
700
+ e '- Chiasmen sind die cytologisch sichtbare Folge
701
+ von Crossovers in Diplotän und Diakinese.'
702
+ br
703
+ e '- Eine Chromodomäne kann methylierte Histone erkennen.'
704
+ br
705
+ e '- "Crossing over" durchbricht die chromosomale Kopplung
706
+ von Genen.'
707
+ br
708
+ e '- Jede aktive Polymerase führt zur Entstehung einer
709
+ "<i>transcription bubble</i>".'
710
+ br
711
+ e '- XIC constitutes a genomic locus for non-coding RNAs
712
+ that orchestrate the inactivation of extra X chromosomes
713
+ in mammalian cells.'
714
+ br
715
+ e '- Verschiedene Abschnitte im Chromosom werden zu
716
+ unterschiedlichen Zeiten in der S-Phase repliziert.'
717
+ br
718
+ e '- To maintain the stability of a species, replication
719
+ of the DNA of a given organism must be almost free of
720
+ error.'
721
+ br
722
+ e '- Jedes Bivalent hat mindestens immer ein
723
+ Crossover-Ereignis, so klein dies auch immer sein
724
+ mag. Dies ist unbedingt nötig, da ansonsten homologe
725
+ Chromosomen nicht voneinander segregieren können.'
726
+ br
727
+ e '- Bei Kälte mögen Sekundärstrukturen in der RNA zu stabil
728
+ werden.'
729
+ br
730
+ e '- Pol III Promoters are located downstream from
731
+ the transcription start site.'
732
+ br
733
+ e '- Alternatives Splicing führt zur Diversifizierung des
734
+ Proteoms.'
735
+ br
736
+ e '- In eukaryotes, transcription levels are made finely
737
+ adjustable in a chromatin environment by clustering
738
+ binding sites into enhancers.'
739
+ br
740
+ e '- Epigenetic Mechanisms lead to heritable changes in
741
+ gene functions which are not based on changes in the
742
+ DNA Sequence itself.'
743
+ br
744
+ e '- <b>IRES</b> are RNA sequences that function like
745
+ <b>prokaryotic RBS</b>.'
746
+ br
747
+ e '- In contrast with the customary picture of DNA as
748
+ an extended double helix, structural deformation of
749
+ DNA to bend or fold into a more compact form is the
750
+ rule rather than an exception.'
751
+ br
752
+ e '- Wenn sich neu synthetisierte DNA-Moleküle (die
753
+ Chromatiden) nicht auf Tochterkerne aufteilen können
754
+ entstehen polyploide Zellkerne.'
755
+ br
756
+ e '- Eine wahrscheinliche Ursache für die Entstehung
757
+ von Aneuploidien ist die verminderte Cohäsion der
758
+ Schwesterchromatiden.'
759
+ br
760
+ e '- Innerhalb der Chromosomendomänen ("chromosomal
761
+ territories") im Zellkern ist das Chromatin
762
+ <b>nicht</b> zufällig angeordnet.'
763
+ br
764
+ e '- Ein Sigmafaktor steuert die Fähigkeit der RNA
765
+ Polymerase Promoter-DNA von anderer DNA zu
766
+ unterscheiden; man spricht hierbei von
767
+ "Diskriminierung von DNA Elementen".'
768
+ br
769
+ e '- The SWI-SNF complex can <b>reposition nucleosomes</b>
770
+ in a test-tube assay if ATP is provided as an
771
+ energy source.'
772
+ br
773
+ e '- Elongation, Termination of Transcription and RNA
774
+ processing are interconnected to one another.'
775
+ br
776
+ e '- Incorporation of Histone H3.3 serves as an
777
+ epigenetic mark for <b>transcriptionally active
778
+ chromatin</b>.'
779
+ br
780
+ e '- Ligand binding of RNA often produces a change in
781
+ the secondary structure of RNA.'
782
+ br
783
+ e '- DNA functions as <b>a template for biological
784
+ complexity</b>.'
785
+ br
786
+ e '- The ribosome behaves like a small, migrating
787
+ factory.'
788
+ br
789
+ e '- mRNA nonsense mutation may trigger degradation of mRNA.'
790
+ br
791
+ e '- mRNA dient als Template für protein synthesis und
792
+ wird als Ribonucleprotein exportiert.'
793
+ br
794
+ e '- Signaling Pathways are the superhighways of the cell.'
795
+ br
796
+ e '- All tRNAs must conform to the same structure (in 3D).'
797
+ br
798
+ e '- Nucleosomes are inhibitors of transcription because
799
+ DNA is packed very tightly and is not accessible for
800
+ RNA polymerases while condensed.'
801
+ br
802
+ e '- DNA Melting im Zuge der Transkription geschieht am
803
+ -10 Bereich; somit ist die -10 Region wichtiger als die
804
+ -35 Region in Bezug auf die Genexpression.'
805
+ br
806
+ e '- tRNA-Synthetases provide a docking platform for
807
+ aminoacids and their cognate tRNAs.'
808
+ br
809
+ e '- TFIIH controls the ATP-dependent transition of the
810
+ preinitiation complex to the open complex.'
811
+ br
812
+ e '- Sobald mehr als 10 Nukleotide synthetisiert worden
813
+ sind, escaped die Polymerase vom Promoter.'
814
+ br
815
+ e '- Nucleosomes are an invariant component of euchromatic
816
+ and heterochromatin in the interphase nucles and of
817
+ mitotic chromosomes.'
818
+ br
819
+ e '- Heterochromatin can serve as a defense mechanism
820
+ against foreign DNA, by silencing transposons.'
821
+ br
822
+ e '- Point mutations in the promoter and promoter-proximal
823
+ elements hinder transcription of the Beta-globin gene.'
824
+ br
825
+ e '- LCRs und Insulator-Sequenzen können transkribierte
826
+ und nicht-transkribierte Bereiche durch die Bildung von
827
+ "chromatin-hubs" voneinander trennen.'
828
+ br
829
+ e '- Histone N-terminal tails provide a molecular handle
830
+ to manipulate DNA accessibility in chromatin.'
831
+ br
832
+ e '- CTD Phosphorylierung bestimmt bestimmen wann
833
+ Proteine an den Polymerasekomplex binden können im
834
+ Zuge der Transkription.'
835
+ br
836
+ e '- Barrier insulators prevent the spreading of
837
+ heterochromatin by creating a local environment
838
+ unfavourable to heterochromatin formation.'
839
+ br
840
+ e '- Inactivation spreads from heterochromatin
841
+ into the adjacent region for a variable distance.'
842
+ br
843
+ e '- Bei <b>Translokations-Trisomien</b> ist der Grund für
844
+ die Entstehung eines aneuploiden Gameten eine Fusion
845
+ von Chromosomen, gefolgt von einem meiotischen
846
+ Paarungs- und Segregations-Defekt des in der Regel
847
+ kleineren Fusionspartners.'
848
+ br
849
+ e '- A barrier insulator can recruit HATs (Histone
850
+ Acetyltransferases) and, in doing so, ensure that
851
+ the adjacent histones are hyperacetylated.'
852
+ br
853
+ e '- Historically DNA seemed to be far too simple and
854
+ too unspecific to support complex biological functions.'
855
+ br
856
+ e '- The stereochemical fit between A=T and C☰G in
857
+ dsDNA is mediated by hydrogen bonds.'
858
+ br
859
+ e '- Sister chromatids are held together by the multi-subunit
860
+ protein complex called <b>cohesin</b>.'
861
+ br
862
+ e 'Shugoshin protects cohesin from being degraded by
863
+ separase at the centromeric regions.'
864
+ br
865
+ e '- Genetic information is ultimately equivalent to
866
+ biochemical function.'
867
+ br
868
+ e '- Molecular genes are not solely confined to being separate "units"
869
+ of inheritance. More importantly they act as a complex assemblages
870
+ of diverse activating and inhibiting mechanisms, acting in concert
871
+ to transcribe and translate DNA templates of various makeup into
872
+ functional protein products.'
873
+ br
874
+ e '- Genetics proceeds from the realm of DNA and its
875
+ replication, to the realm of its transcription, and
876
+ finally to that of its translation.'
877
+ br
878
+ e '- The molecular gene is not defined by its physical and
879
+ chemical materiality on the level of DNA, but rather by
880
+ the products that result from its activity.'
881
+ br
882
+ e '- The capacity for autocatalysis is inherent not only in
883
+ "ordinary" genes but in other DNA elements as well, thus
884
+ questioning the original (historic) definition of the gene
885
+ concept.'
886
+ br
887
+ e '- In 1956, Arthur Kornberg isolated the first DNA polymerase.'
888
+ br
889
+ e '- Gene technology allowed genetic engineers to modify model
890
+ organism with new characteristics. Bacteria could serve as
891
+ some kind of bioreactor.'
892
+ br
893
+ e '- By virtue of being patented, genes additionally assumed
894
+ the character of commodities.'
895
+ br
896
+ e '- The Human Genome Project (HGP) stressed the
897
+ detrimental, but curable role of genes in disease
898
+ for its promotion.'
899
+ br
900
+ e '- Efforts to automate DNA sequencing began in the
901
+ early 1980s.'
902
+ br
903
+ e '- The promise of medical salvation was very effective
904
+ in convincing politicians to support the Human Genome
905
+ Project.'
906
+ br
907
+ e '- An example for genetic polmorphism is the fact that
908
+ the genomes of different human individuals exhibit
909
+ considerable differences.'
910
+ br
911
+ e '- Some epigenetic factors can be named as an example
912
+ that allows for information to pass from the environment
913
+ to the genome, at the least in some organisms.'
914
+ br
915
+ e '- The pax6 gene product is multifunctional as well as
916
+ redundant, to some extent. The Drosophila genome, for
917
+ instance, contains several isoforms with virtually identical
918
+ effects on eye formation.'
919
+ br
920
+ e '- Not every feature of a genome may carry some function
921
+ that is essential to the survival of the organism.'
922
+ br
923
+ e '- The sequences that are annotated as "genes" represent
924
+ only one set of the components of complex genomic ensembles.
925
+ Thus, what is a gene is not necessarily an intrinsic property
926
+ of the DNA sequence at hand, but subject to interpretation
927
+ and evaluation by the genetic "decipher" system in use, by
928
+ the corresponding cell at hand.'
929
+ br
930
+ e '- In regards to genetic mutations that affect an individual
931
+ human being negatively, we can state that each embryo is
932
+ (indirectly) playing "a game of genomic Russian roulette".'
933
+ br
934
+ e '- Many of these diseases that will afflict children are
935
+ knowable in advance, before a couple even conceives.'
936
+ br
937
+ e '- Most genomic changes outside of protein-coding regions are
938
+ not incompatible with vital (living) functions of a complex
939
+ organism - such as a human being - at hand.'
940
+ br
941
+ e '- Genetics is a form of information science.'
942
+ br
943
+ e '- The old blending theory of inheritance in genetics can be
944
+ roughly summarized as "the belief that inheritance worked like
945
+ the mixing of fluids, such as paints".'
946
+ br
947
+ e '- Genetic defects can create chemical individuality among
948
+ humans.'
949
+ br
950
+ e '- The shorter the generation time, the sooner the experiments
951
+ can be completed.'
952
+ br
953
+ e '- An ethical dilemma in regards to engineering human beings
954
+ in the future may be that any genetically engineered,
955
+ homogeneous children will be scrubbed of genomic individuality.'
956
+ br
957
+ e '- It would be a great feat of engineering to reduce the
958
+ burden of genetic disease while preserving the genomic
959
+ diversity of the human species.'
960
+ br
961
+ e '- Genetic variation is any difference between two copies of
962
+ the same gene or DNA molecule.'
963
+ br
964
+ e '- In vitro fertilization (IVF) could be used to eliminate
965
+ (some) genetic disease, such as via <b>pre-implantation
966
+ genetic testing</b> (PGT).'
967
+ br
968
+ e '- Genomic design in humans, aside from ethical considerations
969
+ in regards to similar problems faced by eugenics, may considerably
970
+ reduce the burden of recessive genetic diseases and some forms
971
+ of dominant genetic disease.'
972
+ br
973
+ e '- Fathers contribute four times as many new mutations to their
974
+ offspring as do mothers.'
975
+ br
976
+ e '- Intronic sequences found in DNA are spliced out to produce a
977
+ mature mRNA.'
978
+ br
979
+ e '- Mitochondrial disorders can result from alterations in nuclear
980
+ or mitochondrial genes.'
981
+ br
982
+ e '- Mutants allow a geneticist to <i>zero in on any genetic
983
+ property</i>.'
984
+ br
985
+ e '- Translocation events can disrupt critical and essential genes.'
986
+ br
987
+ e "- Biological organisms can be viewed as nature's versatile
988
+ engines of creation."
989
+ br
990
+ e '- In haploids, all alleles are expressed in the phenotype
991
+ because there is no masking of recessives by dominant alleles
992
+ on the other homolog.'
993
+ br
994
+ e '- In a diploid organism, a sterile recessive mutant can be
995
+ propagated as a heterozygote.'
996
+ br
997
+ e '- Genetics is to turn the inorganic into the organic.'
998
+ br
999
+ e '- Alternatives Spleißen vermehrt die Codierungsmöglichkeiten
1000
+ eines Gens.'
1001
+ br
1002
+ e '- Genetics, respectively genomics, is <b>the tale of the
1003
+ genome</b>.'
1004
+ br
1005
+ e '- The story of DNA and RNA replication is that of
1006
+ <b>complementary surfaces</b>.'
1007
+ br
1008
+ e '- Diagnostic breast cancer genetic diagnostics, such as for
1009
+ the BRCA1 and BRCA2 gene, is owned by <b>Myriad Genetics</b>.'
1010
+ br
1011
+ e '- With the expression <b>a gene for a disease</b> we typically
1012
+ refer to a <b>mutation</b> in a gene that would plays a role in
1013
+ a specific disease.'
1014
+ br
1015
+ e '- Some geneticists may say that <b>the genes may load the
1016
+ gun but the environment pulls the trigger</b>.'
1017
+ br
1018
+ e '- Different RNA molecules replicate at differing rates, at the
1019
+ least in a test tube. The logical implication of this is that
1020
+ descendants of the swifter replicators naturally grow more
1021
+ common in a population.'
1022
+ br
1023
+ e '- Genes resemble manuscripts written in a four-letter alphabet.'
1024
+ br
1025
+ e '- Genes built ever more elaborate survival machines to aid
1026
+ their own replication.'
1027
+ br
1028
+ e '- RNA replicating in test tubes shows how the idea of purpose
1029
+ can apply to "mindless molecules".'
1030
+ br
1031
+ e '- Genetik ist die universelle biologische Disziplin.'
1032
+ br
1033
+ e '- DNA is at the center of the mystery of heredity.'
1034
+ br
1035
+ e '- Genetic evolution prefers to refine and extend existing
1036
+ information rather than create genuinely new information.'
1037
+ br
1038
+ e '- Genetic engineering yields the power to shape life.'
1039
+ br
1040
+ e '- Erbliche Eigenschaften legen einen Bereich fest, in dem
1041
+ <b>Variabilität</b> möglich ist.'
1042
+ br
1043
+ e '- Synthesized mRNA is interesting because it represents
1044
+ all active genes of a given cell or tissue. It also forms
1045
+ the basis for the creation of <b>cDNA libraries</b>.'
1046
+ br
1047
+ e '- The <b>telomerase</b> is <b>an unusual type of reverse
1048
+ transcriptase</b>.'
1049
+ br
1050
+ e '- Sequences in regions adjacent to the gene itself
1051
+ are called <b>cis-acting elements</b>.'
1052
+ br
1053
+ e '- Die komplexere Organisation eines Organismus schlägt sich
1054
+ jedoch in einer höheren Anzahl von Proteinen nieder.'
1055
+ br
1056
+ e '- '+squotes('It has not escaped our notice that the specific
1057
+ pairing we have postulated immediately suggests a possible
1058
+ copying mechanism for the genetic material.')
1059
+ br
1060
+ e '- <b>DNA</b> is <b>the master recipe for life</b>.'
1061
+ br
1062
+ e '- The offspring of sexually reproducing multi-cellular
1063
+ organism receive a brand-new book that melds together
1064
+ recipes from both individual parents.'
1065
+ br
1066
+ e '- Antagnoistic pleiotropy refers to the concept of
1067
+ genes that do beneficial things early and harmful things
1068
+ later.'
1069
+ br
1070
+ e '- Extended survival means that the diseases in
1071
+ the genetic dustbin have the opportunity
1072
+ to be seen or expressed in a greater number of
1073
+ people.'
1074
+ br
1075
+ e '- Every human alive today is the most recent link in an
1076
+ unbroken chain of survivors that extends back not only to
1077
+ the originas of modern humans but to the origins of life
1078
+ on earth.'
1079
+ br
1080
+ e '- Genes play a central role in maintaining the biological
1081
+ integrity of the organism that carries them.'
1082
+ br
1083
+ e '- Natural selection is an imperfect genetic sieve that
1084
+ inevitably allows some harmful genes to leak through to
1085
+ the next generation by hitching a ride with the many genes
1086
+ that have either a neutral or beneficial effect on the
1087
+ survival and reproductive success of the individual.'
1088
+ br
1089
+ } # End of slogans tag
1090
+ # ========================================================================= #
1091
+ # === Links
1092
+ # ========================================================================= #
1093
+ h2 'Links (remote)',
1094
+ 'mart1px'
1095
+ dot104 = dot104?
1096
+ p('mars1em') {
1097
+ abr 'https://www.onmeda.de/krankheiten/krankheiten_az.html',
1098
+ content: dot104+'Verschiedene Krankheiten (auf onmeda.de)',
1099
+ css_class: 'slateblue'
1100
+ abr 'https://www.embl.org/sites/heidelberg/',
1101
+ content: dot104+'EMBL in Heidelberg',
1102
+ css_class: 'slateblue'
1103
+ }
1104
+ # ========================================================================= #
1105
+ # === Local Links tag
1106
+ # ========================================================================= #
1107
+ h2 sg(:square_yellow, 'bblack1 marr4px')+
1108
+ 'Local Links',
1109
+ 'martb2px'
1110
+ div('default martb1px') {
1111
+ p('ind0px marl2em mart1px padt1px') {
1112
+ abr_self :local_science
1113
+ }
1114
+ }
1115
+ }}