/test-data/rgtestouts/rgQC/rgQCtest1.html

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  12. <h4>
  13. <div>Output from Rgenetics QC report tool run at 19/05/2010 15:15:46<br>
  14. </h4>
  15. </div><div><h4>(Click any preview image to download a full sized PDF version)</h4><br><ol>
  16. <table cellpadding="5" border="0">
  17. <tr><td colspan="3"><a href="MarkerDetails_rgQCtest1.xls" type="application/vnd.ms-excel">Click here to download the Marker QC Detail report file</a> (1.4 KB) tab delimited</td></tr>
  18. <tr><td colspan="3"><a href="SubjectDetails_rgQCtest1.xls" type="application/vnd.ms-excel">Click here to download the Subject QC Detail report file</a> (1.4 KB) tab delimited</td></tr>
  19. <tr><td><a href="tinywga_All_Paged.pdf"><img src="tinywga_All_Paged-0.jpg" alt="All tinywga QC Plots joined into a single pdf" hspace="10" align="middle">
  20. </a></td><td>All tinywga QC Plots joined into a single pdf</td><td>&nbsp;</td></tr>
  21. <tr><td><a href="tinywga_All_3x3.pdf"><img src="tinywga_All_3x3-0.jpg" alt="All tinywga QC Plots 3 by 3 to a page" hspace="10" align="middle">
  22. </a></td><td>All tinywga QC Plots 3 by 3 to a page</td><td>&nbsp;</td></tr>
  23. <tr><td><a href="tinywga_logphweunaff.pdf"><img src="tinywga_logphweunaff.jpg" alt="Marker HWE" hspace="10" align="middle">
  24. </a></td><td>Marker HWE</td><td><a href="Ranked_Marker_HWE.xls">Worst data</a></td></tr>
  25. <tr><td><a href="tinywga_logphweunaff_cum.pdf"><img src="tinywga_logphweunaff_cum.jpg" alt="Ranked Marker HWE" hspace="10" align="middle">
  26. </a></td><td>Ranked Marker HWE</td><td>&nbsp;</td></tr>
  27. <tr><td><a href="QQtinywga_logphweunaff_cum.pdf"><img src="QQtinywga_logphweunaff_cum.jpg" alt="LogQQ plot Marker HWE" hspace="10" align="middle">
  28. </a></td><td>LogQQ plot Marker HWE</td><td>&nbsp;</td></tr>
  29. <tr><td><a href="tinywga_missfrac.pdf"><img src="tinywga_missfrac.jpg" alt="Marker Missing Genotype" hspace="10" align="middle">
  30. </a></td><td>Marker Missing Genotype</td><td><a href="Ranked_Marker_Missing_Genotype.xls">Worst data</a></td></tr>
  31. <tr><td><a href="tinywga_missfrac_cum.pdf"><img src="tinywga_missfrac_cum.jpg" alt="Ranked Marker Missing Genotype" hspace="10" align="middle">
  32. </a></td><td>Ranked Marker Missing Genotype</td><td>&nbsp;</td></tr>
  33. <tr><td><a href="tinywga_maf.pdf"><img src="tinywga_maf.jpg" alt="Marker MAF" hspace="10" align="middle">
  34. </a></td><td>Marker MAF</td><td><a href="Ranked_Marker_MAF.xls">Worst data</a></td></tr>
  35. <tr><td><a href="tinywga_maf_cum.pdf"><img src="tinywga_maf_cum.jpg" alt="Ranked Marker MAF" hspace="10" align="middle">
  36. </a></td><td>Ranked Marker MAF</td><td>&nbsp;</td></tr>
  37. <tr><td><a href="tinywga_fracmiss.pdf"><img src="tinywga_fracmiss.jpg" alt="Subject Missing Genotype" hspace="10" align="middle">
  38. </a></td><td>Subject Missing Genotype</td><td><a href="Ranked_Subject_Missing_Genotype.xls">Worst data</a></td></tr>
  39. <tr><td><a href="tinywga_fracmiss_cum.pdf"><img src="tinywga_fracmiss_cum.jpg" alt="Ranked Subject Missing Genotype" hspace="10" align="middle">
  40. </a></td><td>Ranked Subject Missing Genotype</td><td>&nbsp;</td></tr>
  41. <tr><td><a href="tinywga_s_het.pdf"><img src="tinywga_s_het.jpg" alt="Subject F Statistic" hspace="10" align="middle">
  42. </a></td><td>Subject F Statistic</td><td>&nbsp;</td></tr>
  43. <tr><td><a href="tinywga_s_het_cum.pdf"><img src="tinywga_s_het_cum.jpg" alt="Ranked Subject F Statistic" hspace="10" align="middle">
  44. </a></td><td>Ranked Subject F Statistic</td><td>&nbsp;</td></tr>
  45. <tr><td><a href="FQNormtinywga_s_het_cum.pdf"><img src="FQNormtinywga_s_het_cum.jpg" alt="F Statistic Subject F Statistic" hspace="10" align="middle">
  46. </a></td><td>F Statistic Subject F Statistic</td><td>&nbsp;</td></tr>
  47. </table><hr><h3>All output files from the QC run are available below</h3>
  48. <table cellpadding="5" border="0">
  49. <tr><td><a href="FQNormtinywga_s_het_cum.jpg">FQNormtinywga_s_het_cum.jpg</a> (30.2 KB)</td></tr>
  50. <tr><td><a href="FQNormtinywga_s_het_cum.pdf">FQNormtinywga_s_het_cum.pdf</a> (7.1 KB)</td></tr>
  51. <tr><td><a href="MarkerDetails_rgQCtest1.xls">MarkerDetails_rgQCtest1.xls</a> (1.4 KB)</td></tr>
  52. <tr><td><a href="QQtinywga_logphweunaff_cum.jpg">QQtinywga_logphweunaff_cum.jpg</a> (33.0 KB)</td></tr>
  53. <tr><td><a href="QQtinywga_logphweunaff_cum.pdf">QQtinywga_logphweunaff_cum.pdf</a> (6.6 KB)</td></tr>
  54. <tr><td><a href="Ranked_Marker_HWE.xls">Ranked_Marker_HWE.xls</a> (763 B)</td></tr>
  55. <tr><td><a href="Ranked_Marker_MAF.xls">Ranked_Marker_MAF.xls</a> (564 B)</td></tr>
  56. <tr><td><a href="Ranked_Marker_Missing_Genotype.xls">Ranked_Marker_Missing_Genotype.xls</a> (659 B)</td></tr>
  57. <tr><td><a href="Ranked_Subject_Missing_Genotype.xls">Ranked_Subject_Missing_Genotype.xls</a> (804 B)</td></tr>
  58. <tr><td><a href="SubjectDetails_rgQCtest1.xls">SubjectDetails_rgQCtest1.xls</a> (1.4 KB)</td></tr>
  59. <tr><td><a href="ldp_tinywga.bed">ldp_tinywga.bed</a> (143 B)</td></tr>
  60. <tr><td><a href="ldp_tinywga.bim">ldp_tinywga.bim</a> (392 B)</td></tr>
  61. <tr><td><a href="ldp_tinywga.fam">ldp_tinywga.fam</a> (603 B)</td></tr>
  62. <tr><td><a href="ldp_tinywga.log">ldp_tinywga.log</a> (2.0 KB)</td></tr>
  63. <tr><td><a href="tinywga.fmendel">tinywga.fmendel</a> (378 B)</td></tr>
  64. <tr><td><a href="tinywga.frq">tinywga.frq</a> (1.2 KB)</td></tr>
  65. <tr><td><a href="tinywga.het">tinywga.het</a> (2.5 KB)</td></tr>
  66. <tr><td><a href="tinywga.hwe">tinywga.hwe</a> (6.5 KB)</td></tr>
  67. <tr><td><a href="tinywga.imendel">tinywga.imendel</a> (612 B)</td></tr>
  68. <tr><td><a href="tinywga.imiss">tinywga.imiss</a> (1.9 KB)</td></tr>
  69. <tr><td><a href="tinywga.lmendel">tinywga.lmendel</a> (571 B)</td></tr>
  70. <tr><td><a href="tinywga.lmiss">tinywga.lmiss</a> (1.1 KB)</td></tr>
  71. <tr><td><a href="tinywga.log">tinywga.log</a> (1.9 KB)</td></tr>
  72. <tr><td><a href="tinywga.mendel">tinywga.mendel</a> (56 B)</td></tr>
  73. <tr><td><a href="tinywga.prune.in">tinywga.prune.in</a> (140 B)</td></tr>
  74. <tr><td><a href="tinywga.prune.out">tinywga.prune.out</a> (110 B)</td></tr>
  75. <tr><td><a href="tinywga.sexcheck">tinywga.sexcheck</a> (2.5 KB)</td></tr>
  76. <tr><td><a href="tinywga_All_3x3-0.jpg">tinywga_All_3x3-0.jpg</a> (45.2 KB)</td></tr>
  77. <tr><td><a href="tinywga_All_3x3-1.jpg">tinywga_All_3x3-1.jpg</a> (19.3 KB)</td></tr>
  78. <tr><td><a href="tinywga_All_3x3.pdf">tinywga_All_3x3.pdf</a> (82.4 KB)</td></tr>
  79. <tr><td><a href="tinywga_All_Paged-0.jpg">tinywga_All_Paged-0.jpg</a> (13.6 KB)</td></tr>
  80. <tr><td><a href="tinywga_All_Paged-1.jpg">tinywga_All_Paged-1.jpg</a> (26.3 KB)</td></tr>
  81. <tr><td><a href="tinywga_All_Paged-10.jpg">tinywga_All_Paged-10.jpg</a> (31.4 KB)</td></tr>
  82. <tr><td><a href="tinywga_All_Paged-11.jpg">tinywga_All_Paged-11.jpg</a> (29.8 KB)</td></tr>
  83. <tr><td><a href="tinywga_All_Paged-2.jpg">tinywga_All_Paged-2.jpg</a> (32.3 KB)</td></tr>
  84. <tr><td><a href="tinywga_All_Paged-3.jpg">tinywga_All_Paged-3.jpg</a> (11.1 KB)</td></tr>
  85. <tr><td><a href="tinywga_All_Paged-4.jpg">tinywga_All_Paged-4.jpg</a> (26.7 KB)</td></tr>
  86. <tr><td><a href="tinywga_All_Paged-5.jpg">tinywga_All_Paged-5.jpg</a> (18.4 KB)</td></tr>
  87. <tr><td><a href="tinywga_All_Paged-6.jpg">tinywga_All_Paged-6.jpg</a> (28.1 KB)</td></tr>
  88. <tr><td><a href="tinywga_All_Paged-7.jpg">tinywga_All_Paged-7.jpg</a> (11.9 KB)</td></tr>
  89. <tr><td><a href="tinywga_All_Paged-8.jpg">tinywga_All_Paged-8.jpg</a> (29.6 KB)</td></tr>
  90. <tr><td><a href="tinywga_All_Paged-9.jpg">tinywga_All_Paged-9.jpg</a> (17.9 KB)</td></tr>
  91. <tr><td><a href="tinywga_All_Paged.pdf">tinywga_All_Paged.pdf</a> (81.9 KB)</td></tr>
  92. <tr><td><a href="tinywga_fracmiss.jpg">tinywga_fracmiss.jpg</a> (12.0 KB)</td></tr>
  93. <tr><td><a href="tinywga_fracmiss.pdf">tinywga_fracmiss.pdf</a> (6.4 KB)</td></tr>
  94. <tr><td><a href="tinywga_fracmiss_cum.jpg">tinywga_fracmiss_cum.jpg</a> (30.0 KB)</td></tr>
  95. <tr><td><a href="tinywga_fracmiss_cum.pdf">tinywga_fracmiss_cum.pdf</a> (7.0 KB)</td></tr>
  96. <tr><td><a href="tinywga_logphweunaff.jpg">tinywga_logphweunaff.jpg</a> (13.6 KB)</td></tr>
  97. <tr><td><a href="tinywga_logphweunaff.pdf">tinywga_logphweunaff.pdf</a> (5.7 KB)</td></tr>
  98. <tr><td><a href="tinywga_logphweunaff_cum.jpg">tinywga_logphweunaff_cum.jpg</a> (26.8 KB)</td></tr>
  99. <tr><td><a href="tinywga_logphweunaff_cum.pdf">tinywga_logphweunaff_cum.pdf</a> (5.8 KB)</td></tr>
  100. <tr><td><a href="tinywga_maf.jpg">tinywga_maf.jpg</a> (18.5 KB)</td></tr>
  101. <tr><td><a href="tinywga_maf.pdf">tinywga_maf.pdf</a> (6.4 KB)</td></tr>
  102. <tr><td><a href="tinywga_maf_cum.jpg">tinywga_maf_cum.jpg</a> (28.5 KB)</td></tr>
  103. <tr><td><a href="tinywga_maf_cum.pdf">tinywga_maf_cum.pdf</a> (6.0 KB)</td></tr>
  104. <tr><td><a href="tinywga_missfrac.jpg">tinywga_missfrac.jpg</a> (11.1 KB)</td></tr>
  105. <tr><td><a href="tinywga_missfrac.pdf">tinywga_missfrac.pdf</a> (5.9 KB)</td></tr>
  106. <tr><td><a href="tinywga_missfrac_cum.jpg">tinywga_missfrac_cum.jpg</a> (27.3 KB)</td></tr>
  107. <tr><td><a href="tinywga_missfrac_cum.pdf">tinywga_missfrac_cum.pdf</a> (5.9 KB)</td></tr>
  108. <tr><td><a href="tinywga_s_het.jpg">tinywga_s_het.jpg</a> (18.0 KB)</td></tr>
  109. <tr><td><a href="tinywga_s_het.pdf">tinywga_s_het.pdf</a> (6.8 KB)</td></tr>
  110. <tr><td><a href="tinywga_s_het_cum.jpg">tinywga_s_het_cum.jpg</a> (31.9 KB)</td></tr>
  111. <tr><td><a href="tinywga_s_het_cum.pdf">tinywga_s_het_cum.pdf</a> (7.3 KB)</td></tr>
  112. </table><h4>QC run log contents</h4><pre>## subject reports starting at 19/05/2010 15:15:38
  113. ## imissfile /opt/galaxy/test-data/rgtestouts/rgQC/tinywga.imiss contained 40 ids
  114. ### writing /opt/galaxy/test-data/rgtestouts/rgQC/SubjectDetails_rgQCtest1.xls report with ['famId', 'iId', 'FracMiss', 'Mendel_errors', 'Ped_sex', 'SNP_sex', 'Status', 'XHomEst', 'F_Stat']## marker reports starting at 19/05/2010 15:15:38
  115. hwe header testpos=2,ppos=8,snppos=1
  116. ## starting plotpage, newfpath=/opt/galaxy/test-data/rgtestouts/rgQC,m=[['snp', 'chromosome', 'offset', 'maf', 'a1', 'a2', 'missfrac', 'p_hwe_all', 'logp_hwe_all', 'p_hwe_unaff', 'logp_hwe_unaff', 'N_Mendel'], ['rs2283802', '22', '21784722', '0.2593', '4', '2', '0', '0.638', '0.195179', '0.638', '0.195179', '0']],s=[['famId', 'iId', 'FracMiss', 'Mendel_errors', 'Ped_sex', 'SNP_sex', 'Status', 'XHomEst', 'F_Stat'], ['101', '1', '0.04', '0', '2', '0', 'PROBLEM', 'nan', '-0.03355']]/n## Rgenetics: http://rgenetics.org Galaxy Tools rgQC.py Plink runner
  117. @----------------------------------------------------------@
  118. | PLINK! | v1.06 | 24/Apr/2009 |
  119. |----------------------------------------------------------|
  120. | (C) 2009 Shaun Purcell, GNU General Public License, v2 |
  121. |----------------------------------------------------------|
  122. | For documentation, citation & bug-report instructions: |
  123. | http://pngu.mgh.harvard.edu/purcell/plink/ |
  124. @----------------------------------------------------------@
  125. Skipping web check... [ --noweb ]
  126. Writing this text to log file [ tinywga.log ]
  127. Analysis started: Wed May 19 15:15:38 2010
  128. Options in effect:
  129. --noweb
  130. --out tinywga
  131. --bfile /opt/galaxy/test-data/tinywga
  132. --mind 1.0
  133. --geno 1.0
  134. --maf 0.0
  135. --freq
  136. Reading map (extended format) from [ /opt/galaxy/test-data/tinywga.bim ]
  137. 25 markers to be included from [ /opt/galaxy/test-data/tinywga.bim ]
  138. Reading pedigree information from [ /opt/galaxy/test-data/tinywga.fam ]
  139. 40 individuals read from [ /opt/galaxy/test-data/tinywga.fam ]
  140. 40 individuals with nonmissing phenotypes
  141. Assuming a disease phenotype (1=unaff, 2=aff, 0=miss)
  142. Missing phenotype value is also -9
  143. 10 cases, 30 controls and 0 missing
  144. 21 males, 19 females, and 0 of unspecified sex
  145. Reading genotype bitfile from [ /opt/galaxy/test-data/tinywga.bed ]
  146. Detected that binary PED file is v1.00 SNP-major mode
  147. Before frequency and genotyping pruning, there are 25 SNPs
  148. 27 founders and 13 non-founders found
  149. Writing allele frequencies (founders-only) to [ tinywga.frq ]
  150. Analysis finished: Wed May 19 15:15:38 2010
  151. @----------------------------------------------------------@
  152. | PLINK! | v1.06 | 24/Apr/2009 |
  153. |----------------------------------------------------------|
  154. | (C) 2009 Shaun Purcell, GNU General Public License, v2 |
  155. |----------------------------------------------------------|
  156. | For documentation, citation & bug-report instructions: |
  157. | http://pngu.mgh.harvard.edu/purcell/plink/ |
  158. @----------------------------------------------------------@
  159. Skipping web check... [ --noweb ]
  160. Writing this text to log file [ tinywga.log ]
  161. Analysis started: Wed May 19 15:15:38 2010
  162. Options in effect:
  163. --noweb
  164. --out tinywga
  165. --bfile /opt/galaxy/test-data/tinywga
  166. --mind 1.0
  167. --geno 1.0
  168. --maf 0.0
  169. --hwe 0.0
  170. --missing
  171. --hardy
  172. Reading map (extended format) from [ /opt/galaxy/test-data/tinywga.bim ]
  173. 25 markers to be included from [ /opt/galaxy/test-data/tinywga.bim ]
  174. Reading pedigree information from [ /opt/galaxy/test-data/tinywga.fam ]
  175. 40 individuals read from [ /opt/galaxy/test-data/tinywga.fam ]
  176. 40 individuals with nonmissing phenotypes
  177. Assuming a disease phenotype (1=unaff, 2=aff, 0=miss)
  178. Missing phenotype value is also -9
  179. 10 cases, 30 controls and 0 missing
  180. 21 males, 19 females, and 0 of unspecified sex
  181. Reading genotype bitfile from [ /opt/galaxy/test-data/tinywga.bed ]
  182. Detected that binary PED file is v1.00 SNP-major mode
  183. Before frequency and genotyping pruning, there are 25 SNPs
  184. 27 founders and 13 non-founders found
  185. Writing Hardy-Weinberg tests (founders-only) to [ tinywga.hwe ]
  186. 0 markers to be excluded based on HWE test ( p <= 0 )
  187. 0 markers failed HWE test in cases
  188. 0 markers failed HWE test in controls
  189. Writing individual missingness information to [ tinywga.imiss ]
  190. Writing locus missingness information to [ tinywga.lmiss ]
  191. Total genotyping rate in remaining individuals is 0.995
  192. 0 SNPs failed missingness test ( GENO > 1 )
  193. 0 SNPs failed frequency test ( MAF < 0 )
  194. After frequency and genotyping pruning, there are 25 SNPs
  195. After filtering, 10 cases, 30 controls and 0 missing
  196. After filtering, 21 males, 19 females, and 0 of unspecified sex
  197. Analysis finished: Wed May 19 15:15:38 2010
  198. @----------------------------------------------------------@
  199. | PLINK! | v1.06 | 24/Apr/2009 |
  200. |----------------------------------------------------------|
  201. | (C) 2009 Shaun Purcell, GNU General Public License, v2 |
  202. |----------------------------------------------------------|
  203. | For documentation, citation & bug-report instructions: |
  204. | http://pngu.mgh.harvard.edu/purcell/plink/ |
  205. @----------------------------------------------------------@
  206. Skipping web check... [ --noweb ]
  207. Writing this text to log file [ tinywga.log ]
  208. Analysis started: Wed May 19 15:15:38 2010
  209. Options in effect:
  210. --noweb
  211. --out tinywga
  212. --bfile /opt/galaxy/test-data/tinywga
  213. --mind 1.0
  214. --geno 1.0
  215. --maf 0.0
  216. --mendel
  217. Reading map (extended format) from [ /opt/galaxy/test-data/tinywga.bim ]
  218. 25 markers to be included from [ /opt/galaxy/test-data/tinywga.bim ]
  219. Reading pedigree information from [ /opt/galaxy/test-data/tinywga.fam ]
  220. 40 individuals read from [ /opt/galaxy/test-data/tinywga.fam ]
  221. 40 individuals with nonmissing phenotypes
  222. Assuming a disease phenotype (1=unaff, 2=aff, 0=miss)
  223. Missing phenotype value is also -9
  224. 10 cases, 30 controls and 0 missing
  225. 21 males, 19 females, and 0 of unspecified sex
  226. Reading genotype bitfile from [ /opt/galaxy/test-data/tinywga.bed ]
  227. Detected that binary PED file is v1.00 SNP-major mode
  228. Before frequency and genotyping pruning, there are 25 SNPs
  229. 27 founders and 13 non-founders found
  230. Total genotyping rate in remaining individuals is 0.995
  231. 0 SNPs failed missingness test ( GENO > 1 )
  232. 0 SNPs failed frequency test ( MAF < 0 )
  233. After frequency and genotyping pruning, there are 25 SNPs
  234. After filtering, 10 cases, 30 controls and 0 missing
  235. After filtering, 21 males, 19 females, and 0 of unspecified sex
  236. 14 nuclear families, 1 founder singletons found
  237. 13 non-founders with 2 parents in 13 nuclear families
  238. 0 non-founders without 2 parents in 0 nuclear families
  239. 10 affected offspring trios
  240. 0 phenotypically discordant parent pairs found
  241. Converting data to Individual-major format
  242. Writing all Mendel errors to [ tinywga.mendel ]
  243. Writing per-offspring Mendel summary to [ tinywga.imendel ]
  244. Writing per-family Mendel summary to [ tinywga.fmendel ]
  245. Writing per-locus Mendel summary to [ tinywga.lmendel ]
  246. 0 Mendel errors detected in total
  247. Analysis finished: Wed May 19 15:15:38 2010
  248. @----------------------------------------------------------@
  249. | PLINK! | v1.06 | 24/Apr/2009 |
  250. |----------------------------------------------------------|
  251. | (C) 2009 Shaun Purcell, GNU General Public License, v2 |
  252. |----------------------------------------------------------|
  253. | For documentation, citation & bug-report instructions: |
  254. | http://pngu.mgh.harvard.edu/purcell/plink/ |
  255. @----------------------------------------------------------@
  256. Skipping web check... [ --noweb ]
  257. Writing this text to log file [ tinywga.log ]
  258. Analysis started: Wed May 19 15:15:38 2010
  259. Options in effect:
  260. --noweb
  261. --out tinywga
  262. --bfile /opt/galaxy/test-data/tinywga
  263. --mind 1.0
  264. --geno 1.0
  265. --maf 0.0
  266. --check-sex
  267. Reading map (extended format) from [ /opt/galaxy/test-data/tinywga.bim ]
  268. 25 markers to be included from [ /opt/galaxy/test-data/tinywga.bim ]
  269. Reading pedigree information from [ /opt/galaxy/test-data/tinywga.fam ]
  270. 40 individuals read from [ /opt/galaxy/test-data/tinywga.fam ]
  271. 40 individuals with nonmissing phenotypes
  272. Assuming a disease phenotype (1=unaff, 2=aff, 0=miss)
  273. Missing phenotype value is also -9
  274. 10 cases, 30 controls and 0 missing
  275. 21 males, 19 females, and 0 of unspecified sex
  276. Reading genotype bitfile from [ /opt/galaxy/test-data/tinywga.bed ]
  277. Detected that binary PED file is v1.00 SNP-major mode
  278. Before frequency and genotyping pruning, there are 25 SNPs
  279. 27 founders and 13 non-founders found
  280. Total genotyping rate in remaining individuals is 0.995
  281. 0 SNPs failed missingness test ( GENO > 1 )
  282. 0 SNPs failed frequency test ( MAF < 0 )
  283. After frequency and genotyping pruning, there are 25 SNPs
  284. After filtering, 10 cases, 30 controls and 0 missing
  285. After filtering, 21 males, 19 females, and 0 of unspecified sex
  286. Converting data to Individual-major format
  287. Writing X-chromosome sex check results to [ tinywga.sexcheck ]
  288. Analysis finished: Wed May 19 15:15:38 2010
  289. ## Rgenetics: http://rgenetics.org Galaxy Tools rgQC.py Plink pruneLD runner
  290. @----------------------------------------------------------@
  291. | PLINK! | v1.06 | 24/Apr/2009 |
  292. |----------------------------------------------------------|
  293. | (C) 2009 Shaun Purcell, GNU General Public License, v2 |
  294. |----------------------------------------------------------|
  295. | For documentation, citation & bug-report instructions: |
  296. | http://pngu.mgh.harvard.edu/purcell/plink/ |
  297. @----------------------------------------------------------@
  298. Skipping web check... [ --noweb ]
  299. Writing this text to log file [ tinywga.log ]
  300. Analysis started: Wed May 19 15:15:38 2010
  301. Options in effect:
  302. --noweb
  303. --bfile /opt/galaxy/test-data/tinywga
  304. --indep-pairwise 40 20 0.5
  305. --out tinywga
  306. Reading map (extended format) from [ /opt/galaxy/test-data/tinywga.bim ]
  307. 25 markers to be included from [ /opt/galaxy/test-data/tinywga.bim ]
  308. Reading pedigree information from [ /opt/galaxy/test-data/tinywga.fam ]
  309. 40 individuals read from [ /opt/galaxy/test-data/tinywga.fam ]
  310. 40 individuals with nonmissing phenotypes
  311. Assuming a disease phenotype (1=unaff, 2=aff, 0=miss)
  312. Missing phenotype value is also -9
  313. 10 cases, 30 controls and 0 missing
  314. 21 males, 19 females, and 0 of unspecified sex
  315. Reading genotype bitfile from [ /opt/galaxy/test-data/tinywga.bed ]
  316. Detected that binary PED file is v1.00 SNP-major mode
  317. Before frequency and genotyping pruning, there are 25 SNPs
  318. 27 founders and 13 non-founders found
  319. Total genotyping rate in remaining individuals is 0.995
  320. 0 SNPs failed missingness test ( GENO > 1 )
  321. 0 SNPs failed frequency test ( MAF < 0 )
  322. After frequency and genotyping pruning, there are 25 SNPs
  323. After filtering, 10 cases, 30 controls and 0 missing
  324. After filtering, 21 males, 19 females, and 0 of unspecified sex
  325. Performing LD-based pruning...
  326. Writing pruned-in SNPs to [ tinywga.prune.in ]
  327. Writing pruned-out SNPs to [ tinywga.prune.out ]
  328. Scanning from chromosome 22 to 22
  329. Scan region on chromosome 22 from [ rs2283802 ] to [ rs4822375 ]
  330. For chromosome 22, 11 SNPs pruned out, 14 remaining
  331. Analysis finished: Wed May 19 15:15:38 2010
  332. @----------------------------------------------------------@
  333. | PLINK! | v1.06 | 24/Apr/2009 |
  334. |----------------------------------------------------------|
  335. | (C) 2009 Shaun Purcell, GNU General Public License, v2 |
  336. |----------------------------------------------------------|
  337. | For documentation, citation & bug-report instructions: |
  338. | http://pngu.mgh.harvard.edu/purcell/plink/ |
  339. @----------------------------------------------------------@
  340. Skipping web check... [ --noweb ]
  341. Writing this text to log file [ ldp_tinywga.log ]
  342. Analysis started: Wed May 19 15:15:38 2010
  343. Options in effect:
  344. --noweb
  345. --bfile /opt/galaxy/test-data/tinywga
  346. --extract tinywga.prune.in
  347. --make-bed
  348. --out ldp_tinywga
  349. Reading map (extended format) from [ /opt/galaxy/test-data/tinywga.bim ]
  350. 25 markers to be included from [ /opt/galaxy/test-data/tinywga.bim ]
  351. Reading pedigree information from [ /opt/galaxy/test-data/tinywga.fam ]
  352. 40 individuals read from [ /opt/galaxy/test-data/tinywga.fam ]
  353. 40 individuals with nonmissing phenotypes
  354. Assuming a disease phenotype (1=unaff, 2=aff, 0=miss)
  355. Missing phenotype value is also -9
  356. 10 cases, 30 controls and 0 missing
  357. 21 males, 19 females, and 0 of unspecified sex
  358. Reading genotype bitfile from [ /opt/galaxy/test-data/tinywga.bed ]
  359. Detected that binary PED file is v1.00 SNP-major mode
  360. Reading list of SNPs to extract [ tinywga.prune.in ] ... 14 read
  361. Before frequency and genotyping pruning, there are 14 SNPs
  362. 27 founders and 13 non-founders found
  363. Total genotyping rate in remaining individuals is 0.991071
  364. 0 SNPs failed missingness test ( GENO > 1 )
  365. 0 SNPs failed frequency test ( MAF < 0 )
  366. After frequency and genotyping pruning, there are 14 SNPs
  367. After filtering, 10 cases, 30 controls and 0 missing
  368. After filtering, 21 males, 19 females, and 0 of unspecified sex
  369. Writing pedigree information to [ ldp_tinywga.fam ]
  370. Writing map (extended format) information to [ ldp_tinywga.bim ]
  371. Writing genotype bitfile to [ ldp_tinywga.bed ]
  372. Using (default) SNP-major mode
  373. Analysis finished: Wed May 19 15:15:38 2010
  374. @----------------------------------------------------------@
  375. | PLINK! | v1.06 | 24/Apr/2009 |
  376. |----------------------------------------------------------|
  377. | (C) 2009 Shaun Purcell, GNU General Public License, v2 |
  378. |----------------------------------------------------------|
  379. | For documentation, citation & bug-report instructions: |
  380. | http://pngu.mgh.harvard.edu/purcell/plink/ |
  381. @----------------------------------------------------------@
  382. Skipping web check... [ --noweb ]
  383. Writing this text to log file [ tinywga.log ]
  384. Analysis started: Wed May 19 15:15:38 2010
  385. Options in effect:
  386. --noweb
  387. --bfile ldp_tinywga
  388. --het
  389. --out tinywga
  390. Reading map (extended format) from [ ldp_tinywga.bim ]
  391. 14 markers to be included from [ ldp_tinywga.bim ]
  392. Reading pedigree information from [ ldp_tinywga.fam ]
  393. 40 individuals read from [ ldp_tinywga.fam ]
  394. 40 individuals with nonmissing phenotypes
  395. Assuming a disease phenotype (1=unaff, 2=aff, 0=miss)
  396. Missing phenotype value is also -9
  397. 10 cases, 30 controls and 0 missing
  398. 21 males, 19 females, and 0 of unspecified sex
  399. Reading genotype bitfile from [ ldp_tinywga.bed ]
  400. Detected that binary PED file is v1.00 SNP-major mode
  401. Before frequency and genotyping pruning, there are 14 SNPs
  402. 27 founders and 13 non-founders found
  403. Total genotyping rate in remaining individuals is 0.991071
  404. 0 SNPs failed missingness test ( GENO > 1 )
  405. 0 SNPs failed frequency test ( MAF < 0 )
  406. After frequency and genotyping pruning, there are 14 SNPs
  407. After filtering, 10 cases, 30 controls and 0 missing
  408. After filtering, 21 males, 19 females, and 0 of unspecified sex
  409. **Warning** this analysis typically requires whole-genome level data
  410. to give accurate results
  411. Converting data to Individual-major format
  412. Writing individual heterozygosity information to [ tinywga.het ]
  413. Analysis finished: Wed May 19 15:15:38 2010
  414. </pre></div></body></html>
  415. <hr>