Dead-end pages

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Showing below up to 211 results in range #1 to #211.

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  1. 1000 Genomes Project Pilot 1 SNP Calling
  2. 830 - BasicMapper::main()
  3. 830 - BestAlignment::ClearPositions()
  4. 830 - BestAlignment::EvaluateAlignment() (detailed comparison)
  5. 830 - BestAlignment::EvaluateAlignment() (main loop)
  6. 830 - BestAlignment::IterateCache()
  7. 830 - BestAlignment::MaqAlignment()
  8. 830 - BestAlignment::isNewPosition()
  9. 830 - Haplotyper::ConditionOnData()
  10. 830 - Haplotyper::ImputeGenotypes()
  11. 830 - Haplotyper::ImputeGenotypes() (edge)
  12. 830 - Haplotyper::ImputeGenotypes() (internal)
  13. 830 - Haplotyper::RandomSetup()
  14. 830 - Haplotyper::SampleChromosomes()
  15. 830 - Haplotyper::SampleHaplotypes()
  16. 830 - Haplotyper::SampleOneHaplotype()
  17. 830 - Haplotyper::ScoreLeftConditional()
  18. 830 - Haplotyper::ScoreLeftConditional() (smart, complicated)
  19. 830 - Haplotyper::SetupPrior()
  20. 830 - Haplotyper::SummarizeOptions()
  21. 830 - Haplotyper::Transpose()
  22. 830 - MINIMAC::main()
  23. 830 - MaqIndex::BuildIndex()
  24. 830 - MaqIndex::CompareToIndex()
  25. 830 - MaqIndex::GetWord()
  26. 830 - MaqIndex::LookupWord()
  27. 830 - MarkovModel::Condition()
  28. 830 - MarkovModel::CountErrors()
  29. 830 - MarkovModel::CountErrorsAndRecombinants()
  30. 830 - MarkovModel::CountRecombinants()
  31. 830 - MarkovModel::Impute()
  32. 830 - MarkovModel::Transpose()
  33. 830 - MarkovModel::WalkLeft()
  34. 830 - MarkovModel::WalkRight()
  35. Abecasis Group Awards
  36. An example of using libcsg
  37. Ancestry
  38. Ann Arbor Travel Basics
  39. BAFRegress
  40. BAM Review Action Items
  41. BamPileup
  42. Bam read count
  43. BaseQualityCheck
  44. Base Caller Summaries
  45. Basic Linux Intro
  46. Bayesdenovo
  47. Better X Sessions from Home (NX)
  48. Biostatistics 602: Main Page
  49. Biostatistics 666: Advanced Coalescent, Changing Population Size
  50. Biostatistics 666: Advanced Coalescent, Computation with the Coalescent
  51. Biostatistics 666: Advanced Haplotype Estimation
  52. Biostatistics 666: Analysis of Copy Number Using Sequence Data
  53. Biostatistics 666: Analysis of Low Pass Sequence Data
  54. Biostatistics 666: Applications of the Lander-Green Algorithm
  55. Biostatistics 666: Association Tests in Structured Populations
  56. Biostatistics 666: Contemporary Human Genetics
  57. Biostatistics 666: Copy Number Variation
  58. Biostatistics 666: Genotype Imputation
  59. Biostatistics 666: Haplotype Association Tests
  60. Biostatistics 666: Haplotype Estimation
  61. Biostatistics 666: Hardy-Weinberg Equilibrium
  62. Biostatistics 666: Introduction to De Novo Assembly
  63. Biostatistics 666: Introduction to the Coalescent
  64. Biostatistics 666: Introduction to the E-M Algorithm
  65. Biostatistics 666: Introductory Lecture
  66. Biostatistics 666: Likelihood Calculations for Large Pedigrees
  67. Biostatistics 666: Linkage Analysis in Sibling Pairs
  68. Biostatistics 666: Linkage Disequilibrium
  69. Biostatistics 666: Linkage Tests for Pairs of Individuals
  70. Biostatistics 666: Maximum Likelihood Allele Frequency Estimation
  71. Biostatistics 666: Modeling Recombination and Migration in the Coalescent
  72. Biostatistics 666: Modeling Variation in the Coalescent
  73. Biostatistics 666: Multipoint Analysis in Sibling Pairs
  74. Biostatistics 666: Rare Variant Burden Tests
  75. Biostatistics 666: Relationship Checking
  76. Biostatistics 666: The Lander-Green Algorithm
  77. Biostatistics 666: The Possible Triangle Constraint
  78. Biostatistics 666: Variance Component Analyses
  79. Biostatistics 666: Whole Genome Sequencing
  80. Biostatistics 815 Term Project
  81. C++ Class: InputFile
  82. C++ Class: Pedigree Example
  83. C++ Class Averages
  84. CHARGE
  85. CSG Tech Talks
  86. CalcMatch
  87. CheckVCF.py
  88. CigarRoller Proposed Update
  89. Code Sample: Generating Manhattan Plots in R
  90. Code Sample: Generating QQ Plots in R
  91. Dosage convertor
  92. Editing Sequence Analysis Practice 2011/03/10
  93. Evaluating a Read Mapper on Simulated Data
  94. Example
  95. Examples of Read Mapping with Karma and BWA
  96. ExomePicks
  97. FASTA
  98. FamRvTest tutorial
  99. Fst
  100. GREGOR
  101. GTDT
  102. GWAS
  103. Garlic
  104. Gene Ontology
  105. Genezoom
  106. Git Cheat Sheet
  107. Goncalo Abecasis: Interview with Christiana Fogg
  108. GotCloud: AMIs
  109. GotCloud: Creating a New Pipeline
  110. Gzip File
  111. HAPMIX
  112. Haploxt
  113. Hardy Weinberg equilibrium
  114. How to use aspera
  115. IGFPipe
  116. IMPUTE2
  117. Idriver
  118. Imputation Server: Example
  119. Indel
  120. Installing MinGW & MSYS on Windows
  121. Jennifer Bragg-Gresham
  122. Karma
  123. Karma-colorspace
  124. Kyoto Encyclopedia of Genes and Genomes
  125. LASER
  126. Lars Fritsche
  127. LibStatGen: ASP
  128. LibStatGen: GLF
  129. LibStatGen: VCF
  130. LibStatGen Troubleshooting
  131. LiftMap.py
  132. LiftRsNumber.py
  133. Ligate Minimac
  134. MEAGA
  135. MERLIN format
  136. METAL ADDFILTER
  137. METAL COLUMNCOUNTING
  138. METAL CUSTOMVARIABLE
  139. METAL EFFECTLABEL
  140. METAL GENOMICCONTROL
  141. METAL Glucose Example Script
  142. METAL LOGPVALUE
  143. METAL SOURCE
  144. MaCH: Pedigree with Integer Allele Codes
  145. MaCH FAQ
  146. MaCH Options
  147. Mach2dat: Association with MACH output
  148. Make file tutorial
  149. Makefile.tool
  150. MappabilityScores
  151. Merlin
  152. MetaMinimac
  153. MutationFilter
  154. NHLBI Exome Sequencing Project
  155. Outcomes For Mapping A Paired End
  156. PedScript
  157. PhoneHome
  158. Phred scale
  159. Pileup
  160. PileupBasedVariantCalling
  161. Polymutt2
  162. Polymutt beta
  163. Power Calculations: Quantitative Traits
  164. QPLOT
  165. RAREFY FAQ
  166. RAREMETALWORKER X
  167. Rare-metal-worker
  168. RareMETALS
  169. RareMETALS2
  170. RareMetals
  171. RareSimu
  172. Rare variant tests
  173. Regions of high linkage disequilibrium (LD)
  174. Relationship between Ploidy, Alleles and Genotypes
  175. Rvtests
  176. SAM: Filtering Reads
  177. Samtools-hybrid
  178. SardiNIA
  179. SardiNIA project meeting July 15-16, 2013
  180. Sayantan Das
  181. Screen Commands
  182. Sean Caron
  183. SeqShop: Aligning Your Own Genome, December 2014
  184. SeqShop: Aligning Your Own Genome, May 2015
  185. Sequence Analysis Practice 2011/03/09
  186. SplitRef
  187. TOPMed Site Visit 2018
  188. TabAnno
  189. Tandem Repeat Concepts
  190. Test EPACTS for DIAGRAM
  191. Thunder
  192. TinySimulator
  193. Tom Blackwell
  194. Tramp
  195. Trial Enrichment
  196. TrioCaller:Archive
  197. Triodenovo
  198. Tutorial: EMMAX GotCloud STOM: Lecture 2
  199. Tutorial: EMMAX GotCloud STOM: Lecture 6
  200. Tutorial: EMMAX GotCloud STOM: Lecture 8
  201. Tutorial: Low Pass Sequence Analysis Answers
  202. UMAKE-glfSingle
  203. Variant Call Pipeline
  204. Variant Normalization
  205. Variant classification
  206. Vcf2geno
  207. VcfGenomeStat
  208. VcfRefGen
  209. Verifying Sample Identities - Implementation
  210. Vpeep
  211. Xiaowei Zhan

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