Biostatistics 830 - Code Snippets: Difference between revisions

From Genome Analysis Wiki
Jump to navigationJump to search
 
(27 intermediate revisions by the same user not shown)
Line 8: Line 8:


[[830 - Haplotyper::RandomSetup()]]
[[830 - Haplotyper::RandomSetup()]]
[[830 - Haplotyper::SetupPrior()]]
[[830 - Haplotyper::Transpose()]]
[[830 - Haplotyper::ConditionOnData()]]
[[830 - Haplotyper::ScoreLeftConditional()]]
[[830 - Haplotyper::ScoreLeftConditional() (smart, complicated)]]
[[830 - Haplotyper::SampleChromosomes()]]
[[830 - Haplotyper::SampleHaplotypes()]]
[[830 - Haplotyper::SummarizeOptions()]]
[[830 - Haplotyper::SampleOneHaplotype()]]
[[830 - Haplotyper::ImputeGenotypes()]]
[[830 - Haplotyper::ImputeGenotypes() (edge)]]
[[830 - Haplotyper::ImputeGenotypes() (internal)]]
== Howie et al (2012) Nat Genet ==
=== Full Citation ===
Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR (2012) Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. ''Nat Genet.'' '''44''':955-9. PMID: 22820512
=== Code Snippets ===
[[830 - MarkovModel::Transpose()]]
[[830 - MarkovModel::Condition()]]
[[830 - MarkovModel::WalkLeft()]]
[[830 - MarkovModel::WalkRight()]]
[[830 - MarkovModel::Impute()]]
[[830 - MarkovModel::CountRecombinants()]]
[[830 - MarkovModel::CountErrors()]]
[[830 - MarkovModel::CountErrorsAndRecombinants()]]
[[830 - MINIMAC::main()]]
== Li et al (2013) Genome Research ==
=== Full Citation ===
Li H, Ruan J, Durbin R (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. ''Genome Res.'' '''18''':1851-8.
=== Code Snippets ===
[[830 - BasicMapper::main()]]
[[830 - MaqIndex::GetWord()]]
[[830 - MaqIndex::BuildIndex()]]
[[830 - MaqIndex::LookupWord()]]
[[830 - MaqIndex::CompareToIndex()]]
[[830 - BestAlignment::MaqAlignment()]]
[[830 - BestAlignment::EvaluateAlignment() (main loop)]]
[[830 - BestAlignment::EvaluateAlignment() (detailed comparison)]]
[[830 - BestAlignment::isNewPosition()]]
[[830 - BestAlignment::IterateCache()]]
[[830 - BestAlignment::ClearPositions()]]

Latest revision as of 13:53, 28 October 2013

Li et al (2010) Genet Epidemiol

Full Citation

Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR (2010) MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol. 34:816-34

Code Snippets

830 - Haplotyper::RandomSetup()

830 - Haplotyper::SetupPrior()

830 - Haplotyper::Transpose()

830 - Haplotyper::ConditionOnData()

830 - Haplotyper::ScoreLeftConditional()

830 - Haplotyper::ScoreLeftConditional() (smart, complicated)

830 - Haplotyper::SampleChromosomes()

830 - Haplotyper::SampleHaplotypes()

830 - Haplotyper::SummarizeOptions()

830 - Haplotyper::SampleOneHaplotype()

830 - Haplotyper::ImputeGenotypes()

830 - Haplotyper::ImputeGenotypes() (edge)

830 - Haplotyper::ImputeGenotypes() (internal)

Howie et al (2012) Nat Genet

Full Citation

Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR (2012) Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat Genet. 44:955-9. PMID: 22820512

Code Snippets

830 - MarkovModel::Transpose()

830 - MarkovModel::Condition()

830 - MarkovModel::WalkLeft()

830 - MarkovModel::WalkRight()

830 - MarkovModel::Impute()

830 - MarkovModel::CountRecombinants()

830 - MarkovModel::CountErrors()

830 - MarkovModel::CountErrorsAndRecombinants()

830 - MINIMAC::main()

Li et al (2013) Genome Research

Full Citation

Li H, Ruan J, Durbin R (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res. 18:1851-8.

Code Snippets

830 - BasicMapper::main()

830 - MaqIndex::GetWord()

830 - MaqIndex::BuildIndex()

830 - MaqIndex::LookupWord()

830 - MaqIndex::CompareToIndex()

830 - BestAlignment::MaqAlignment()

830 - BestAlignment::EvaluateAlignment() (main loop)

830 - BestAlignment::EvaluateAlignment() (detailed comparison)

830 - BestAlignment::isNewPosition()

830 - BestAlignment::IterateCache()

830 - BestAlignment::ClearPositions()