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, 13:03, 12 September 2013
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| #Variant Annotations using [[VcfCodingSnps]] | | #Variant Annotations using [[VcfCodingSnps]] |
| #Rare Variant Analysis using [[RvTests]] | | #Rare Variant Analysis using [[RvTests]] |
| + | #Rare Variant Association Analysis in family samples [[FamRvTest]] |
| #Quality control using [[C++ Executable: fastQValidator|FastQValidator]], [[VerifyBamID]], and [[BamValidator]] | | #Quality control using [[C++ Executable: fastQValidator|FastQValidator]], [[VerifyBamID]], and [[BamValidator]] |
| #C++ APIs for sequence analsysis using [[C++ Library: libStatGen]] | | #C++ APIs for sequence analsysis using [[C++ Library: libStatGen]] |
| #Meta-analysis of single variant or gene-level associations, including tools for generating summary statistics ([[Rvtests]],[[RAREMETALWORKER]]), annotating summary statistics ([[TabAnno]]), and performing meta-analysis (command line tool [[RAREMETAL]] and R package [[RareMETALS]]). | | #Meta-analysis of single variant or gene-level associations, including tools for generating summary statistics ([[Rvtests]],[[RAREMETALWORKER]]), annotating summary statistics ([[TabAnno]]), and performing meta-analysis (command line tool [[RAREMETAL]] and R package [[RareMETALS]]). |
| + | #Sequencing study design helper [[Rarefy]] |
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| These tools and additional tools can be found on the [[Software]] page. | | These tools and additional tools can be found on the [[Software]] page. |