User Tools
Differences
This shows you the differences between two versions of the page.
| — |
sidebar [2016/04/13 18:02] (current) |
||
|---|---|---|---|
| Line 1: | Line 1: | ||
| + | ~~NOCACHE~~ | ||
| + | |||
| + | * **[[start|About]]** | ||
| + | * [[installation|Installation]] | ||
| + | * [[support|Support]] | ||
| + | * [[changelog|Version History]] | ||
| + | |||
| + | * **[[docs|Documentation]]** | ||
| + | * [[options|Command Interface]] | ||
| + | * [[empirical|Empirical Power Analysis]] | ||
| + | * [[melnr|Extreme Quantitative Traits Model]] | ||
| + | * [[srvbatch|Forward-time Simulation with SRV]] | ||
| + | * [[mblnr|Linear Model Binary Outcome]] | ||
| + | * [[mlnr|Linear Model Quantitative Traits]] | ||
| + | * [[mlogit|Logit Model Binary Outcome]] | ||
| + | * [[mpar|Population Attributable Risk Model]] | ||
| + | * [[cc|Power for Case Control Studies]] | ||
| + | * [[qt|Power for Quantitative Traits]] | ||
| + | * [[vat-methods|Rare Variant Association Methods]] | ||
| + | * [[input|SEQPower Input]] | ||
| + | * [[output|SEQPower Output]] | ||
| + | * [[vat-r|SEQPower R Interface]] | ||
| + | * [[simtraits|Simulating Genetic Associations]] | ||
| + | * [[simseq|Simulation of DNA Sequence Data]] | ||
| + | * [[allargs|Table of Command Options]] | ||
| + | * [[write|Write Simulation Data Set to Files]] | ||
| + | |||
| + | * **[[tutorial|Tutorial]]** | ||
| + | * [[quickstart|A Quick Start Tutorial]] | ||
| + | * [[analytic-tutorial|Analytic Power Analysis]] | ||
| + | * [[dataset|EVS Data Derived Haplotype Pool]] | ||
| + | * [[empirical-tutorial|Empirical Power Analysis]] | ||
| + | * [[artifact|Emulating Genotyping Artifact]] | ||
| + | * [[benchmark|SEQPower Benchmark]] | ||
| + | * [[srvbatch-tutorial|Simulate Rare Variants Data]] | ||
