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[Update] documentation
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choishingwan committed May 19, 2020
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13 changes: 10 additions & 3 deletions docs/index.md
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Expand Up @@ -18,13 +18,20 @@ PRSice (pronounced 'precise') is a Polygenic Risk Score software for calculating
# Executable downloads [![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.3703335.svg)](https://doi.org/10.5281/zenodo.3703335)[![Coverage Status](https://coveralls.io/repos/github/choishingwan/PRSice/badge.svg?branch=master)](https://coveralls.io/github/choishingwan/PRSice?branch=master)
| Operating System | Link |
| -----------------|:----:|
| Linux 64-bit | [v2.3.0](https://github.com/choishingwan/PRSice/releases/download/2.3.0/PRSice_linux.zip) |
| OS X 64-bit | [v2.3.0](https://github.com/choishingwan/PRSice/releases/download/2.3.0/PRSice_mac.zip) |
| Linux 64-bit | [v2.3.0.a](https://github.com/choishingwan/PRSice/releases/download/2.3.0.a/PRSice_linux.zip) |
| OS X 64-bit | [v2.3.0.a](https://github.com/choishingwan/PRSice/releases/download/2.3.0.a/PRSice_mac.zip) |
| Windows 32-bit | Not available |
| Windows 64-bit | Not available |

!!! Note "Latest Update"


# 2020-05-19
- Fix output error where we always say 0 valid phenotype were included for continuous trait
- Fix problem with permutation where PRSice will crash if input are rank deficient
- Fix problem when provide a binary phenotype file with a fam file containing -9 as phenotype, PRSice will wrongly state that there are no phenotype presented
- Fix problem in Rscript where if sample ID is numeric and starts with 0, the best file will not merge with the phenotype file, causing 0 valid PRS to be observed

# 2020-05-18
- We now support multi-threaded clumping (separated by chromosome)
- Genotypes will be stored to memory during clumping (increase memory usage, significantly speed up clumping)
- Will only generate one .prsice file for all phenotypes
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9 changes: 7 additions & 2 deletions docs/update_log.md
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From now on, I will try to archive our update log here.

# 2020-05-19 ([v2.3.0.a](https://github.com/choishingwan/PRSice/tree/87c8571f8b27d39cfe6d8ec3b00e059d0ecf0376))
- Fix output error where we always say 0 valid phenotype were included for continuous trait
- Fix problem with permutation where PRSice will crash if input are rank deficient
- Fix problem when provide a binary phenotype file with a fam file containing -9 as phenotype, PRSice will wrongly state that there are no phenotype presented
- Fix problem in Rscript where if sample ID is numeric and starts with 0, the best file will not merge with the phenotype file, causing 0 valid PRS to be observed

# 2020-05-18 (v2.3.0)
# 2020-05-18 ([v2.3.0](https://github.com/choishingwan/PRSice/tree/2.3.0))
- We now support multi-threaded clumping (separated by chromosome)
- Genotypes will be stored to memory during clumping (increase memory usage, significantly speed up clumping)
- Will only generate one .prsice file for all phenotypes
Expand All @@ -13,4 +18,4 @@ From now on, I will try to archive our update log here.
- Fix bug in 2.2.13 where PRSice won't output the error message during command parsing stage
- If user provided the `--stat` information, PRSice will now error out instead of trying to look for BETA or OR in the file.
- PRSice should now better recognize if phenotype file contains a header
- various small bug fix
- various small bug fix

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