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Merge pull request #419 from satijalab/release/3.2.2
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Prep for CRAN release of 3.2.2
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mojaveazure authored Sep 25, 2020
2 parents 0f59a40 + 1b3967a commit 7c7423d
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4 changes: 2 additions & 2 deletions DESCRIPTION
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Package: Seurat
Version: 3.2.1.9005
Date: 2020-09-21
Version: 3.2.2
Date: 2020-09-25
Title: Tools for Single Cell Genomics
Description: A toolkit for quality control, analysis, and exploration of single cell RNA sequencing data. 'Seurat' aims to enable users to identify and interpret sources of heterogeneity from single cell transcriptomic measurements, and to integrate diverse types of single cell data. See Satija R, Farrell J, Gennert D, et al (2015) <doi:10.1038/nbt.3192>, Macosko E, Basu A, Satija R, et al (2015) <doi:10.1016/j.cell.2015.05.002>, and Stuart T, Butler A, et al (2019) <doi:10.1016/j.cell.2019.05.031> for more details.
Authors@R: c(
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4 changes: 1 addition & 3 deletions NEWS.md
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All notable changes to Seurat will be documented in this file.
The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.0.0/)

## [unreleased]
### Added

## [3.2.2] - 2020-09-25
### Changes
- Set the seed in `WhichCells` regardless of whether or not `idents` is passed
- Retain Graph and Neighbor objects when subsetting only on features
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2 changes: 1 addition & 1 deletion README.md
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[![CRAN Version](https://www.r-pkg.org/badges/version/Seurat)](https://cran.r-project.org/package=Seurat)
[![CRAN Downloads](https://cranlogs.r-pkg.org/badges/Seurat)](https://cran.r-project.org/package=Seurat)

# Seurat v3.2.1
# Seurat v3.2.2


Seurat is an R toolkit for single cell genomics, developed and maintained by the Satija Lab at NYGC.
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2 changes: 1 addition & 1 deletion cran-comments.md
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# Seurat v3.2.0
# Seurat v3.2.2

## Test environments
* local Ubuntu 16.04.6 install, R 3.6.1
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