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README.md

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-QUILT2
+QUILT2: genotype calling from low coverage reads
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+![Build Status](https://github.com/rwdavies/QUILT/workflows/CI/badge.svg)
+[![install with bioconda](https://img.shields.io/badge/install%20with-bioconda-brightgreen.svg?style=flat)](http://bioconda.github.io/recipes/r-quilt/README.html)
+![](https://anaconda.org/bioconda/r-quilt/badges/version.svg)
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 **__Current Version: 2.0.0__**
 ***Prerelease*** date: July 06, 2024
 
-![Build Status](https://github.com/rwdavies/QUILT/workflows/CI/badge.svg)
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 We are excited to release QUILT2, a major upgrade over QUILT (QUILT1). For details of past changes to QUILT2 and QUILT1, please see the [CHANGELOG](CHANGELOG.md).
 
 QUILT2 is an R and C++ program for fast genotype imputation from low-coverage sequence using a large reference panel. QUILT2 is accurate and versatile, able to handle imputation from ***short read, long read, ancient DNA and cell-free DNA from NIPT***.