Prefix-free parsing for building big BWTs

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS

(2018) Clare Turnbull et al.   BMJ-British Medical Journal

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS

(2018) Clare Turnbull et al.   BMJ-British Medical Journal

Inducing enhanced suffix arrays for string collections

(2017) Felipe A. Louza et al.   THEORETICAL COMPUTER SCIENCE

The Public Health Impact of a Publically Available, Environmental Database of Microbial Genomes

(2017) Eric L. Stevens et al.   Frontiers in Microbiology

BCFtools/RoH: a hidden Markov model approach for detecting autozygosity from next-generation sequencing data

(2016) Vagheesh Narasimhan et al.   BIOINFORMATICS

The Metagenomics and Metadesign of the Subways and Urban Biomes (MetaSUB) International Consortium inaugural meeting report

(2016)   Microbiome

A global reference for human genetic variation

(2015) Richard A. Gibbs et al.   NATURE

Practical linear-timeO(1)-workspace suffix sorting for constant alphabets

(2013) Ge Nong   ACM TRANSACTIONS ON INFORMATION SYSTEMS

Fast gapped-read alignment with Bowtie 2

(2012) Ben Langmead et al.   NATURE METHODS

Lightweight Data Indexing and Compression in External Memory

(2011) Paolo Ferragina et al.   ALGORITHMICA

Fast and accurate long-read alignment with Burrows–Wheeler transform

(2010) Heng Li et al.   BIOINFORMATICS

SOAP2: an improved ultrafast tool for short read alignment

(2009) R. Li et al.   BIOINFORMATICS

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

(2009) Ben Langmead et al.   GENOME BIOLOGY