Ashley D Sanders

Computational pan-genomics: status, promises and challenges

Ying Zhang, Eleazar Eskin, Knut Reinert, 2016, bioRxiv.

breakpointR: an R/Bioconductor package to localize strand state changes in Strand-seq data

Victor Guryev, Maria Colomé-Tatché, David Porubsky, 2019, Bioinform..

Single-cell template strand sequencing by Strand-seq enables the characterization of individual homologs

Mark Hills, Ashley D Sanders, Peter M Lansdorp, 2017, Nature Protocols.

Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads

Aaron M Wenger, Carl Baker, Urvashi Surti, 2019, Annals of human genetics.

Dense and accurate whole-chromosome haplotyping of individual genomes

Victor Guryev, Tobias Marschall, Shilpa Garg, 2017, Nature Communications.

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Li Ding, Amina Noor, Ali Bashir, 2018, Nature Communications.

Direct chromosome-length haplotyping by single-cell sequencing

Victor Guryev, Mark Hills, Ashley D Sanders, 2016, Genome research.

Characterizing polymorphic inversions in human genomes by single-cell sequencing

Victor Guryev, Mark Hills, Ashley D Sanders, 2016, Genome research.