LevioSAM: fast lift-over of variant-aware reference alignments

por Mun, Taher, Chen, Nae-Chyun, Langmead, Ben
Publicado 2021

Pangenomic genotyping with the marker array

por Mun, Taher, Vaddadi, Naga Sai Kavya, Langmead, Ben
Publicado 2023

Pangenomic Genotyping with the Marker Array

por Mun, Taher, Vaddadi, Naga Sai Kavya, Langmead, Ben
Publicado 2022

Reference flow: reducing reference bias using multiple population genomes

por Chen, Nae-Chyun, Solomon, Brad, Mun, Taher, Iyer, Sheila, Langmead, Ben
Publicado 2021

Prefix-free parsing for building big BWTs

por Boucher, Christina, Gagie, Travis, Kuhnle, Alan, Langmead, Ben, Manzini, Giovanni, Mun, Taher
Publicado 2019

Matching Reads to Many Genomes with the r-Index

por Mun, Taher, Kuhnle, Alan, Boucher, Christina, Gagie, Travis, Langmead, Ben, Manzini, Giovanni
Publicado 2020

Efficient Construction of a Complete Index for Pan-Genomics Read Alignment

por Kuhnle, Alan, Mun, Taher, Boucher, Christina, Gagie, Travis, Langmead, Ben, Manzini, Giovanni
Publicado 2020