3 citations · 4 across the 2 of their papers we have counts for
2 papers
cs.CE2014★ 3 cited
Fast and Scalable Inference of Multi-Sample Cancer Lineages
Victoria Popic, Raheleh Salari, Iman Hajirasouliha +3
Somatic variants can be used as lineage markers for the phylogenetic reconstruction of cancer evolution. Since somatic phylogenetics is complicated by sample heterogeneity, novel s…
q-bio.QM2010★ 1 cited
Pair HMM based gap statistics for re-evaluation of indels in alignments with affine gap penalties: Extended Version
Alexander Schönhuth, Raheleh Salari, S. Cenk Sahinalp
Although computationally aligning sequence is a crucial step in the vast majority of comparative genomics studies our understanding of alignment biases still needs to be improved.…